PIPERIDINYL-METHYLPURINE BENZENES AND RELATED COMPOUNDS AND THEIR USE IN TREATING DISEASES AND CONDITIONS CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application claims the benefit of U.S. Provisional Application No.63/344,794, filed on May 23, 2022, the entirety of which is hereby incorporated by reference. FIELD OF THE INVENTION [0002] The invention provides piperidinyl-methylpurine benzenes and related compounds, pharmaceutical compositions, their use for inhibiting NSD2, and their use in the treatment of a disease or condition, such as cancer. BACKGROUND [0003] Cancer continues to be a significant health problem despite the substantial research efforts and scientific advances reported in the literature for treating this disease. Solid tumors, including prostate cancer, breast cancer, and lung cancer remain highly prevalent among the world population. Current treatment options for these cancers are not effective for all patients and/or can have substantial adverse side effects. New therapies are needed to address this unmet need in cancer therapy. [0004] The nuclear receptor-binding SET domain protein 2 (NSD2), also known as multiple myeloma SET domain (MMSET) or Wolf-Hirschhorn syndrome candidate 1 (WHSC1), is an epigenetic modifier having a role in oncogenesis. Several human cancers are associated with NSD2 overexpression and/or activating point mutations. (Coussens et al., J. Biol. Chem. 293 (2018) 13750-13654.) For example, high expression of NSD2 has been reported in human cancers including bladder, brain, gastrointestinal, lung, liver, ovary, skin, uterus, breast, prostrate and glioblastoma. Additionally, pediatric cancer genomes appear to be particularly likely to contain NSD2 mutations. Finally, upregulation of NSD2 has been linked with aggressive tumor behavior and poor clinical outcomes. Certain compounds that inhibit NSD2 are described in international patent application publication WO 2021/028854. Additional compounds that inhibit NSD2 would be beneficial to patients suffering from an NSD2-related disease or condition. [0005] The present invention addresses the foregoing needs and provides other related advantages. SUMMARY [0006] The invention provides piperidinyl-methylpurine benzenes and related compounds, pharmaceutical compositions, their use for inhibiting NSD2, and their use in the treatment of a disease or condition, such as cancer. In particular, one aspect of the invention provides a collection of piperidinyl-methylpurine benzenes and related compounds, such as a compound represented by Formula I: (I) or a pharmaceutically acceptable salt thereof, where the variables are as defined in the detailed description. Further description of additional collections of piperidinyl-methylpurine benzenes and related compounds are described in the detailed description. The compounds may be part of a pharmaceutical composition comprising a pharmaceutically acceptable carrier. [0007] Another aspect of the invention provides a collection of piperidinyl-methylpurine pyridines and related compounds, such as a compound represented by Formula II: (II) or a pharmaceutically acceptable salt thereof, where the variables are as defined in the detailed description. Further description of additional collections of piperidinyl-methylpurine pyridines and related compounds are described in the detailed description. The compounds may be part of a pharmaceutical composition comprising a pharmaceutically acceptable carrier. [0008] Another aspect of the invention provides a method of treating a disease or condition mediated by NSD2 in a subject. The method comprises administering a therapeutically effective amount of a compound described herein, such as a compound of Formula I, I-A, II, or II-A, to a subject in need thereof to treat the disease or condition, as further described in the detailed description. [0009] Another aspect of the invention provides a method of inhibiting the activity of nuclear SET domain-containing protein 2 (NSD2). The method comprises contacting a NSD2 with an effective amount of a compound described herein, such as a compound of Formula I, I-A, II, or II-A, to inhibit the activity of said NSD2, as further described in the detailed description. DETAILED DESCRIPTION [0010] The invention provides piperidinyl-methylpurine benzenes and related compounds, pharmaceutical compositions, their use for inhibiting NSD2, and their use in the treatment of a disease or condition, such as cancer. The practice of the present invention employs, unless otherwise indicated, conventional techniques of organic chemistry, pharmacology, molecular biology (including recombinant techniques), cell biology, biochemistry, and immunology. Such techniques are explained in the literature, such as in “Comprehensive Organic Synthesis” (B.M. Trost & I. Fleming, eds., 1991-1992); “Handbook of experimental immunology” (D.M. Weir & C.C. Blackwell, eds.); “Current protocols in molecular biology” (F.M. Ausubel et al., eds., 1987, and periodic updates); and “Current protocols in immunology” (J.E. Coligan et al., eds., 1991), each of which is herein incorporated by reference in its entirety. [0011] Various aspects of the invention are set forth below in sections; however, aspects of the invention described in one particular section are not to be limited to any particular section. Further, when a variable is not accompanied by a definition, the previous definition of the variable controls. Definitions [0012] Compounds of the present invention include those described generally herein, and are further illustrated by the classes, subclasses, and species disclosed herein. As used herein, the following definitions shall apply unless otherwise indicated. These definitions apply regardless of whether a term is used by itself or in combination with other terms, unless otherwise indicated. Hence, the definition of “alkyl” applies to “alkyl” as well as the “alkyl” portions of “-O-alkyl” etc. For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75 ^th Ed. Additionally, general principles of organic chemistry are described in “Organic Chemistry”, Thomas Sorrell, University Science Books, Sausalito: 1999, and “March’s Advanced Organic Chemistry”, 5 ^th Ed., Ed.: Smith, M.B. and March, J., John Wiley & Sons, New York: 2001, the entire contents of which are hereby incorporated by reference. [0013] The term “aliphatic” or “aliphatic group”, as used herein, means a straight-chain (i.e., unbranched) or branched, substituted or unsubstituted hydrocarbon chain that is completely saturated or that contains one or more units of unsaturation, or a monocyclic hydrocarbon or bicyclic hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic (also referred to herein as “cycloaliphatic”), that has a single point of attachment to the rest of the molecule. Unless otherwise specified, aliphatic groups contain 1-6 aliphatic carbon atoms. In some embodiments, aliphatic groups contain 1-5 aliphatic carbon atoms. In other embodiments, aliphatic groups contain 1-4 aliphatic carbon atoms. In still other embodiments, aliphatic groups contain 1-3 aliphatic carbon atoms, and in yet other embodiments, aliphatic groups contain 1-2 aliphatic carbon atoms. In some embodiments, “cycloaliphatic” refers to a monocyclic C3-C6 hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic, that has a single point of attachment to the rest of the molecule. Suitable aliphatic groups include, but are not limited to, linear or branched, substituted or unsubstituted alkyl, alkenyl, alkynyl groups and hybrids thereof such as (cycloalkyl)alkyl, (cycloalkenyl)alkyl or (cycloalkyl)alkenyl. [0014] As used herein, the term “bicyclic ring” or “bicyclic ring system” refers to any bicyclic ring system, i.e., carbocyclic or heterocyclic, saturated or having one or more units of unsaturation, having one or more atoms in common between the two rings of the ring system. Thus, the term includes any permissible ring fusion, such as ortho-fused or spirocyclic. As used herein, the term “heterobicyclic” is a subset of “bicyclic” that requires that one or more heteroatoms are present in one or both rings of the bicycle. Such heteroatoms may be present at ring junctions and are optionally substituted, and may be selected from nitrogen (including N-oxides), oxygen, sulfur (including oxidized forms such as sulfones and sulfonates), phosphorus (including oxidized forms such as phosphates), boron, etc. In some embodiments, a bicyclic group has 7-12 ring members and 0-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur. As used herein, the term “bridged bicyclic” refers to any bicyclic ring system, i.e., carbocyclic or heterocyclic, saturated or partially unsaturated, having at least one bridge. As defined by IUPAC, a “bridge” is an unbranched chain of atoms or an atom or a valence bond connecting two bridgeheads, where a “bridgehead” is any skeletal atom of the ring system which is bonded to three or more skeletal atoms (excluding hydrogen). In some embodiments, a bridged bicyclic group has 7-12 ring members and 0-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur. Such bridged bicyclic groups are well known in the art and include those groups set forth below where each group is attached to the rest of the molecule at any substitutable carbon or nitrogen atom. Unless otherwise specified, a bridged bicyclic group is optionally substituted with one or more substituents as set forth for aliphatic groups. Additionally or alternatively, any substitutable nitrogen of a bridged bicyclic group is optionally substituted. Exemplary bicyclic rings include: [0015] Exemplary bridged bicyclics include:

[0016] The term “lower alkyl” refers to a C _1-4 straight or branched alkyl group. Exemplary lower alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, and tert-butyl. [0017] The term “lower haloalkyl” refers to a C _1-4 straight or branched alkyl group that is substituted with one or more halogen atoms. [0018] The term “heteroatom” means one or more of oxygen, sulfur, nitrogen, phosphorus, or silicon (including, any oxidized form of nitrogen, sulfur, phosphorus, or silicon; the quaternized form of any basic nitrogen or; a substitutable nitrogen of a heterocyclic ring, for example N (as in 3,4-dihydro-2H-pyrrolyl), NH (as in pyrrolidinyl) or NR ⁺ (as in N-substituted pyrrolidinyl)). [0019] The term “unsaturated,” as used herein, means that a moiety has one or more units of unsaturation. [0020] As used herein, the term “bivalent C _1-8 (or C _1-6 ) saturated or unsaturated, straight or branched, hydrocarbon chain”, refers to bivalent alkylene, alkenylene, and alkynylene chains that are straight or branched as defined herein. [0021] The term “alkylene” refers to a bivalent alkyl group. An “alkylene chain” is a polymethylene group, i.e., –(CH ₂ ) _n –, wherein n is a positive integer, preferably from 1 to 6, from 1 to 4, from 1 to 3, from 1 to 2, or from 2 to 3. A substituted alkylene chain is a polymethylene group in which one or more methylene hydrogen atoms are replaced with a substituent. Suitable substituents include those described below for a substituted aliphatic group. [0022] The term “-(C ₀ alkylene)-“ refers to a bond. Accordingly, the term “-(C _0-3 alkylene)-” encompasses a bond (i.e., C ₀ ) and a -(C _1-3 alkylene)- group. [0023] The term “alkenylene” refers to a bivalent alkenyl group. A substituted alkenylene chain is a polymethylene group containing at least one double bond in which one or more hydrogen atoms are replaced with a substituent. Suitable substituents include those described below for a substituted aliphatic group. [0024] The term “halogen” means F, C1, Br, or I. [0025] The term “aryl” used alone or as part of a larger moiety as in “aralkyl,” “aralkoxy,” or “aryloxyalkyl,” refers to monocyclic or bicyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic and wherein each ring in the system contains 3 to 7 ring members. The term “aryl” may be used interchangeably with the term “aryl ring.” In certain embodiments of the present invention, “aryl” refers to an aromatic ring system which includes, but not limited to, phenyl, biphenyl, naphthyl, anthracyl and the like, which may bear one or more substituents. Also included within the scope of the term “aryl,” as it is used herein, is a group in which an aromatic ring is fused to one or more non–aromatic rings, such as indanyl, phthalimidyl, naphthimidyl, phenanthridinyl, or tetrahydronaphthyl, and the like. The term “phenylene” refers to a multivalent phenyl group having the appropriate number of open valences to account for groups attached to it. For example, “phenylene” is a bivalent phenyl group when it has two groups attached to it (e.g., “phenylene” is a trivalent phenyl group when it has three groups attached to it (e.g., . The term “arylene” refers to a bivalent aryl group. [0026] The terms “heteroaryl” and “heteroar–,” used alone or as part of a larger moiety, e.g., “heteroaralkyl,” or “heteroaralkoxy,” refer to groups having 5 to 10 ring atoms, preferably 5, 6, or 9 ring atoms; having 6, 10, or 14 π electrons shared in a cyclic array; and having, in addition to carbon atoms, from one to five heteroatoms. The term “heteroatom” refers to nitrogen, oxygen, or sulfur, and includes any oxidized form of nitrogen or sulfur, and any quaternized form of a basic nitrogen. Heteroaryl groups include, without limitation, thienyl, furanyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, indolizinyl, purinyl, naphthyridinyl, and pteridinyl. The terms “heteroaryl” and “heteroar–”, as used herein, also include groups in which a heteroaromatic ring is fused to one or more aryl, cycloaliphatic, or heterocyclyl rings, where unless otherwise specified, the radical or point of attachment is on the heteroaromatic ring or on one of the rings to which the heteroaromatic ring is fused Nonlimiting examples include indolyl isoindolyl, benzothienyl, benzofuranyl, dibenzofuranyl, indazolyl, benzimidazolyl, benzthiazolyl, quinolyl, isoquinolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 4H–quinolizinyl, carbazolyl, acridinyl, phenazinyl, phenothiazinyl, phenoxazinyl, tetrahydroquinolinyl, and tetrahydroisoquinolinyl. A heteroaryl group may be mono– or bicyclic. The term “heteroaryl” may be used interchangeably with the terms “heteroaryl ring,” “heteroaryl group,” or “heteroaromatic,” any of which terms include rings that are optionally substituted. The term “heteroaralkyl” refers to an alkyl group substituted by a heteroaryl, wherein the alkyl and heteroaryl portions independently are optionally substituted. [0027] The term “heteroarylene” refers to a multivalent heteroaryl group having the appropriate number of open valences to account for groups attached to it. For example, “heteroarylene” is a bivalent heteroaryl group when it has two groups attached to it; “heteroarylene” is a trivalent heteroaryl group when it has three groups attached to it. The term “pyridinylene” refers to a multivalent pyridine radical having the appropriate number of open valences to account for groups attached to it. For example, “pyridinylene” is a bivalent pyridine radical when it has two groups attached to it (e.g., ); “pyridinylene” is a trivalent pyridine radical when it has three groups attached to it (e.g., ). [0028] As used herein, the terms “heterocycle,” “heterocyclyl,” “heterocyclic radical,” and “heterocyclic ring” are used interchangeably and refer to a stable 5– to 7–membered monocyclic or 7–10–membered bicyclic heterocyclic moiety that is either saturated or partially unsaturated, and having, in addition to carbon atoms, one or more, preferably one to four, heteroatoms, as defined above. When used in reference to a ring atom of a heterocycle, the term "nitrogen" includes a substituted nitrogen. As an example, in a saturated or partially unsaturated ring having 0–3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3,4–dihydro– 2H–pyrrolyl), NH (as in pyrrolidinyl), or ⁺ NR (as in N–substituted pyrrolidinyl). [0029] A heterocyclic ring can be attached to its pendant group at any heteroatom or carbon atom that results in a stable structure and any of the ring atoms can be optionally substituted. Examples of such saturated or partially unsaturated heterocyclic radicals include, without limitation, tetrahydrofuranyl, tetrahydrothiophenyl pyrrolidinyl, piperidinyl, pyrrolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, decahydroquinolinyl, oxazolidinyl, piperazinyl, dioxanyl, dioxolanyl, diazepinyl, oxazepinyl, thiazepinyl, morpholinyl, 2-oxa-6-azaspiro[3.3]heptane, and quinuclidinyl. The terms “heterocycle,” “heterocyclyl,” “heterocyclyl ring,” “heterocyclic group,” “heterocyclic moiety,” and “heterocyclic radical,” are used interchangeably herein, and also include groups in which a heterocyclyl ring is fused to one or more aryl, heteroaryl, or cycloaliphatic rings, such as indolinyl, 3H–indolyl, chromanyl, phenanthridinyl, or tetrahydroquinolinyl. A heterocyclyl group may be mono– or bicyclic. The term “heterocyclylalkyl” refers to an alkyl group substituted by a heterocyclyl, wherein the alkyl and heterocyclyl portions independently are optionally substituted. The term “oxo-heterocyclyl” refers to a heterocyclyl substituted by an oxo group. The term “heterocyclylene” refers to a multivalent heterocyclyl group having the appropriate number of open valences to account for groups attached to it. For example, “heterocyclylene” is a bivalent heterocyclyl group when it has two groups attached to it; “heterocyclylene” is a trivalent heterocyclyl group when it has three groups attached to it. [0030] As used herein, the term “partially unsaturated” refers to a ring moiety that includes at least one double or triple bond. The term “partially unsaturated” is intended to encompass rings having multiple sites of unsaturation, but is not intended to include aryl or heteroaryl moieties, as herein defined. [0031] As described herein, compounds of the invention may contain “optionally substituted” moieties. In general, the term “substituted,” whether preceded by the term “optionally” or not, means that one or more hydrogens of the designated moiety are replaced with a suitable substituent. Unless otherwise indicated, an “optionally substituted” group may have a suitable substituent at each substitutable position of the group, and when more than one position in any given structure may be substituted with more than one substituent selected from a specified group, the substituent may be either the same or different at every position. Combinations of substituents envisioned by this invention are preferably those that result in the formation of stable or chemically feasible compounds. The term “stable,” as used herein, refers to compounds that are not substantially altered when subjected to conditions to allow for their production, detection, and, in certain embodiments, their recovery, purification, and use for one or more of the purposes disclosed herein. [0032] Each optional substituent on a substitutable carbon is a monovalent substituent independently selected from halogen; –(CH ₂ ) _0–4 R º; –(CH ₂ ) _0–4 OR º; -O(CH ₂ ) _0-4 R ^o , –O–(CH ₂ )0– 4C(O)OR°; –(CH ₂ ) _0-4 CH(OR°) ₂ ; –(CH ₂ ) _0-4 SR ^o ; –(CH ₂ ) _0-4 Ph, which may be substituted with R°; –(CH ₂ ) _0-4 O(CH ₂ ) _0–1 Ph which may be substituted with R°; –CH=CHPh, which may be substituted with R°; –(CH ₂ ) _0-4 O(CH ₂ ) _0–1 -pyridyl which may be substituted with R°; –NO ₂ ; –CN; – N ₃ ; -(CH ₂ ) _0–4 N(R ^o ) ₂ ; –(CH ₂ ) _0–4 N(R ^o )C(O)R ^o ; –N(R ^o )C(S)R ^o ; –(CH ₂ ) _0–4 N(R ^o )C(O)NR ^o ₂ ; -N(R ^o )C(S)NR ^o ₂ ; –(CH ₂ ) _0–4 N(R ^o )C(O)OR°; –N(R ^o )N(R ^o )C(O)R ^o ; -N(R ^o )N(R ^o )C(O)NR ^o ₂ ; -N(R ^o )N(R ^o )C(O)OR°; –(CH ₂ ) _0–4 C(O)R ^o ; –C(S)R ^o ; –(CH ₂ ) _0–4 C(O)OR°; –(CH ₂ ) _0–4 C(O)SR ^o ; -(CH ₂ ) _0–4 C(O)OSiR ^o ₃ ; –(CH ₂ ) _0–4 OC(O)R ^o ; –OC(O)(CH ₂ ) _0–4 SR–, SC(S)SR°; –(CH ₂ ) _0–4 SC(O)R ^o ; –(CH ₂ ) _0-4 C(O)NR ^o ₂ ; –C(S)NR ^o ₂ ; –C(S)SR°; –SC(S)SR°, -(CH ₂ ) _0-4 OC(O)NR ^o ₂ ; -C(O)N(OR°)R ^o ; –C(O)C(O)R ^o ; –C(O)CH ₂ C(O)R ^o ; –C(NOR°)R ^o ; -(CH ₂ ) _0-4 SSR ^o ; –(CH ₂ )0– 4S(O) ₂ R ^o ; –(CH ₂ ) _0-4 S(O) ₂ OR°; –(CH ₂ ) _0-4 OS(O) ₂ R ^o ; –S(O) ₂ NR ^o ₂ ; –S(O)(NR ^o )R ^o ; – S(O) ₂ N=C(NR ^o ₂ ) ₂ ; -(CH ₂ ) _0-4 S(O)R ^o ; -N(R ^o )S(O) ₂ NR ^o ₂ ; –N(R ^o )S(O) ₂ R ^o ; –N(OR°)R ^o ; – C(NH)NR ^o ₂ ; –P(O) ₂ R ^o ; -P(O)R ^o ₂ ; -OP(O)R ^o ₂ ; –OP(O)(OR°) ₂ ; SiR ^o 3; –(C1–4 straight or branched alkylene)O–N(R ^o ) ₂ ; or –(C _1–4 straight or branched alkylene)C(O)O–N(R ^o ) ₂ . [0033] Each R ^o is independently hydrogen, C _1–6 aliphatic, –CH ₂ Ph, –O(CH ₂ ) _0–1 Ph, -CH ₂ -(5-6 membered heteroaryl ring), or a 5–6–membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, or, notwithstanding the definition above, two independent occurrences of R ^o , taken together with their intervening atom(s), form a 3–12–membered saturated, partially unsaturated, or aryl mono– or bicyclic ring having 0– 4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, which may be substituted by a divalent substituent on a saturated carbon atom of R ^o selected from =O and =S; or each R ^o is optionally substituted with a monovalent substituent independently selected from halogen, – (CH ₂ ) _0–2 R ^▪ , –(haloR ^▪ ), –(CH ₂ ) _0–2 OH, –(CH ₂ ) _0–2 OR ^▪ , –(CH ₂ ) _0–2 CH(OR ^▪ ) ₂ ; -O(haloR ^▪ ), –CN, –N ₃ , –(CH ₂ ) _0–2 C(O)R ^▪ , –(CH ₂ ) _0–2 C(O)OH, –(CH ₂ ) _0–2 C(O)OR ^▪ , –(CH ₂ ) _0–2 SR ^▪ , –(CH ₂ ) _0–2 SH, –(CH ₂ ) _{0– 2} NH ₂ , –(CH ₂ )0– ₂ NHR ^▪ , –(CH ₂ )0– ₂ NR ^▪ ₂ , –NO ₂ , –SiR ^▪ ₃ , –OSiR ^▪ ₃ , -C(O)SR ^▪ , –(C _1–4 straight or branched alkylene)C(O)OR ^▪ , or –SSR ^▪ . [0034] Each R ^▪ is independently selected from C _1–4 aliphatic, –CH ₂ Ph, –O(CH ₂ ) _0–1 Ph, or a 5–6– membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, and wherein each R ^▪ is unsubstituted or where preceded by halo is substituted only with one or more halogens; or wherein an optional substituent on a saturated carbon is a divalent substituent independently selected from =O, =S, =NNR ^* ₂ , =NNHC(O)R ^* , =NNHC(O)OR ^* , =NNHS(O) ₂ R ^* , =NR ^* , =NOR ^* , –O(C(R ^* ₂ )) _2–3 O–, or – S(C(R ^* ₂ )) _2–3 S–, or a divalent substituent bound to vicinal substitutable carbons of an “optionally substituted” group is –O(CR ^* ₂ ) _2–3 O–, wherein each independent occurrence of R ^* is selected from hydrogen, C _1–6 aliphatic or an unsubstituted 5–6–membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur. [0035] When R ^* is C _1–6 aliphatic, R ^* is optionally substituted with halogen, –R ^▪ , -(haloR ^▪ ), -OH, –OR ^▪ , –O(haloR ^▪ ), –CN, –C(O)OH, –C(O)OR ^▪ , –NH ₂ , –NHR ^▪ , –NR ^▪ ₂ , or –NO ₂ , wherein each R ^▪ is independently selected from C _1–4 aliphatic, –CH ₂ Ph, –O(CH ₂ ) _0–1 Ph, or a 5–6–membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, and wherein each R ^▪ is unsubstituted or where preceded by halo is substituted only with one or more halogens. [0036] An optional substituent on a substitutable nitrogen is independently –R ^† , –NR ^† ₂ , –C(O)R ^† , –C(O)OR ^† , –C(O)C(O)R ^† , –C(O)CH ₂ C(O)R ^† , -S(O) ₂ R ^† , -S(O) ₂ NR ^† ₂ , –C(S)NR ^† ₂ , –C(NH)NR ^† ₂ , or –N(R ^† )S(O) ₂ R ^† ; wherein each R ^† is independently hydrogen, C _1–6 aliphatic, unsubstituted –OPh, or an unsubstituted 5–6–membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, or, two independent occurrences of R ^† , taken together with their intervening atom(s) form an unsubstituted 3–12– membered saturated, partially unsaturated, or aryl mono– or bicyclic ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur; wherein when R ^† is C _1–6 aliphatic, R ^† is optionally substituted with halogen, –R ^▪ , -(haloR ^▪ ), -OH, –OR ^▪ , –O(haloR ^▪ ), –CN, –C(O)OH, – C(O)OR ^▪ , –NH ₂ , –NHR ^▪ , –NR ^▪ ₂ , or –NO ₂ , wherein each R ^▪ is independently selected from C _{1– 4} aliphatic, –CH ₂ Ph, –O(CH ₂ ) _0–1 Ph, or a 5–6–membered saturated, partially unsaturated, or aryl ring having 0–4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, and wherein each R ^▪ is unsubstituted or where preceded by halo is substituted only with one or more halogens. [0037] As used herein, the term "pharmaceutically acceptable salt" refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge et al., describe pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 1977, 66, 1–19, incorporated herein by reference. Pharmaceutically acceptable salts of the compounds of this invention include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2– hydroxy–ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2–naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3–phenylpropionate, phosphate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p–toluenesulfonate, undecanoate, valerate salts, and the like. [0038] Further, acids which are generally considered suitable for the formation of pharmaceutically useful salts from basic pharmaceutical compounds are discussed, for example, by P. Stahl et al., Camille G. (eds.) Handbook of Pharmaceutical Salts. Properties, Selection and Use. (2002) Zurich: Wiley-VCH; S. Berge et al., Journal of Pharmaceutical Sciences (1977) 66(1) 1-19; P. Gould, International J. of Pharmaceutics (1986) 33 201-217; Anderson et al., The Practice of Medicinal Chemistry (1996), Academic Press, New York; and in The Orange Book (Food & Drug Administration, Washington, D.C. on their website). These disclosures are incorporated herein by reference. [0039] Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N ⁺ (C _1–4 alkyl) ₄ salts. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate. [0040] Unless otherwise stated, structures depicted herein are also meant to include all isomeric (e.g., enantiomeric, diastereomeric, and geometric (or conformational)) forms of the structure; for example, the R and S configurations for each asymmetric center, Z and E double bond isomers, and Z and E conformational isomers. Therefore, single stereochemical isomers as well as enantiomeric, diastereomeric, and geometric (or conformational) mixtures of the present compounds are within the scope of the invention. Unless otherwise stated, all tautomeric forms of the compounds of the invention are within the scope of the invention. The invention includes compounds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures including the replacement of hydrogen by deuterium or tritium, or the replacement of a carbon by a ¹³ C- or ¹⁴ C-enriched carbon are within the scope of this invention. Such compounds are useful, for example, as analytical tools, as probes in biological assays, or as therapeutic agents in accordance with the present invention. [0041] Diastereomeric mixtures can be separated into their individual diastereomers on the basis of their physical chemical differences by methods known to those skilled in the art, such as, for example, by chromatography and/or fractional crystallization. Enantiomers can be separated by converting the enantiomeric mixture into a diastereomeric mixture by reaction with an appropriate optically active compound (e.g., chiral auxiliary such as a chiral alcohol or Mosher’s acid chloride), separating the diastereomers and converting (e.g., hydrolyzing) the individual diastereomers to the corresponding pure enantiomers. Alternatively, a particular enantiomer of a compound of the present invention may be prepared by asymmetric synthesis. Still further, where the molecule contains a basic functional group (such as amino) or an acidic functional group (such as carboxylic acid) diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional crystallization or chromatographic means known in the art, and subsequent recovery of the pure enantiomers. [0042] Individual stereoisomers of the compounds of the invention may, for example, be substantially free of other isomers, or may be admixed, for example, as racemates or with all other, or other selected, stereoisomers. Chiral center(s) in a compound of the present invention can have the S or R configuration as defined by the IUPAC 1974 Recommendations. Further, to the extent a compound described herein may exist as an atropisomer (e.g., substituted biaryls), all forms of such atropisomer are considered part of this invention. [0043] Chemical names, common names, and chemical structures may be used interchangeably to describe the same structure. If a chemical compound is referred to using both a chemical structure and a chemical name, and an ambiguity exists between the structure and the name, the structure predominates. It should also be noted that any carbon as well as heteroatom with unsatisfied valences in the text, schemes, examples and tables herein is assumed to have the sufficient number of hydrogen atom(s) to satisfy the valences. [0044] Unless specified otherwise, the term “about” refers to within ±10% of the stated value. The invention encompasses embodiments where the value is within ±9%, ±8%, ±7%, ±6%, ±5%, ±4%, ±3%, ±2%, or ±1% of the stated value. [0045] The terms “a” and “an” as used herein mean “one or more” and include the plural unless the context is inappropriate. [0046] The term “alkyl” refers to a saturated straight or branched hydrocarbon, such as a straight or branched group of 1-12, 1-10, or 1-6 carbon atoms, referred to herein as C ₁ -C ₁₂ alkyl, C ₁ -C ₁₀ alkyl, and C ₁ -C ₆ alkyl, respectively. Exemplary alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, 2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3- methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2,2-dimethyl-1- butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, octyl, etc. [0047] The term “cycloalkyl” refers to a monovalent saturated cyclic, bicyclic, or bridged cyclic (e.g., adamantyl) hydrocarbon group of 3-12, 3-8, 4-8, or 4-6 carbons, referred to herein, e.g., as “C ₃ -C ₆ cycloalkyl,” derived from a cycloalkane. Exemplary cycloalkyl groups include cyclohexyl, cyclopentyl, cyclobutyl, and cyclopropyl. The term “cycloalkylene” refers to a bivalent cycloalkyl group. [0048] The term “haloalkyl” refers to an alkyl group that is substituted with at least one halogen. Exemplary haloalkyl groups include -CH ₂ F, -CHF ₂ , -CF3, -CH ₂ CF ₃ , -CF ₂ CF ₃ , and the like. The term “haloalkylene” refers to a bivalent haloalkyl group. [0049] The terms “alkenyl” and “alkynyl” are art-recognized and refer to unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but that contain at least one double or triple bond respectively. [0050] The terms “alkoxyl” or “alkoxy” are art-recognized and refer to an alkyl group, as defined above, having an oxygen radical attached thereto. Representative alkoxyl groups include methoxy, ethoxy, propyloxy, tert-butoxy and the like. The term “haloalkoxyl” refers to an alkoxyl group that is substituted with at least one halogen. Exemplary haloalkoxyl groups include -OCH ₂ F, - OCHF ₂ , -OCF ₃ , -OCH ₂ CF ₃ , -OCF ₂ CF ₃ , and the like. The term “hydroxyalkoxyl” refers to an alkoxyl group that is substituted with at least one hydroxyl. Exemplary hydroxyalkoxyl groups include -OCH ₂ CH ₂ OH, -OCH ₂ C(H)(OH)CH ₂ CH ₂ OH, and the like. The term “alkoxylene” refers to a bivalent alkoxyl group. [0051] The term “oxo” is art-recognized and refers to a “=O” substituent. For example, a cyclopentane substituted with an oxo group is cyclopentanone. [0052] The symbol “ ” indicates a point of attachment. [0053] When any substituent or variable occurs more than one time in any constituent or the compound of the invention, its definition on each occurrence is independent of its definition at every other occurrence, unless otherwise indicated. [0054] One or more compounds of the invention may exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like, and it is intended that the invention embrace both solvated and unsolvated forms. “Solvate” means a physical association of a compound of this invention with one or more solvent molecules. This physical association involves varying degrees of ionic and covalent bonding, including hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid. “Solvate” encompasses both solution-phase and isolatable solvates. Non-limiting examples of suitable solvates include ethanolates, methanolates, and the like. “Hydrate” is a solvate wherein the solvent molecule is H ₂ O. [0055] As used herein, the terms “subject” and “patient” are used interchangeably and refer to organisms to be treated by the methods of the present invention. Such organisms preferably include, but are not limited to, mammals (e.g., murines, simians, equines, bovines, porcines, canines, felines, and the like), and, most preferably, includes humans. [0056] As used herein, the term "compound" refers to a quantity of molecules that is sufficient to be weighed, tested for its structural identity, and to have a demonstrable use (e.g., a quantity that can be shown to be active in an assay, an in vitro test, or in vivo test, or a quantity that can be administered to a patient and provide a therapeutic benefit). [0057] The term “IC ₅₀ ” is art-recognized and refers to the concentration of a compound that is required to achieve 50% inhibition of the target. [0058] As used herein, the term “effective amount” refers to the amount of a compound sufficient to effect beneficial or desired results (e.g., a therapeutic, ameliorative, inhibitory, or preventative result). An effective amount can be administered in one or more administrations, applications, or dosages and is not intended to be limited to a particular formulation or administration route. [0059] As used herein, the term “treating” includes any effect, e.g., lessening, reducing, modulating, ameliorating or eliminating, that results in the improvement of the condition, disease, disorder, and the like, or ameliorating a symptom thereof. [0060] As used herein, the term “pharmaceutical composition” refers to the combination of an active agent with a carrier, inert or active, making the composition especially suitable for diagnostic or therapeutic use in vivo or ex vivo. [0061] As used herein, the term “pharmaceutically acceptable carrier” refers to any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, emulsions (e.g., such as an oil/water or water/oil emulsions), and various types of wetting agents. The compositions also can include stabilizers and preservatives. For examples of carriers, stabilizers and adjuvants, see e.g., Martin, Remington’s Pharmaceutical Sciences, 15th Ed., Mack Publ. Co., Easton, PA [1975]. [0062] Throughout the description, where compositions are described as having, including, or comprising specific components, or where processes and methods are described as having, including, or comprising specific steps, it is contemplated that, additionally, there are compositions of the present invention that consist essentially of, or consist of, the recited components, and that there are processes and methods according to the present invention that consist essentially of, or consist of, the recited processing steps. [0063] As a general matter, compositions specifying a percentage are by weight unless otherwise specified. I. Piperidinyl-Methylpurine Benzenes and Related Compounds [0064] The invention provides piperidinyl-methylpurine benzenes and related compounds. The compounds may be used in the pharmaceutical compositions and therapeutic methods described herein. Exemplary compounds are described in the following sections, along with exemplary procedures for making the compounds. [0065] One aspect of the invention provides a compound represented by Formula I: (I) or a pharmaceutically acceptable salt thereof; wherein: R ¹ is selected from the group consisting of: a.C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen; R ^1A and R ⁷ each represents independently for each occurrence halo,C _1-6 alkyl,C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl; R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ ; R ^3A and R ^3B each represents independently hydrogen or C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring; R ^3C isC _1-6 alkyl or hydrogen; R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 47 membered saturated ring having one nitrogen atom; R ⁵ and R ⁶ each represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl,C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano; Ring A is phenylene, ; each of which is substituted with q occurrences of R ⁷ , wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² ; m and n are each independently 0, 1, 2, or 3; and p and q are each independently 0, 1, or 2. [0066] The definitions of variables in Formula I above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition of a variable is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii). [0067] In certain embodiments, the compound is a compound of Formula I. [0068] As defined generally above, R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen. [0069] In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl. In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 1 occurrence of hydroxyl. In certain embodiments, R ¹ is or In certain embodiments, R ¹ is -CH ₂ CHF ₂ . [0070] In certain embodiments, R ¹ is -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)OR ^3C . In certain embodiments, R ¹ is - C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)-(C _1-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)- (C _3-7 cycloalkyl). [0071] In certain embodiments, R ¹ is -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridinyl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridin-2-yl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is [0072] In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms), wherein said heteroaryl is substituted with m occurrences of R ⁵ . [0073] In certain embodiments, R ¹ is hydrogen. In certain embodiments, R ¹ is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0074] As defined generally above, R ^1A represents independently for each occurrence halo, C _1-6 alkyl, C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl. In certain embodiments, R ^1A represents independently for each occurrence halo, C _1-6 alkyl, or C _1-6 haloalkyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkyl or C _1-6 haloalkyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkoxyl or hydroxyl. [0075] In certain embodiments, R ^1A represents independently for each occurrence halo. In certain embodiments, R ^1A represents independently for each occurrence fluoro or chloro. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ^1A is methyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 haloalkyl. In certain embodiments, R ^1A is trifluoromethyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkoxyl. In certain embodiments, R ^1A is methoxy. In certain embodiments, R ^1A is hydroxyl. In certain embodiments, R ^1A is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0076] As defined generally above, R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ . [0077] In certain embodiments, R ² is phenyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is In certain embodiments, R ² is In certain embodiments, R ² is In certain embodiments, R ² is [0078] In certain embodiments, R ² is . In certain embodiments, R ² is In certain embodiments, R ² is . In certain embodiments, R ² i ² In certain embodiments, R [0079] In certain embodiments, R ² is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridinyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridin-2-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is [0080] In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazolyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazol-5-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² [0081] In certain embodiments, R ² is C _3-7 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-5 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is cyclopropyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-7 cycloalkyl. In certain embodiments, R ² is C _3-5 cycloalkyl. In certain embodiments, R ² is cyclopropyl. [0082] In certain embodiments, R ² is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0083] As defined generally above, R ^3A and R ^3B each represents independently hydrogen or C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. [0084] In certain embodiments, R ^3A and R ^3B each represents independently hydrogen or C _1-4 alkyl. In certain embodiments, R ^3A and R ^3B each represents independently hydrogen or methyl. In certain embodiments, R ^3A is hydrogen and R ^3B is methyl. In certain embodiments, R ^3A and R ^3B are hydrogen. In certain embodiments, R ^3A and R ^3B are methyl. In certain embodiments, R ^3A and R ^3B are taken together to represent oxo. [0085] In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-5 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a cyclopropane ring. [0086] In certain embodiments, R ^3A and R ^3B are selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0087] As defined generally above, R ^3C is C _1-6 alkyl or hydrogen. In certain embodiments, R ^3C is C _1-6 alkyl. In certain embodiments, R ^3C is C _1-4 alkyl. In certain embodiments, R ^3C is methyl. In certain embodiments, R ^3C is hydrogen. In certain embodiments, R ^3C is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0088] As defined generally above, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. [0089] In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence methyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁴ is methyl. In certain embodiments, R ⁴ is hydrogen. [0090] In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 5-6 membered saturated ring having one nitrogen atom. [0091] In certain embodiments, R ⁴ is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0092] As defined generally above, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0093] In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁵ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0094] In certain embodiments, R ⁵ represents independently for each occurrence halo. In certain embodiments, R ⁵ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁵ is methyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁵ is trifluoromethyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁵ is methoxy. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁵ is hydroxyl. In certain embodiments, R ⁵ is cyano. [0095] In certain embodiments, R ⁵ is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0096] As defined generally above, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0097] In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁶ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0098] In certain embodiments, R ⁶ represents independently for each occurrence halo. In certain embodiments, R ⁶ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁶ is methyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁶ is trifluoromethyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁶ is methoxy. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁶ is hydroxyl. In certain embodiments, R ⁶ is cyano. [0099] In certain embodiments, R ⁶ is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0100] As defined generally above, R ⁷ represents independently for each occurrence halo, C _1-6 alkyl, C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl. In certain embodiments, R ⁷ represents independently for each occurrence halo, C _1-6 alkyl, or C _1-6 haloalkyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkyl or C _1-6 haloalkyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkoxyl or hydroxyl. [0101] In certain embodiments, R ⁷ represents independently for each occurrence halo. In certain embodiments, R ⁷ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁷ is methyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 haloalkyl. In certain embodiments, R ⁷ is trifluoromethyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkoxyl. In certain embodiments, R ⁷ is methoxy. In certain embodiments, R ⁷ is hydroxyl. In certain embodiments, R ⁷ is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0102] As defined generally above, Ring A is phenylene, ; each of which 7 is substituted with q occurrences of R , wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² . In certain embodiments, Ring A is phenylene substituted with q occurrences of R ⁷ . In certain embodiments, Ring A is substituted with q occurrences of R ⁷ . In certain embodiments, Ring A is substituted with q occurrences of R ⁷ . In certain embodiments, Ring A is substituted with q occurrences of R ⁷ . [0103] In certain embodiments, Ring A is phenylene. In certain embodiments, Ring A is In certain embodiments, Ring A is In certain embodiments, Ring A is In certain embodiments, Ring A is selected from the groups depicted in the compounds in Tables 1, 2, and 3, below. [0104] As defined generally above, m is 0, 1, 2, or 3. In certain embodiments, m is 0. In certain embodiments, m is 1. In certain embodiments, m is 2. In certain embodiments, m is 3. In certain embodiments, m is 0 or 1. In certain embodiments, m is 1 or 2. In certain embodiments, m is 2 or 3. In certain embodiments, m is 0, 1, or 2. In certain embodiments, m is 1, 2, or 3. In certain embodiments, m is selected from the values represented in the compounds in Tables 1, 2, and 3, below. [0105] As defined generally above, n is 0, 1, 2, or 3. In certain embodiments, n is 0. In certain embodiments, n is 1. In certain embodiments, n is 2. In certain embodiments, n is 3. In certain embodiments, n is 0 or 1. In certain embodiments, n is 1 or 2. In certain embodiments, n is 2 or 3. In certain embodiments, n is 0, 1, or 2. In certain embodiments, n is 1, 2, or 3. In certain embodiments, n is selected from the values represented in the compounds in Tables 1, 2, and 3, below. [0106] As defined generally above, p is 0, 1 or 2. In certain embodiments, p is 0. In certain embodiments, p is 1. In certain embodiments, p is 2. In certain embodiments, p is 0 or 1. In certain embodiments, p is 1 or 2. In certain embodiments, p is selected from the values represented in the compounds in Tables 1, 2, and 3, below. [0107] In certain embodiments, p and q are 0. [0108] As defined generally above, q is 0, 1 or 2. In certain embodiments, q is 0. In certain embodiments, q is 1. In certain embodiments, q is 2. In certain embodiments, q is 0 or 1. In certain embodiments, q is 1 or 2. In certain embodiments, q is selected from the values represented in the compounds in Tables 1, 2, and 3, below. [0109] The description above describes multiple embodiments relating to compounds of Formula I. The patent application specifically contemplates all combinations of the embodiments. [0110] Another aspect of the invention provides a compound represented by Formula I-A: (I-A) or a pharmaceutically acceptable salt thereof; wherein: R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen; R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ ; R ^3C is C _1-6 alkyl or hydrogen; R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom; R ⁵ and R ⁶ each represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano; Ring A is ; wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² ; and m and n are each independently 0, 1, 2, or 3. [0111] The definitions of variables in Formula I-A above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition of a variable is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii). [0112] In certain embodiments, the compound is a compound of Formula I-A. [0113] As defined generally above, R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen. [0114] In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl. In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 1 2, or 3 halo, and (ii) 1 occurrence of hydroxyl. In certain embodiments, R is or . In certain embodiments, R ¹ is -CH ₂ CHF ₂ . [0115] In certain embodiments, R ¹ is -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)OR ^3C . In certain embodiments, R ¹ is - C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)-(C _1-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)- (C _3-7 cycloalkyl). [0116] In certain embodiments, R ¹ is -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridinyl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridin-2-yl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is [0117] In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms), wherein said heteroaryl is substituted with m occurrences of R ⁵ . [0118] In certain embodiments, R ¹ is hydrogen. [0119] As defined generally above, R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ . [0120] In certain embodiments, R ² is phenyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is . In c ² ertain embodiments, R is In certain embodiments, R ² is In certain embodiments, R ² is [0121] In certain embodiments, R ² is . In certain embodiments, R ² is . In certain embodiments, R ² is . In certain embodiments, R ² is In certain embodiments, R ² is [0122] In certain embodiments, R ² is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridinyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridin-2-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is . [0123] In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazolyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazol-5-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is [0124] In certain embodiments, R ² is C _3-7 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-5 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is cyclopropyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-7 cycloalkyl. In certain embodiments, R ² is C _3-5 cycloalkyl. In certain embodiments, R ² is cyclopropyl. [0125] As defined generally above, R ^3C is C _1-6 alkyl or hydrogen. In certain embodiments, R ^3C is C _1-6 alkyl. In certain embodiments, R ^3C is C _1-4 alkyl. In certain embodiments, R ^3C is methyl. In certain embodiments, R ^3C is hydrogen. [0126] As defined generally above, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. [0127] In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence methyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁴ is methyl. In certain embodiments, R ⁴ is hydrogen. [0128] In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 5-6 membered saturated ring having one nitrogen atom. [0129] As defined generally above, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0130] In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁵ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0131] In certain embodiments, R ⁵ represents independently for each occurrence halo. In certain embodiments, R ⁵ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁵ is methyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁵ is trifluoromethyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁵ is methoxy. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁵ is hydroxyl. In certain embodiments, R ⁵ is cyano. [0132] As defined generally above, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0133] In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁶ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0134] In certain embodiments, R ⁶ represents independently for each occurrence halo. In certain embodiments, R ⁶ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁶ is methyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁶ is trifluoromethyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁶ is methoxy. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁶ is hydroxyl. In certain embodiments, R ⁶ is cyano. [0135] As defined generally above, Ring A is ; wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² . In certain embodiments, Ring A is . In certain embodiments, Ring A is . In certain embodiments, Ring A is [0136] As defined generally above, m is 0, 1, 2, or 3. In certain embodiments, m is 0. In certain embodiments, m is 1. In certain embodiments, m is 2. In certain embodiments, m is 3. In certain embodiments, m is 0 or 1. In certain embodiments, m is 1 or 2. In certain embodiments, m is 2 or 3. In certain embodiments, m is 0, 1, or 2. In certain embodiments, m is 1, 2, or 3. [0137] As defined generally above, n is 0, 1, 2, or 3. In certain embodiments, n is 0. In certain embodiments, n is 1. In certain embodiments, n is 2. In certain embodiments, n is 3. In certain embodiments, n is 0 or 1. In certain embodiments, n is 1 or 2. In certain embodiments, n is 2 or 3. In certain embodiments, n is 0, 1, or 2. In certain embodiments, n is 1, 2, or 3. [0138] The description above describes multiple embodiments relating to compounds of Formula I-A. The patent application specifically contemplates all combinations of the embodiments. [0139] Another aspect of the invention provides a compound represented by Formula II: (II) or a pharmaceutically acceptable salt thereof; wherein: R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen; R ^1A and R ⁷ each represents independently for each occurrence halo, C _1-6 alkyl, C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl; R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ ; R ^3A and R ^3B each represents independently C _1-4 alkyl; or R ^3A is hydrogen, and R ^3B is C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring; R ^3C is C _1-6 alkyl or hydrogen; R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom; R ⁵ and R ⁶ each represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano; Ring A is ubstituted with q occur ⁷ rences of R , wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² ; m and n are each independently 0, 1, 2, or 3; and p and q are each independently 0, 1, or 2. [0140] The definitions of variables in Formula II above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition of a variable is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii). [0141] In certain embodiments, the compound is a compound of Formula II. [0142] As defined generally above, R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen. [0143] In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or C(O)N(R ⁴ ) ₂ In certain embodiments R ¹ is C16 alkyl substituted with (i) 1 2 or 3 halo and (ii) 0 or 1 occurrence of hydroxyl. In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 1 occurrence of hydroxyl. In certain embodiments, R ¹ is or In certain embodiments, R ¹ is -CH ₂ CHF ₂ . [0144] In certain embodiments, R ¹ is -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)OR ^3C . In certain embodiments, R ¹ is - C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)-(C _1-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)- (C _3-7 cycloalkyl). [0145] In certain embodiments, R ¹ is -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridinyl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridin-2-yl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is [0146] In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ In certain embodiments R ¹ is -(C _1-2 alkylene)-(6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms), wherein said heteroaryl is substituted with m occurrences of R ⁵ . [0147] In certain embodiments, R ¹ is hydrogen. In certain embodiments, R ¹ is selected from the groups depicted in the compounds in Table 4, below. [0148] As defined generally above, R ^1A represents independently for each occurrence halo, C _1-6 alkyl, C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl. In certain embodiments, R ^1A represents independently for each occurrence halo, C _1-6 alkyl, or C _1-6 haloalkyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkyl or C _1-6 haloalkyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkoxyl or hydroxyl. [0149] In certain embodiments, R ^1A represents independently for each occurrence halo. In certain embodiments, R ^1A represents independently for each occurrence fluoro or chloro. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ^1A is methyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 haloalkyl. In certain embodiments, R ^1A is trifluoromethyl. In certain embodiments, R ^1A represents independently for each occurrence C _1-6 alkoxyl. In certain embodiments, R ^1A is methoxy. In certain embodiments, R ^1A is hydroxyl. In certain embodiments, R ^1A is selected from the groups depicted in the compounds in Table 4, below. [0150] As defined generally above, R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ . [0151] In certain embodiments, R ² is phenyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is ² In certain embodiments, R is In certain embodiments, R ² is In certain embodiments, R ² is [0152] In certain embodiments, R ² is . In certain embodiments, R ² is In certain embodiments, R ² is . In certain embodiments, R ² is ² In certain embodiments, R is [0153] In certain embodiments, R ² is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridinyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridin-2-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is [0154] In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazolyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazol-5-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is . [0155] In certain embodiments, R ² is C _3-7 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-5 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is cyclopropyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-7 cycloalkyl. In certain embodiments, R ² is C _3-5 cycloalkyl. In certain embodiments, R ² is cyclopropyl. [0156] In certain embodiments, R ² is selected from the groups depicted in the compounds in Table 4, below. [0157] As defined generally above, R ^3A and R ^3B each represents independently C _1-4 alkyl; or R ^3A is hydrogen, and R ^3B is C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. [0158] In certain embodiments, R ^3A and R ^3B each represents independently C _1-4 alkyl. In certain embodiments, R ^3A and R ^3B are methyl. In certain embodiments, R ^3A is hydrogen, and R ^3B is C _1-4 alkyl. In certain embodiments, R ^3A is hydrogen, and R ^3B is methyl. In certain embodiments, R ^3A and R ^3B are taken together to represent oxo. [0159] In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-5 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a cyclopropane ring. [0160] In certain embodiments, R ^3A and R ^3B are selected from the groups depicted in the compounds in Table 4, below. [0161] As defined generally above, R ^3C is C _1-6 alkyl or hydrogen. In certain embodiments, R ^3C is C _1-6 alkyl. In certain embodiments, R ^3C is C _1-4 alkyl. In certain embodiments, R ^3C is methyl. In certain embodiments, R ^3C is hydrogen. In certain embodiments, R ^3C is selected from the groups depicted in the compounds in Table 4, below. [0162] As defined generally above, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. [0163] In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence methyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁴ is methyl. In certain embodiments, R ⁴ is hydrogen. [0164] In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 5-6 membered saturated ring having one nitrogen atom. [0165] In certain embodiments, R ⁴ is selected from the groups depicted in the compounds in Table 4, below. [0166] As defined generally above, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0167] In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁵ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0168] In certain embodiments, R ⁵ represents independently for each occurrence halo. In certain embodiments, R ⁵ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁵ is methyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁵ is trifluoromethyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁵ is methoxy. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁵ is hydroxyl. In certain embodiments, R ⁵ is cyano. [0169] In certain embodiments, R ⁵ is selected from the groups depicted in the compounds in Table 4, below. [0170] As defined generally above, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0171] In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁶ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0172] In certain embodiments, R ⁶ represents independently for each occurrence halo. In certain embodiments, R ⁶ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁶ is methyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁶ is trifluoromethyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁶ is methoxy. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁶ is hydroxyl. In certain embodiments, R ⁶ is cyano. [0173] In certain embodiments, R ⁶ is selected from the groups depicted in the compounds in Table 4, below. [0174] As defined generally above, R ⁷ represents independently for each occurrence halo, C _1-6 alkyl, C _1-6 haloalkyl, C _1-6 alkoxyl, or hydroxyl. In certain embodiments, R ⁷ represents independently for each occurrence halo, C _1-6 alkyl, or C _1-6 haloalkyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkyl or C _1-6 haloalkyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkoxyl or hydroxyl. [0175] In certain embodiments, R ⁷ represents independently for each occurrence halo. In certain embodiments, R ⁷ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁷ is methyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 haloalkyl. In certain embodiments, R ⁷ is trifluoromethyl. In certain embodiments, R ⁷ represents independently for each occurrence C _1-6 alkoxyl. In certain embodiments, R ⁷ is methoxy. In certain embodiments, R ⁷ is hydroxyl. In certain embodiments, R ⁷ is selected from the groups depicted in the compounds in Table 4, below. [0176] As defined generally above, Ring A is substituted with q occurrences of R ⁷ , wherein ψ indicates the point of attachment to the piperidine ring, and ** indicates the point of attachment to R ² . In certain embodiments, Ring A is In certain embodiments, Ring A is selected from the groups depicted in the compounds in Table 4, below. [0177] As defined generally above, m is 0, 1, 2, or 3. In certain embodiments, m is 0. In certain embodiments, m is 1. In certain embodiments, m is 2. In certain embodiments, m is 3. In certain embodiments, m is 0 or 1. In certain embodiments, m is 1 or 2. In certain embodiments, m is 2 or 3. In certain embodiments, m is 0, 1, or 2. In certain embodiments, m is 1, 2, or 3. In certain embodiments, m is selected from the values represented in the compounds in Table 4, below. [0178] As defined generally above, n is 0, 1, 2, or 3. In certain embodiments, n is 0. In certain embodiments, n is 1. In certain embodiments, n is 2. In certain embodiments, n is 3. In certain embodiments, n is 0 or 1. In certain embodiments, n is 1 or 2. In certain embodiments, n is 2 or 3. In certain embodiments, n is 0, 1, or 2. In certain embodiments, n is 1, 2, or 3. In certain embodiments, n is selected from the values represented in the compounds in Table 4, below. [0179] As defined generally above, p is 0, 1 or 2. In certain embodiments, p is 0. In certain embodiments, p is 1. In certain embodiments, p is 2. In certain embodiments, p is 0 or 1. In certain embodiments, p is 1 or 2. In certain embodiments, p is selected from the values represented in the compounds in Table 4, below. [0180] In certain embodiments, p and q are 0. [0181] As defined generally above, q is 0, 1 or 2. In certain embodiments, q is 0. In certain embodiments, q is 1. In certain embodiments, q is 2. In certain embodiments, q is 0 or 1. In certain embodiments, q is 1 or 2. In certain embodiments, q is selected from the values represented in the compounds in Table 4, below. [0182] The description above describes multiple embodiments relating to compounds of Formula II. The patent application specifically contemplates all combinations of the embodiments. [0183] Another aspect of the invention provides a compound represented by Formula TT-A:

(II -A) or a pharmaceutically acceptable salt thereof; wherein:

R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen;

R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1 , 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ ;

R ^3A and R ^3B each represents independently C _1-4 alkyl; or R ^3A is hydrogen, and R ^3B is C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring;

R ^3C is C _1-6 alkyl or hydrogen;

R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom;

R ⁵ and R ⁶ each represents independently for each occurrence halo, C _1-4 alkyl, C _1-6 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano; m and n are each independently 0, 1, 2, or 3. [0184] The definitions of variables in Formula II-A above encompass multiple chemical groups. The application contemplates embodiments where, for example, i) the definition of a variable is a single chemical group selected from those chemical groups set forth above, ii) the definition of a variable is a collection of two or more of the chemical groups selected from those set forth above, and iii) the compound is defined by a combination of variables in which the variables are defined by (i) or (ii). [0185] In certain embodiments, the compound is a compound of Formula II-A. [0186] As defined generally above, R ¹ is selected from the group consisting of: a. C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ ; b. -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl); c. -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ ; and d. hydrogen. [0187] In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl, C _1-6 alkoxyl, C _1-6 haloalkoxyl, -O-(C _3-5 cycloalkyl), oxo, -C(O)OR ^3C , or -C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 1, 2, or 3 halo, and (ii) 0 or 1 occurrence of hydroxyl. In certain embodiments, R ¹ is C _1-6 alkyl substituted with (i) 0, 1, 2, or 3 halo, and (ii) 1 occurrence of hydroxyl. In certain embodiments, R ¹ is or In certain embodiments, R ¹ is -CH ₂ CHF ₂ . [0188] In certain embodiments, R ¹ is -C(O)OR ^3C , -C(O)N(R ⁴ ) ₂ , or -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)OR ^3C . In certain embodiments, R ¹ is - C(O)N(R ⁴ ) ₂ . In certain embodiments, R ¹ is -C(O)-(C _0-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)-(C _1-4 alkylene)-(C _3-7 cycloalkyl). In certain embodiments, R ¹ is -C(O)- (C _3-7 cycloalkyl). [0189] In certain embodiments, R ¹ is -(C _0-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms, wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridinyl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is pyridin-2-yl substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is [0190] In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur), wherein said heteroaryl is substituted with m occurrences of R ⁵ . In certain embodiments, R ¹ is -(C _1-2 alkylene)-(6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms), wherein said heteroaryl is substituted with m occurrences of R ⁵ . [0191] In certain embodiments, R ¹ is hydrogen. [0192] As defined generally above, R ² is phenyl; a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or C _3-7 cycloalkyl; each of which is substituted with n occurrences of R ⁶ . [0193] In certain embodiments, R ² is phenyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is ² , , . In certain embodiments, R is In certain embodiments, R ² is In certain embodiments, R ² is [0194] In certain embodiments, R ² is . In certain embodiments, R ² is . In certain embodiments, R ² is . In certain embodiments, R ² is ² In certain embodiments, R is [0195] In certain embodiments, R ² is a 5-6 membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 5-membered monocyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 6-membered monocyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridinyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is pyridin-2-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is [0196] In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is an 8-10 membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is a 9-membered bicyclic heteroaryl having 1 or 2 nitrogen atoms; wherein said heteroaryl is substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazolyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is indazol-5-yl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is [0197] In certain embodiments, R ² is C _3-7 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-5 cycloalkyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is cyclopropyl substituted with n occurrences of R ⁶ . In certain embodiments, R ² is C _3-7 cycloalkyl. In certain embodiments, R ² is C _3-5 cycloalkyl. In certain embodiments, R ² is cyclopropyl. [0198] As defined generally above, R ^3A and R ^3B each represents independently C _1-4 alkyl; or R ^3A is hydrogen, and R ^3B is C _1-4 alkyl; or R ^3A and R ^3B are taken together to represent oxo; or R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. [0199] In certain embodiments, R ^3A and R ^3B each represents independently C _1-4 alkyl. In certain embodiments, R ^3A and R ^3B are methyl. In certain embodiments, R ^3A is hydrogen, and R ^3B is C _1-4 alkyl. In certain embodiments, R ^3A is hydrogen, and R ^3B is methyl. In certain embodiments, R ^3A and R ^3B are taken together to represent oxo. [0200] In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-7 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a 3-5 membered saturated carbocyclic ring. In certain embodiments, R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a cyclopropane ring. [0201] As defined generally above, R ^3C is C _1-6 alkyl or hydrogen. In certain embodiments, R ^3C is C _1-6 alkyl. In certain embodiments, R ^3C is C _1-4 alkyl. In certain embodiments, R ^3C is methyl. In certain embodiments, R ^3C is hydrogen. [0202] As defined generally above, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen, or two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. [0203] In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence methyl or hydrogen. In certain embodiments, R ⁴ represents independently for each occurrence C _1-6 alkyl. In certain embodiments, R ⁴ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁴ is methyl. In certain embodiments, R ⁴ is hydrogen. [0204] In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 4-7 membered saturated ring having one nitrogen atom. In certain embodiments, two occurrences of R ⁴ attached to the same nitrogen atom are taken together with said nitrogen atom to form a 5-6 membered saturated ring having one nitrogen atom. [0205] As defined generally above, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0206] In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁵ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0207] In certain embodiments, R ⁵ represents independently for each occurrence halo. In certain embodiments, R ⁵ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁵ is methyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁵ is trifluoromethyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁵ is methoxy. In certain embodiments, R ⁵ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁵ is hydroxyl. In certain embodiments, R ⁵ is cyano. [0208] As defined generally above, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, C _3-7 cycloalkyl, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. [0209] In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, or C _1-4 alkoxyl. In certain embodiments, R ⁶ represents independently for each occurrence fluoro, chloro, methyl, trifluoromethyl, or methoxy. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl, C _1-4 haloalkyl, C _1-4 hydroxyalkyl, or C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence halo, C _1-4 alkoxyl, C _1-4 haloalkoxyl, hydroxyl, or cyano. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl, C _1-4 haloalkoxyl, or hydroxyl. [0210] In certain embodiments, R ⁶ represents independently for each occurrence halo. In certain embodiments, R ⁶ represents independently for each occurrence fluoro or chloro. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkyl. In certain embodiments, R ⁶ is methyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkyl. In certain embodiments, R ⁶ is trifluoromethyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 hydroxyalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _3-7 cycloalkyl. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 alkoxyl. In certain embodiments, R ⁶ is methoxy. In certain embodiments, R ⁶ represents independently for each occurrence C _1-4 haloalkoxyl. In certain embodiments, R ⁶ is hydroxyl. In certain embodiments, R ⁶ is cyano. [0211] As defined generally above, m is 0, 1, 2, or 3. In certain embodiments, m is 0. In certain embodiments, m is 1. In certain embodiments, m is 2. In certain embodiments, m is 3. In certain embodiments, m is 0 or 1. In certain embodiments, m is 1 or 2. In certain embodiments, m is 2 or 3. In certain embodiments, m is 0, 1, or 2. In certain embodiments, m is 1, 2, or 3. [0212] As defined generally above, n is 0, 1, 2, or 3. In certain embodiments, n is 0. In certain embodiments, n is 1. In certain embodiments, n is 2. In certain embodiments, n is 3. In certain embodiments, n is 0 or 1. In certain embodiments, n is 1 or 2. In certain embodiments, n is 2 or 3. In certain embodiments, n is 0, 1, or 2. In certain embodiments, n is 1, 2, or 3. [0213] The description above describes multiple embodiments relating to compounds of Formula II-A. The patent application specifically contemplates all combinations of the embodiments. [0214] Another aspect of the invention provides a compound in Table 1, 2, 3, or 4 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 1, 2, 3, or 4 below. In certain embodiments, the compound is a compound in Table 1, 2, or 3 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 1, 2, or 3 below. In certain embodiments, the compound is a compound in Table 2 or 3 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 2 or 3 below. [0215] In certain embodiments, the compound is a compound in Table 1 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 1 below. In certain embodiments, the compound is a compound in Table 2 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 2 below. In certain embodiments, the compound is a compound in Table 3 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 3 below. In certain embodiments, the compound is a compound in Table 4 below, or a pharmaceutically acceptable salt thereof. In certain embodiments, the compound is a compound in Table 4 below. TABLE 1.

TABLE 2. TABLE 3. TABLE 4. [0216] Methods for preparing compounds described herein are illustrated in the following synthetic Scheme. The Scheme is given for the purpose of illustrating the invention, and is not intended to limit the scope or spirit of the invention. Starting materials shown in the Scheme can be obtained from commercial sources or can be prepared based on procedures described in the literature. Additional strategies for preparing starting materials and other piperidinyl- methylpurine pyrimidines and related compounds are described in, for example, WO 2021/028854, the entirety of which is hereby incorporated by reference. [0217] In the Scheme, it is understood by one skilled in the art of organic synthesis that the functionality present on various portions of the molecule should be compatible with the reagents and reactions proposed. Substituents not compatible with the reaction conditions will be apparent to one skilled in the art, and alternate methods are therefore indicated (for example, use of protecting groups or alternative reactions). Protecting group chemistry and strategy is well known in the art, for example, as described in detail in “Protecting Groups in Organic Synthesis”, T. W. Greene and P. G. M. Wuts, 3 ^rd edition, John Wiley & Sons, 1999, the entire contents of which are hereby incorporated by reference. [0218] The synthetic route illustrated in Scheme 1 is a general method for preparing piperidinyl-methylpurine benzenes and related compounds G. Transition-metal-mediated coupling of R ² -M (wherein M is an appropriate metal, such as a boronic acid, boronate ester, organotin, or zinc reagent) with benzene or pyridine A (wherein LG ¹ is a leaving group, such as bromide, iodide, or a sulfonate; LG ² is a leaving group, such as fluoride, chloride, or a sulfonate; and R is an appropriate group, such as methyl, ethyl, or benzyl) affords R ² -substituted benzene or pyridine B. Condensation of piperidine C (wherein PG ¹ is a protecting group, such as benzyl) with benzene or pyridine B (using, for example, nucleophilic aromatic substitution conditions with a base, such as K ₂ CO ₃ or DIPEA, in a polar aprotic solvent, such as DMSO) affords piperidine D. Addition of the R ^3A and R ^3B substituents to piperidine D, as described in more detail below, affords alcohol E (or carboxylic acid E, when R ^3A and R ^3B are taken together to represent oxo). Activation of the hydroxyl group of compound E, either in a discrete step (for example, to a sulfonate, using, for example, tosyl chloride and a base, such as DIPEA) or in situ (for example, under Mitsunobu conditions, or amide coupling conditions, when R ^3A and R ^3B are taken together to represent oxo), and displacement with protected adenine F (wherein PG ² is a protecting group, such as Boc), followed by global deprotection (using, for example, reduction, such as hydrogenolysis, when at least one of PG ¹ and/or PG ² is benzyl, and/or acidic conditions, such as TFA or HC1, when at least one of PG ¹ and/or PG ² is Boc), affords piperidinyl-methylpurine benzenes and related compounds G. SCHEME 1. [0219] Addition of the R ^3A and R ^3B substituents to piperidine D to afford alcohol E, proceeds under appropriate conditions for the desired functionality. For example, reduction (using, for example, a metal hydride, such as LiA1H ₄ ) affords alcohol E where R ^3A and R ^3B are hydrogen. Alternatively, conversion of the ester of piperidine D to the aldehyde (for example, via direct partial reduction, using, for example, a metal hydride, such as DIBAL-H; or via reduction to the alcohol as described previously, followed by oxidation, using, for example, Dess-Martin periodinane), followed by addition of an alkyl-metal reagent, such as a Grignard or alkyl lithium, affords alcohol E where R ^3A is hydrogen and R ^3B is an alkyl group. Oxidation of the resulting alcohol (using, for example, Dess-Martin periodinane), followed by addition of an alkyl-metal reagent, such as a Grignard or alkyl lithium, affords alcohol E where R ^3A and R ^3B are both alkyl groups. Alternatively, cyclopropanation of the ester of piperidine D (using, for example, titanium isopropoxide and ethyl Grignard) affords alcohol E where R ^3A and R ^3B are taken together with the carbon atom to which they are attached to form a cyclopropyl ring. Alternatively, saponification of the ester of piperidine D (using, for example, a hydroxide base, such as lithium hydroxide) affords carboxylic acid E (where R ^3A and R ^3B are taken together to represent oxo). [0220] The modular synthetic route illustrated in Scheme 1 can be readily modified by one of skill in the art to alter the order of introducing the R ² , piperidine, R ^3A , and R ^3B substituents, given the orthogonal functional groups present in benzene or pyridine A. For example, cross-coupling addition of R ² to form compound B can be followed by addition of R ^3A , R ^3B , and adenine, and the synthesis of piperidinyl-methylpurine benzenes and related compounds G concluded with condensation with piperidine C and global deprotection. Alternatively, piperidine C can first be condensed with benzene or pyridine A, followed by addition of R ^3A , R ^3B , and adenine, and the synthesis of piperidinyl-methylpurine benzenes and related compounds G concluded with cross- coupling addition of R ² and global deprotection. [0221] The modular synthetic route illustrated in Scheme 1 can also be readily modified by one of skill in the art to provide additional piperidinyl-methylpurine benzenes and related compounds by conducting functional group transformations on the intermediate and final compounds. Such functional group transformations are well known in the art, as described in, for example, “Comprehensive Organic Synthesis” (B.M. Trost & I. Fleming, eds., 1991-1992). II. Therapeutic Applications of Piperidinyl-Methylpurine Benzenes and Related Compounds [0222] The piperidinyl-methylpurine benzenes and related compounds described herein, such as a compound of Formula I, I-A, II, or II-A, or other compounds in Section I, provide therapeutic benefits to subjects suffering from cancer and other diseases or conditions. Accordingly, one aspect of the invention provides a method for treating a disease or condition mediated by nuclear SET domain-containing protein 2 (NSD2). The method comprises administering a therapeutically effective amount of a compound described herein, such as a compound of Formula I, I-A, II, or II- A, to a subject in need thereof to treat the disease or condition. In certain embodiments, the compound is a compound of Formula I, I-A, II, or II-A defined by one of the embodiments described above. [0223] Examples of diseases or conditions that are mediated by NSD2 include but is not limited to breast cancer, cervical cancer, skin cancer (particularly skin squamous cell carcinoma), ovarian cancer, gastric cancer, prostate cancer, pancreatic cancer, lung cancer, hepatocellular carcinoma, head and neck cancer, peripheral nerve sheath tumor, osteosarcoma, multiple myeloma, neuroblastoma, leukemia (particularly acute lymphoblastic leukemia), non-Hodgkin’s lymphoma (particularly mantle cell lymphoma), and pulmonary arterial hypertension. [0224] In certain embodiments, said disease or condition mediated by NSD2 is cancer. [0225] In certain embodiments, said disease or condition mediated by NSD2 is selected from a solid tumor, leukemia, myeloma, lymphoma, and hypertension. In certain embodiments, said disease or condition mediated by NSD2 is a solid tumor. In certain embodiments, said disease or condition mediated by NSD2 is selected from leukemia, myeloma, and lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is leukemia. In certain embodiments, said disease or condition mediated by NSD2 is myeloma. In certain embodiments, said disease or condition mediated by NSD2 is lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is hypertension. [0226] In certain embodiments, said disease or condition mediated by NSD2 is breast cancer, cervical cancer, skin cancer, ovarian cancer, gastric cancer, prostate cancer, pancreatic cancer, lung cancer, hepatocellular carcinoma, head and neck cancer, peripheral nerve sheath tumor, osteosarcoma, multiple myeloma, neuroblastoma, leukemia, non-Hodgkin’s lymphoma, or pulmonary arterial hypertension. In certain embodiments, said disease or condition mediated by NSD2 is breast cancer. In certain embodiments, said disease or condition mediated by NSD2 is cervical cancer. In certain embodiments, said disease or condition mediated by NSD2 is ovarian cancer. In certain embodiments, said disease or condition mediated by NSD2 is gastric cancer. In certain embodiments, said disease or condition mediated by NSD2 is prostate cancer. In certain embodiments, said disease or condition mediated by NSD2 is pancreatic cancer. In certain embodiments, said disease or condition mediated by NSD2 is hepatocellular carcinoma. In certain embodiments, said disease or condition mediated by NSD2 is head and neck cancer. In certain embodiments, said disease or condition mediated by NSD2 is a peripheral nerve sheath tumor. In certain embodiments, said disease or condition mediated by NSD2 is osteosarcoma. In certain embodiments, said disease or condition mediated by NSD2 is multiple myeloma. In certain embodiments, said disease or condition mediated by NSD2 is neuroblastoma. In certain embodiments, said disease or condition mediated by NSD2 is pulmonary arterial hypertension. [0227] In certain embodiments, said disease or condition mediated by NSD2 is acute lymphoblastic leukaemia, skin squamous cell carcinoma, or mantle cell lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is acute lymphoblastic leukaemia. In certain embodiments, said disease or condition mediated by NSD2 is skin squamous cell carcinoma. In certain embodiments, said disease or condition mediated by NSD2 is mantle cell lymphoma. [0228] In certain embodiments, said disease or condition mediated by NSD2 is lung cancer. In certain embodiments, said disease or condition mediated by NSD2 is small cell or non-small cell lung cancer. In certain embodiments, said disease or condition mediated by NSD2 is small cell lung cancer. In certain embodiments, said disease or condition mediated by NSD2 is non-small cell lung cancer. [0229] In certain embodiments, said disease or condition mediated by NSD2 is leukemia. In certain embodiments, said disease or condition mediated by NSD2 is acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), or chronic myelomonocytic leukemia (CMML). In certain embodiments, said disease or condition mediated by NSD2 is AML. In certain embodiments, said disease or condition mediated by NSD2 is CML. In certain embodiments, said disease or condition mediated by NSD2 is CMML. [0230] In certain embodiments, said disease or condition mediated by NSD2 is skin cancer. In certain embodiments, said disease or condition mediated by NSD2 is melanoma, basal cell carcinoma, or squamous cell carcinoma. In certain embodiments, said disease or condition mediated by NSD2 is melanoma. In certain embodiments, said disease or condition mediated by NSD2 is basal cell carcinoma. [0231] In certain embodiments, said disease or condition mediated by NSD2 is lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is Hodgkin’s lymphoma or non- Hodgkin’s lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is Hodgkin’s lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is non-Hodgkin’s lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is mantle cell lymphoma or diffuse large B cell lymphoma. In certain embodiments, said disease or condition mediated by NSD2 is diffuse large B cell lymphoma. [0232] In certain embodiments, said disease or condition mediated by NSD2 is myeloma. [0233] In certain embodiments, said disease or condition mediated by NSD2 is thyroid cancer. In certain embodiments, said disease or condition mediated by NSD2 is colon cancer. [0234] In certain embodiments, the cancer overexpresses NSD2. In certain embodiments, the cancer has a mutation in NSD2. In certain embodiments, the cancer has an activating mutation in NSD2. In certain embodiments, the cancer has the t(4;14)(p16.3;q32.3) translocation in NSD2. In certain embodiments, the cancer has an E1099K mutation in NSD2. In certain embodiments, the cancer has an T1150A mutation in NSD2. [0235] In certain embodiments, the subject is a human. In certain embodiments, the subject is an adult human. In certain embodiments, the subject is a pediatric human. In certain embodiments, the subject is a geriatric human. [0236] Another aspect of the invention provides for the use of a compound described herein (such as a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) in the manufacture of a medicament. In certain embodiments, the medicament is for treating a disease or condition described herein, such as cancer. [0237] Another aspect of the invention provides for the use of a compound described herein (such as a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) for treating a disease or condition, such as a disease or condition described herein (for example, cancer). [0238] Further, compounds described herein, such as a compound of Formula I, I-A, II, or II-A, or other compounds in Section I, inhibit the activity of nuclear SET domain-containing protein 2 (NSD2). Accordingly, another aspect of the invention provides a method of inhibiting the activity of nuclear SET domain-containing protein 2 (NSD2). The method comprises contacting a NSD2 with an effective amount of a piperidinyl-methylpurine benzene or related compound described herein, such as a compound of Formula I, I-A, II, or II-A, or other compounds in Section I, to inhibit the activity of said NSD2. In certain embodiments, the compound is a compound of Formula I, I-A, II, or II-A defined by one of the embodiments described above. [0239] Compounds may be tested for ability to bind to and/or inhibit NSD2 activity according to any of various assays known in the art, including, for example, LC-MS/MS enzymatic assays monitoring SAH production, cellular FRET assays, cellular ELISA assays, methyltransferase enzymatic luminescence assays monitoring SAH production, and radiometric assays using tritium- labeled SAM. Such assays are described in, for example, WO 2021/028854 and Coussens, N. P. et al. J. Biol. Chem. (2018) Vol. 293, No.35, pp.13750-13755; the entirety of each of which is hereby incorporated by reference. III. Combination Therapy

[0240] Another aspect of the invention provides for combination therapy. Piperidinyl- methylpurine benzene or related compounds described herein (e.g., a compound of Formula I, I- A, II, II-A , or other compounds in Section I) or their pharmaceutically acceptable salts may be used in combination with additional therapeutic agents to treat diseases or conditions, such as a cancer.

[0241] Accordingly, in some embodiments, the present invention provides a method of treating a disclosed disease or condition comprising administering to a patient in need thereof an effective amount of a compound disclosed herein and co-administering simultaneously or sequentially an effective amount of one or more additional therapeutic agents, such as those described herein. In some embodiments, the method includes co-administering one additional therapeutic agent. In some embodiments, the method includes co-administering two additional therapeutic agents.

[0242] One or more other therapeutic agents may be administered separately from a compound or composition of the invention, as part of a multiple dosage regimen. Alternatively, one or more other therapeutic agents may be part of a single dosage form, mixed together with a compound of this invention in a single composition. If administered as a multiple dosage regime, one or more other therapeutic agent and a compound or composition of the invention may be administered simultaneously, sequentially or within a period of time from one another.

[0243] In certain embodiments, the additional therapeutic agent is an anti-cancer agent, anti- allergic agent, anti-nausea agent (or anti-emetic), pain reliever, cytoprotective agent, or a combination thereof. In certain embodiments, the additional therapeutic agent is an anti-cancer agent, an analgesic, an anti-inflammatory agent, or a combination thereof.

[0244] In certain embodiments, the additional therapeutic agent is an anti-cancer agent or chemo-therapeutic agent. Examples of anti-cancer agents considered for use in combination therapies of the invention include but are not limited erlotinib, bortezomib, fulvestrant, sunitib, imatinib mesylate, letrozole, finasunate, platins such as oxaliplatin, carboplatin, and cisplatin, fmasunate, fluorouracil, rapamycin, leucovorin, lapatinib, lonafamib, sorafenib, gefitinib, camptothecin, topotecan, bryostatin, adezelesin, anthracyclin, carzelesin, bizelesin, dolastatin, auristatins, duocarmycin, eleutherobin, taxols such as paclitaxel or docetaxel, cyclophosphamide, doxorubicin, vincristine, prednisone or prednisolone, other alkylating agents such as mechlorethamine, chlorambucil, and ifosfamide, antimetabolites such as azathioprine or mercaptopurine, other microtubule inhibitors (vinca alkaloids like vincristine, vinblastine, vinorelbine, and vindesine, as well as taxanes), podophyllotoxins (etoposide, teniposide, etoposide phosphate, and epipodophyllotoxins), topoisomerase inhibitors, other cytotoxins such as actinomycin, daunorubicin, valrubicin, idarubicin, edrecolomab, epirubicin, bleomycin, plicamycin, mitomycin, as well as other anticancer antibodies (cetuximab, bevacizumab, ibritumomab, abagovomab, adecatumumab, afutuzumab, alacizumab, alemtuzumab, anatumomab, apolizumab, bavituximab, belimumab, bivatuzumab mertansine, blinatumomab, brentuximab vedotin, cantuzumab mertansine, catumazomab, cetuximab, citatuzumab bogatox, cixutumumab, clivatuzumab tetraxetan, conatumumab, dacetuzumab, daclizumab, detumomab, ecromeximab, edrecolomab, elotuzumab, epratuzumab, ertumaxomab, etaracizumab, farletuzumab, figitumumab, fresolimumab, galiximab, gembatumumab vedotin, gemtuzumab, ibritumomab tiuxetan, inotuzumab ozogamicin, intetumumab, ipilimumab, iratumumab, labetuzumab, lexatumumab, lintuzumab, lucatumumab, lumilisimab, mapatumumab, matuzumab, milatuzumab, mitumomab, nacolomab tafenatox, naptumomab estafenatox, necitumumab, nimotuzumab, ofatumumab, olaratumab, oportuzumab monatox, oregovomab, panitumumab, pemtumomab, pertuzumab, pintumomab, pritumumab, ramucirumab, rilotumumab, robatumumab, rituximab, sibrotuzumab, tacatuzumab tetraxetan, taplitumomab paptox, tenatumomab, ticilimumab, tigatuzumab, tositumomab or ¹³¹ I-tositumomab, trastuzumab, tremelimumab, tuocotuzumab celmoleukin, veltuzumab, visilizumab, volocixumab, votumumab, zalutumumab, zanolimumab, IGN-101, MDX-010, ABX-EGR, EMD72000, ior-t1, MDX-220, MRA, H-11 scFv, huJ591, TriGem, TriAb, R3, MT-201, G-250, ACA-125, Onyvax-105, CD:- 960,Cea-Vac, BrevaRex AR54, IMC-1C11, GlioMab-H, ING-1, anti-LCG MAbs, MT-103, KSB- 303, Therex, KW2871, anti-HMI.24, Anti-PTHrP, 2C4 antibody, SGN-30, TRAIL-RI MAb, Prostate Cancer antibody, H22xKi-r, ABX-Mai, Imuteran, Monopharm-C), and antibody-drug conjugates comprising any of the above agents (especially auristatins MMAE and MMAF, maytansinoids like DM-1, calicheamycins, or various cytotoxins). [0245] In certain embodiments, the additional therapeutic agent is selected from anastrozole (ARIMIDEX®), bicalutamide (CASODEX®), bleomycin sulfate (BLENOXANE®), busulfan (MYLERAN®), busulfan injection (BUSULFEX®), capecitabine (XELODA®), N4- pentoxycarbonyl 5 deoxy 5 fluorocytidine carboplatin (PARAPLATIN®) carmustine (BiCNU®), chlorambucil (LEUKERAN®), cisplatin (PLATINOL®), cladribine (LEUSTATIN®), cyclophosphamide (CYTOXAN® or NEOSAR®), cytarabine, cytosine arabinoside (CYTOSAR-U®), cytarabine liposome injection (DEPOCYT®), dacarbazine (DTIC- Dome®), dactinomycin (actinomycin D, COSMEGAN®), daunorubicin hydrochloride (CERUBIDINE®), daunorubicin citrate liposome injection (DAUNOXOME®), dexamethasone, docetaxel (TAXOTERE®), doxorubicin hydrochloride (ADRIAMYCIN®, RUBEX®), etoposide (VEPESID®), fludarabine phosphate (FLUDARA®), 5-fluorouracil (ADRUCIL®, EFUDEX®), flutamide (EULEXIN®), tezacitibine, gemcitabine (difluorodeoxycitidine), hydroxyurea (HYDREA®), idarubicin (IDAMYCIN®), ifosfamide (IFEX®), irinotecan (CAMPTOSAR®), L- asparaginase (ELSPAR®), leucovorin calcium, melphalan (ALKERAN®), 6-mercaptopurine (PURINETHOL®), methotrexate (FOLEX®), mitoxantrone (NOVANTRONE®), gemtuzumab ozogamicin (MYLOTARGTM), paclitaxel (TAXOL®), nab-paclitaxel (ABRAXANE®), phoenix (Yttrium90/MX-DTPA), pentostatin, polifeprosan 20 with carmustine implant (GLIADEL®), tamoxifen citrate (NOLVADEX®), teniposide (VUMON®), 6-thioguanine, thiotepa, tirapazamine (TIRAZONE®), topotecan hydrochloride for injection (HYCAMPTIN®), vinblastine (VELBAN®), vincristine (ONCOVIN®), and vinorelbine (NAVELBINE®). [0246] In certain embodiments, the additional therapeutic agent is capable of inhibiting BRAF, MEK, CDK4/6, SHP-2, HDAC, EGFR, MET, mTOR, PI3K or AKT, or a combination thereof. In a particular embodiment, the compounds of the present invention are combined with another therapeutic agent selected from vemurafinib, debrafinib, LGX818, trametinib, MEK162, LEE011, PD-0332991, panobinostat, verinostat, romidepsin, cetuximab, gefitinib, erlotinib, lapatinib, panitumumab, vandetanib, INC280, everolimus, simolimus, BMK120, BYL719 or CLR457, or a combination thereof. [0247] In certain embodiments, the additional therapeutic agent is selected based on the disease or condition that is being treated. For example, in the treatment of melanoma, the additional therapeutic agent is selected from aldesleukin (e.g., PROLEUKIN®), dabrafenib (e.g., TAFINLAR®), dacarbazine, recombinant interferon alfa-2b (e.g., INTRON® A), ipilimumab, trametinib (e.g., MEKINIST®), peginterferon alfa-2b (e.g., PEGINTRON®, SYLATRONTM), vemurafenib (e.g., ZELBORAF®)), and ipilimumab (e.g., YERVOY®). [0248] For the treatment of ovarian cancer, the additional therapeutic agent is selected from doxorubicin hydrochloride (Adriamycin®), carboplatin (PARAPLATIN®), cyclophosphamide (CYTOXAN®, NEOSAR®), cisplatin (PLATINOL®, PLATINOL-AQ®), doxorubicin hydrochloride liposome (DOXIL®, DOX-SL®, EVACET®, LIPODOX®), gemcitabine hydrochloride (GEMZAR®), topotecan hydrochloride (HYCAMTIN®), and paclitaxel (TAXOL®). [0249] For the treatment of thyroid cancer, the additional therapeutic agent is selected from doxorubicin hydrochloride (Adriamycin®), cabozantinib-S-malate (COMETRIQ®), and vandetanib (CAPRELSA®). [0250] For the treatment of colon cancer, the additional therapeutic agent is selected from fluorouracil (e.g., ADRUCIL®, EFUDEX®, FLUOROPLEX®), bevacizumab (AVASTIN®), irinotecan hydrochloride (CAMPTOSTAR®), capecitabine (XELODA®), cetuximab (ERBITUX®), oxaliplatin (ELOXATIN®), leucovorin calcium (WELLCOVORIN®), regorafenib (STIVARGA®), panitumumab (VECTIBIX®), and ziv-aflibercept (ZALTRAP®). [0251] For the treatment of lung cancer, the additional therapeutic agent is selected from methotrexate, methotrexate LPF (e.g., FOLEX®, FOLEX PFS®, Abitrexate®, MEXATE®, MEXATE-AQ®), paclitaxel (TAXOL®), paclitaxel albumin-stabilized nanoparticle formulation (ABRAXANE®), afatinib dimaleate (GILOTRIF®), pemetrexed disodium (ALIMTA®), bevacizumab (AVASTIN®), carboplatin (PARAPLATIN®), cisplatin (PLATINOL®, PLATINOL-AQ®), crizotinib (XALKORI®), erlotinib hydrochloride (TARCEVA®), gefitinib (IRESSA®), and gemcitabine hydrochloride (GEMZAR®). [0252] For the treatment of pancreatic cancer, the other therapeutic agent may be selected from fluorouracil (ADRUCIL®), EFUDEX®, FLUOROPLEX®), erlotinib hydrochloride (TARCEVA®), gemcitabine hydrochloride (GEMZAR®), and mitomycin or mitomycin C (MITOZYTREXTM, MUTAMYCIN®). [0253] For the treatment of cervical cancer, the additional therapeutic agent is selected from bleomycin (BLENOXANE®), cisplatin (PLATINOL®, PLATINOL-AQ®) and topotecan hydrochloride (HYCAMTIN®). [0254] For the treatment of head and neck cancer, the additional therapeutic agent is selected from methotrexate, methotrexate LPF (e.g., FOLEX®, FOLEX PFS®, Abitrexate®, MEXATE®, MEXATE-AQ®), fluorouracil (ADRUCIL®, EFUDEX®, FLUOROPLEX®), bleomycin (BLENOXANE®), cetuximab (ERBITUX®), cisplatin (PLATINOL®, PLATINOL-AQ®) and docetaxel (TAXOTERE®). [0255] For the treatment of leukemia, including chronic myelomonocytic leukemia (CMML), the additional therapeutic agent is selected from bosutinib (BOSULIF®), cyclophosphamide (CYTOXAN®, NEOSAR®), cytarabine (CYTOSAR-U®, TARABINE PFS®), dasatinib (SPRYCEL®), imatinib mesylate (GLEEVEC®), ponatinib (ICLUSIG®), nilotinib (TASIGNA®) and omacetaxine mepesuccinate (SYNRIBO®). [0256] In some instances, patients may experience allergic reactions to the compounds of the present invention and/or other anti-cancer agent(s) during or after administration. Therefore, anti- allergic agents may be administered to minimize the risk of an allergic reaction. Suitable anti- allergic agents include corticosteroids, such as dexamethasone (e.g., DECADRON®), beclomethasone (e.g., BECLOVENT®), hydrocortisone (also known as cortisone, hydrocortisone sodium succinate, hydrocortisone sodium phosphate; e.g., ALA-CORT®, hydrocortisone phosphate, Solu-CORTEF®, HYDROCORT Acetate® and LANACORT®), prednisolone (e.g., DELTA-Cortel®, ORAPRED®, PEDIAPRED® and PRELONE®), prednisone (e.g., DELTASONE®, LIQUID RED®, METICORTEN® and ORASONE®), methylprednisolone (also known as 6-methylprednisolone, methylprednisolone acetate, methylprednisolone sodium succinate; e.g., DURALONE®, MEDRALONE®, MEDROL®, M-PREDNISOL® and SOLU- MEDROL®); antihistamines, such as diphenhydramine (e.g., BENADRYL®), hydroxyzine, and cyproheptadine; and bronchodilators, such as the beta-adrenergic receptor agonists, albuterol (e.g., PROVENTIL®), and terbutaline (BRETHINE®). [0257] In other instances, patients may experience nausea during and after administration of the compound of the present invention and/or other anti-cancer agent(s). Therefore, anti-emetics may be administered in preventing nausea (upper stomach) and vomiting. Suitable anti-emetics include aprepitant (EMEND®), ondansetron (ZOFRAN®), granisetron HCl (KYTRIL®), lorazepam (ATIVAN®. dexamethasone (DECADRON®), prochlorperazine (COMPAZINE®), casopitant (REZONIC® and Zunrisa®), and combinations thereof. [0258] In yet other instances, medication to alleviate the pain experienced during the treatment period is prescribed to make the patient more comfortable. Common over-the-counter analgesics, such TYLENOL®, are often used. Opioid analgesic drugs such as hydrocodone/paracetamol or hydrocodone/acetaminophen (e.g., VICODIN®), morphine (e.g., ASTRAMORPH® or AVINZA®), oxycodone (e.g., OXYCONTIN® or PERCOCET®), oxymorphone hydrochloride (OPANA®), and fentanyl (e.g., DURAGESIC®) are also useful for moderate or severe pain. [0259] Furthermore, cytoprotective agents (such as neuroprotectants, free-radical scavengers, cardioprotectors, anthracycline extravasation neutralizers, nutrients and the like) may be used as an adjunct therapy to protect normal cells from treatment toxicity and to limit organ toxicities. Suitable cytoprotective agents include amifostine (ETHYOL®), glutamine, dimesna (TAVOCEPT®), mesna (MESNEX®), dexrazoxane (ZINECARD® or TOTECT®), xaliproden (XAPRILA®), and leucovorin (also known as calcium leucovorin, citrovorum factor and folinic acid). [0260] In yet another aspect, a compound of the present invention may be used in combination with known therapeutic processes, for example, with the administration of hormones or in radiation therapy. In certain instances, a compound of the present invention may be used as a radiosensitizer, especially for the treatment of tumors which exhibit poor sensitivity to radiotherapy. [0261] The doses and dosage regimen of the active ingredients used in the combination therapy may be determined by an attending clinician. In certain embodiments, the compound described herein (e.g., a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) and the additional therapeutic agent(s) are administered in doses commonly employed when such agents are used as monotherapy for treating the disease or condition. In other embodiments, the compound described herein (e.g., a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) and the additional therapeutic agent(s) are administered in doses lower than the doses commonly employed when such agents are used as monotherapy for treating the disease or condition. In certain embodiments, the compound described herein (e.g., a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) and the additional therapeutic agent(s) are present in the same composition, which is suitable for oral administration. [0262] In certain embodiments, the compound described herein (e.g., a compound of Formula I, I-A, II, or II-A, or other compounds in Section I) and the additional therapeutic agent(s) may act additively or synergistically. A synergistic combination may allow the use of lower dosages of one or more agents and/or less frequent administration of one or more agents of a combination therapy. A lower dosage or less frequent administration of one or more agents may lower toxicity of the therapy without reducing the efficacy of the therapy. [0263] Another aspect of this invention is a kit comprising a therapeutically effective amount of a compound described herein (e.g., a compound of Formula I, I-A, II, or II-A, or other compounds in Section I), a pharmaceutically acceptable carrier, vehicle or diluent, and optionally at least one additional therapeutic agent listed above. In certain embodiments, the kit further comprises instructions, such as instructions for treating a disease described herein. IV. Pharmaceutical Compositions and Dosing Considerations [0264] As indicated above, the invention provides pharmaceutical compositions, which comprise a therapeutically-effective amount of one or more of the compounds described above, formulated together with one or more pharmaceutically acceptable carriers (additives) and/or diluents. The pharmaceutical compositions may be specially formulated for administration in solid or liquid form, including those adapted for the following: (1) oral administration, for example, drenches (aqueous or non-aqueous solutions or suspensions), tablets, e.g., those targeted for buccal, sublingual, and systemic absorption, boluses, powders, granules, pastes for application to the tongue; (2) parenteral administration, for example, by subcutaneous, intramuscular, intravenous or epidural injection as, for example, a sterile solution or suspension, or sustained-release formulation; (3) topical application, for example, as a cream, ointment, or a controlled-release patch or spray applied to the skin; (4) intravaginally or intrarectally, for example, as a pessary, cream or foam; (5) sublingually; (6) ocularly; (7) transdermally; or (8) nasally. In certain embodiments, the invention provides a pharmaceutical composition comprising a compound described herein (e.g., a compound of Formula I, I-A, II, or II-A) and a pharmaceutically acceptable carrier. [0265] The phrase “therapeutically effective amount” as used herein means that amount of a compound, material, or composition comprising a compound of the present invention which is effective for producing some desired therapeutic effect in at least a sub-population of cells in an animal at a reasonable benefit/risk ratio applicable to any medical treatment. [0266] The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. [0267] Wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the compositions. [0268] Examples of pharmaceutically-acceptable antioxidants include: (1) water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like; (2) oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha- tocopherol, and the like; and (3) metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like. [0269] Formulations of the present invention include those suitable for oral, nasal, topical (including buccal and sublingual), rectal, vaginal and/or parenteral administration. The formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will vary depending upon the host being treated, the particular mode of administration. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound which produces a therapeutic effect. Generally, out of one hundred percent, this amount will range from about 0.1 percent to about ninety-nine percent of active ingredient, preferably from about 5 percent to about 70 percent, most preferably from about 10 percent to about 30 percent. [0270] In certain embodiments, a formulation of the present invention comprises an excipient selected from the group consisting of cyclodextrins, celluloses, liposomes, micelle forming agents, e.g., bile acids, and polymeric carriers, e.g., polyesters and polyanhydrides; and a compound of the present invention. In certain embodiments, an aforementioned formulation renders orally bioavailable a compound of the present invention. [0271] Methods of preparing these formulations or compositions include the step of bringing into association a compound of the present invention with the carrier and, optionally, one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association a compound of the present invention with liquid carriers, or finely divided solid carriers, or both, and then, if necessary, shaping the product. [0272] Formulations of the invention suitable for oral administration may be in the form of capsules, cachets, pills, tablets, lozenges (using a flavored basis, usually sucrose and acacia or tragacanth), powders, granules, or as a solution or a suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as an elixir or syrup, or as pastilles (using an inert base, such as gelatin and glycerin, or sucrose and acacia) and/or as mouth washes and the like, each containing a predetermined amount of a compound of the present invention as an active ingredient. A compound of the present invention may also be administered as a bolus, electuary or paste. [0273] In solid dosage forms of the invention for oral administration (capsules, tablets, pills, dragees, powders, granules, trouches and the like), the active ingredient is mixed with one or more pharmaceutically-acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: (1) fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose and/or acacia; (3) humectants, such as glycerol; (4) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; (5) solution retarding agents, such as paraffin; (6) absorption accelerators, such as quaternary ammonium compounds and surfactants, such as poloxamer and sodium lauryl sulfate; (7) wetting agents, such as, for example, cetyl alcohol, glycerol monostearate, and non- ionic surfactants; (8) absorbents, such as kaolin and bentonite clay; (9) lubricants, such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, zinc stearate, sodium stearate, stearic acid, and mixtures thereof; (10) coloring agents; and (11) controlled release agents such as crospovidone or ethyl cellulose. In the case of capsules, tablets and pills, the pharmaceutical compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-shelled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like. [0274] A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymethyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent. [0275] The tablets, and other solid dosage forms of the pharmaceutical compositions of the present invention, such as dragees, capsules, pills and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical- formulating art. They may also be formulated so as to provide slow or controlled release of the active ingredient therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile, other polymer matrices, liposomes and/or microspheres. They may be formulated for rapid release, e.g., freeze-dried. They may be sterilized by, for example, filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved in sterile water, or some other sterile injectable medium immediately before use. These compositions may also optionally contain opacifying agents and may be of a composition that they release the active ingredient(s) only, or preferentially, in a certain portion of the gastrointestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes. The active ingredient can also be in micro-encapsulated form, if appropriate, with one or more of the above-described excipients. [0276] Liquid dosage forms for oral administration of the compounds of the invention include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active ingredient, the liquid dosage forms may contain inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. [0277] Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, coloring, perfuming and preservative agents. [0278] Suspensions, in addition to the active compounds, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof. [0279] Formulations of the pharmaceutical compositions of the invention for rectal or vaginal administration may be presented as a suppository, which may be prepared by mixing one or more compounds of the invention with one or more suitable nonirritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, and which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the rectum or vaginal cavity and release the active compound. [0280] Formulations of the present invention which are suitable for vaginal administration also include pessaries, tampons, creams, gels, pastes, foams or spray formulations containing such carriers as are known in the art to be appropriate. [0281] Dosage forms for the topical or transdermal administration of a compound of this invention include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches and inhalants. The active compound may be mixed under sterile conditions with a pharmaceutically-acceptable carrier, and with any preservatives, buffers, or propellants which may be required. [0282] The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof. [0283] Powders and sprays can contain, in addition to a compound of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane. [0284] Transdermal patches have the added advantage of providing controlled delivery of a compound of the present invention to the body. Such dosage forms can be made by dissolving or dispersing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate of such flux can be controlled by either providing a rate controlling membrane or dispersing the compound in a polymer matrix or gel. [0285] Ophthalmic formulations, eye ointments, powders, solutions and the like, are also contemplated as being within the scope of this invention. [0286] Pharmaceutical compositions of this invention suitable for parenteral administration comprise one or more compounds of the invention in combination with one or more pharmaceutically-acceptable sterile isotonic aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain sugars, alcohols, antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents. [0287] Examples of suitable aqueous and nonaqueous carriers which may be employed in the pharmaceutical compositions of the invention include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants. [0288] These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms upon the subject compounds may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin. [0289] In some cases, in order to prolong the effect of a drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material having poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally- administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle. [0290] Injectable depot forms are made by forming microencapsule matrices of the subject compounds in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of drug to polymer, and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissue. [0291] When the compounds of the present invention are administered as pharmaceuticals, to humans and animals, they can be given per se or as a pharmaceutical composition containing, for example, 0.1 to 99% (more preferably, 10 to 30%) of active ingredient in combination with a pharmaceutically acceptable carrier. [0292] The preparations of the present invention may be given orally, parenterally, topically, or rectally. They are of course given in forms suitable for each administration route. For example, they are administered in tablets or capsule form, by injection, inhalation, eye lotion, ointment, suppository, etc. administration by injection, infusion or inhalation; topical by lotion or ointment; and rectal by suppositories. Oral administrations are preferred. [0293] The phrases “parenteral administration” and “administered parenterally” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal and intrasternal injection and infusion. [0294] The phrases “systemic administration,” “administered systemically,” “peripheral administration” and “administered peripherally” as used herein mean the administration of a compound, drug or other material other than directly into the central nervous system, such that it enters the patient’s system and, thus, is subject to metabolism and other like processes, for example, subcutaneous administration. [0295] These compounds may be administered to humans and other animals for therapy by any suitable route of administration, including orally, nasally, as by, for example, a spray, rectally, intravaginally, parenterally, intracisternally and topically, as by powders, ointments or drops, including buccally and sublingually. [0296] Regardless of the route of administration selected, the compounds of the present invention, which may be used in a suitable hydrated form, and/or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically-acceptable dosage forms by conventional methods known to those of skill in the art. [0297] Actual dosage levels of the active ingredients in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient. [0298] The selected dosage level will depend upon a variety of factors including the activity of the particular compound of the present invention employed, or the ester, salt or amide thereof, the route of administration, the time of administration, the rate of excretion or metabolism of the particular compound being employed, the rate and extent of absorption, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compound employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts. [0299] A physician or veterinarian having ordinary skill in the art can readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian could start doses of the compounds of the invention employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved. [0300] In general, a suitable daily dose of a compound of the invention will be that amount of the compound which is the lowest dose effective to produce a therapeutic effect. Such an effective dose will generally depend upon the factors described above. Preferably, the compounds are administered at about 0.01 mg/kg to about 200 mg/kg, more preferably at about 0.1 mg/kg to about 100 mg/kg, even more preferably at about 0.5 mg/kg to about 50 mg/kg. When the compounds described herein are co-administered with another agent (e.g., as sensitizing agents), the effective amount may be less than when the agent is used alone. [0301] If desired, the effective daily dose of the active compound may be administered as two, three, four, five, six or more sub-doses administered separately at appropriate intervals throughout the day, optionally, in unit dosage forms. Preferred dosing is one administration per day. [0302] The invention further provides a unit dosage form (such as a tablet or capsule) comprising a piperidinyl-methylpurine benzene or related compound described herein in a therapeutically effective amount for the treatment of a disease or condition described herein. EXAMPLES [0303] The invention now being generally described, will be more readily understood by reference to the following examples, which are included merely for purposes of illustrating certain aspects and embodiments of the present invention, and are not intended to limit the invention. Abbreviations used include: equiv or eq: molar equivalents; DCM: dichloromethane; DMF: dimethylformamide; DMAc: dimethylacetamide; DMSO: dimethylsulfoxide; DIPEA: diisopropylethylamine; IPA: isopropyl alcohol; and PdC1 ₂ (dppf): bis(diphenylphosphino)ferrocene]dichloropalladium(II). Example 1 – Synthesis of (S)-1-((R)-3-amino-1-(3-((6-amino-9H-purin-9-yl)methyl)-5-(2 ,5- difluoro-4-methoxyphenyl)pyridin-2-yl)piperidin-3-yl)-2,2-di fluoroethan-1-ol (II-1) [0304] The title compound was prepared according to the following procedures.

Step 1: Synthesis of Compound C [0305] Compound A (3.00 g, 1.0 equiv.) was combined with compound B (1.3 equiv.) in 10 volumes of 1,4-dioxane. Cs ₂ CO ₃ (1.5 equiv) and PdCl ₂ (dppf) ●DCM (0.05 equiv.) were charged and the mixture refluxed for 16 hours to generate compound C. Step 2: Synthesis of Compound E [0306] Compound C (2.00g, 1.0 equiv.) and D (2.0 equiv.) were combined in 10 volumes of DMSO with DIPEA (6 equiv.) and heated to 120 ºC for 4 hours to generate compound E. Step 3: Synthesis of Compound F [0307] Compound E (3.60 g, 1.0 equiv) was reduced using LiBH4 (5.0 equiv.) in 10 volumes of THF at 0 ºC. Then, reaction was warmed to room temperature and stirred for 16 hours to providde compound F. Step 4: Synthesis of Compound G [0308] Compound F (1.20 g, 1.0 equiv) was reacted with SOCl ₂ (2.0 equiv) in 5 volumes of DMAc with DMF (0.1 equiv) at 0 ºC, and then allowed to warm to room temperature and stir for 3 hours to generate compound G. Step 5: Synthesis of Compound I [0309] Compound G (1.20 g, 1.0 equiv) was charged with 10 volumes of DMF and compound H (1.0 equiv). To the resulting mixture, K ₂ CO ₃ (3.0 equiv) was added at 0 ºC, and then the mixture was warmed to room temperature and stirred for 12 hours. The resulting crude mixture was then exposed to 20 volumes of 1M HC1 in 20 volumes of 1,4-dioxane at 60 ºC for 16 hours to provide compound I. Step 6: Synthesis of II-1 [0310] Compound I (900 mg, 1.0 equiv) was charged with 10 volumes of methanol, then Pd/C (10%, 0.1 equiv), under hydrogen gas for 16 hours to generate compound II-1. ¹ H NMR (DMSO- d ₆ , 400 MHz): 8.37 (s, 1H), 8.25 (s, 1H), 8.12 (s, 1H), 7.39 (dd, J = 11.6, 7.2 Hz, 1H), 7.26 (br s, 2H), 7.18 (dd, J = 12.0, 7.6 Hz, 1H), 6.17 (t, J = 54.8 Hz, 1H), 5.48 (s, 2H), 3.84 (s, 3H), 3.70-3.66 (m, 2H), 3.17-3.09 (m,3H), 2.99-2.85 (m, 2 H), 1.91 (br s, 4H), 1.76-1.37 (m, 2H), 1.49 (br s, 1H). ¹ H NMR (DMSO-d6, 400 MHz): 8.37 (s, 1H), 8.31 (s, 1H), 8.16 (s, 1H), 7.39-7.34 (m, 2H), 7.14 (dd, J = 12.4, 7.6 Hz, 1H), 6.20 (t, J = 56.0 Hz, 1H), 5.52 (s, 2H), 3.84 (s, 3H), 3.19-3.11 (m,2H), 2.95-2.87 (m, 1 H), 1.91-1.68 (m, 7H). MS (ESI+): [M+H] ⁺ = 547.35. Example 2 – Synthesis of (S)-1-((R)-3-amino-1-(2-((6-amino-9H-purin-9-yl)methyl)-6-(2 ,5- difluoro-4-methoxyphenyl)pyridin-3-yl)piperidin-3-yl)-2,2-di fluoroethan-1-ol (III-1) [0311] The title compound was prepared according to the following procedures.

I III-1

Step 1 : Synthesis of Compound C

[0312] Compound A (3.00 g, 1.0 equiv.) was combined with compound B (1.3 equiv.) in 10 volumes of 1,4-dioxane. To the resulting mixture, CS ₂ CO ₃ (1.5 equiv) and PdC1 ₂ (dppf)●DCM (0.05 equiv.) were added, and the resulting mixture was refluxed for 4 hours to generate compound C. Step 2: Synthesis of Compound E [0313] Compound C (2.00g, 1.0 equiv.) and D (compound 1.7 equiv.) were combined in 10 volumes of DMSO with K2CO3 (2.0 equiv) and the resulting mixture was heated to 120 ºC for 5 hours to generate compound E. Step 3: Synthesis of Compound F [0314] Compound E (3.3 g, 1.0 equiv) was reduced using LiBH ₄ (10.0 equiv.) in 10 volumes of THF at 0 ºC. Then, the reaction was warmed to room temperature and stirred for 16 hours to generate compound F. Step 4: Synthesis of Compound G [0315] Compound F (3.0 g, 1.0 equiv) was reacted with SOCl2 (2.0 equiv) in 10 volumes of DCM at 0 ºC. Then, the mixture was allowed to warm to room temperature and stirred for 12 hours to generate compound G. Step 5: Synthesis of Compound I [0316] Compound G (3.10 g, 1.0 equiv) was charged with 10 volumes of DMF and compound H (1.0 equiv). To the resulting mixture, K ₂ CO ₃ (3.0 equiv) was added at 0 ºC, and then the mixture was warmed to room temperature and stirred for 12 hours. The resulting crude mixture was then exposed to 20 volumes of 1M HCl in 20 volumes of 1,4-dioxane at 60 ºC for 16 hours to generate compound I. Step 6: Synthesis of Compound III-1 [0317] Compound I (3.0 g, 1.0 equiv) was charged with 10 volumes of methanol, then Pd/C (10%, 0.1 equiv), under hydrogen gas for 20 hours to generate compound III-1. ¹ H NMR (DMSO-d ₆ , 400 MHz): 8.29-8.27 (m, 2H), 8.10 (s, 1H), 7.71 (br d, J = 7.2 Hz, 1H), 7.65 (d, 8.8 Hz, 1H), 7.19 (dd, J = 12.4, 7.2 Hz, 1H), 7.14 (dd, J = 12.8, 7.2 Hz, 1H), 6.23 (td, J = 55.2, 3.2 Hz, 1H), 5.69 (d, J = 16.4, 1H), 5.63 (d, J = 16.4 Hz, 1H), 3.86 (s, 3H), 3.06-2.99 (m, 2H), 2.86-2.82 (m, 2H), 1.97- 1.91 (m, 1H), 1.82-1.77 (m, 2H), 1.64-1.62 (m, 1H). MS (ESI+): [M+H] ⁺ = 547.7. Example 3 – Synthesis of (S)-1-((R)-3-amino-1-(3-((6-amino-9H-purin-9-yl)methyl)-2',5 '- difluoro-4'-methoxy-[1,1'-biphenyl]-4-yl)piperidin-3-yl)-2,2 -difluoroethan-1-ol (I-1) [0318] The title compound was prepared according to the following procedures. Step 1: Synthesis of Compound C [0319] Compound A (3.00 g, 1.0 equiv.) was combined with compound B (1.2 equiv.) in 10 volumes of DMSO with DIPEA (5.0 equiv), and the resulting mixture was heated to 120 ºC for 5 hours to generate compound C. Step 2: Synthesis of Compound E [0320] Compound C (2.20 g, 1.0 equiv.) and compound D (1.3 equiv.) were combined in 10 volumes of 1,4-dioxane. To this mixture, Cs ₂ CO ₃ (1.5 equiv) and PdCl ₂ (dppf) ●DCM (0.05 equiv.) were added, and the resulting mixture was refluxed for 6 hours to generate compound E. Step 3: Synthesis of Compound F [0321] Compound E (2.80 g, 1.0 equiv) was reduced using LiBH ₄ (10.0 equiv.) in 10 volumes of THF at 0 ºC. Then, the reaction mixture was warmed to room temperature and stirred for 16 hours to generate compound F. Step 4: Synthesis of Compound G [0322] Compound F (1.4 g, 1.0 equiv) was reacted with SOCl ₂ (3.0 equiv) in 5 volumes of DMAc with 0.1 volumes of DMF at 0 ºC, and then the reaction mixture was allowed to warm to room temperature and stirred for 3 hours to generate compound G. Step 5: Synthesis of Compound I [0323] Compound G (1.4 g, 1.0 equiv) was charged with 10 volumes of DMF and H (1.0 equiv). To this mixture, K ₂ CO ₃ (3.0 equiv) was added at 0 ºC, and then the reaction mixture was warmed to room temperature and stirred for 12 hours to generate compound I. Step 6: Synthesis of Compound J [0324] Crude compound I was exposed to 20 volumes of 1M HCl in 20 volumes of 1,4-dioxane at 60 ºC for 16 hours to generate compound J. Step 7: Synthesis of Compound I-1 [0325] Compound J (1.1 g, 1.0 equiv) was charged with 10 volumes of methanol, then Pd/C (10%, 0.1 equiv), under hydrogen gas for 20 hours to generate compound I-1. ¹ H NMR (CD ₃ OD, 400 MHz): 8.21 (s, 1H), 8.10 (s, 1H), 7.42 (br d, J = 8.8 Hz, 1H), 7.29 (d, J = 8.4 Hz, 1H), 7.11 (dd, J = 12.0, 7.6 Hz, 1H), 6.88 (dd, J = 12.0, 7.2 Hz, 1H), 6.04 (td, J = 54.0, 2.4 Hz, 1H), 5.54 (d, 15.2 Hz, 1H), 5.40 (d, J = 15.6 Hz, 1H), 3.79 (s, 3H), 3.58-3.52 (m, 1H), 2.78-2.64 (m, 3H), 1.93-1.88 (m, 1H), 1.71-1.64 (m, 2H). MS (ESI+): [M+H] ⁺ = 546.05. Example 4 – Evalution of NSD2 Inhibitory Activity for Exemplary Compounds [0326] Exemplary compounds were tested for NSD2 inhibitory activity using a modified RBC HotSpot HMT Assay. Experimental procedures and results are provided below. Part I – Experimental Procedures [0327] A reaction mixture was prepared by adding oligonucleosomes from Chicken (0.05 mg/ml) to freshly prepared reaction buffer containing 50 mM Tris-HCl (pH 8.5), 50 mM NaCl, 5 mM MgCl ₂ , 0.01% Brij35, 1 mM DTT, and 1% DMSO followed by the addition of recombinant human NSD2, (amino acids 2-end) with N-terminal His tag (2 nM; GenBank Accession No. NM_001042424; MW=155.5 kDa; expressed in Sf9 insect cells) and gentle mixing. The test compounds were diluted in DMSO, added to the reaction mixture in nanoliter amounts by using Acoustic Technology (Echo 550, LabCyte Inc. Sunnyvale, CA) and incubated for 20 minutes at room temperature. The reaction was initiated by the addition of S-Adenosyl-L-[methyl- ³ H] methionine ( ³ H-SAM; 1 µM), and the mixture was incubated for 1 hour at 30°C. The reaction mixture was delivered to filter paper and the methylated substrate was quantified by scintillation counting. Data analysis was performed using Excel and GraphPad Prism software for IC ₅₀ curve fits. For additional information on the histone methyltransferase assay, see, for example, Horiuchi KY, et al., “Assay Development for Histone Methyltransferases,” Assay Drug Dev Technol.2013 May;11(4):227-36. Part II – Results [0328] The results of the NSD2 inhibitory assay are reported in Table 5 below. The symbol +++ indicates an IC ₅₀ between 0.001 µM and 0.01 µM. The symbol ++ indicates an IC ₅₀ between 0.01 µM and 1 µM. The symbol + indicates an IC50 greater than 1 µM. Table 5. INCORPORATION BY REFERENCE [0329] The entire disclosure of each of the patent documents and scientific articles referred to herein is incorporated by reference for all purposes. EQUIVALENTS [0330] The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative rather than limiting the invention described herein. Scope of the invention is thus indicated by the appended claims rather than by the foregoing description, and all changes that come within the meaning and range of equivalency of the claims are intended to be embraced therein.