CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to and the benefit of U.S. Provisional Application No. 61/693,108 filed August 24, 2012, and U.S. Application No. 13/974,642 filed August 23, 2013, the disclosures of both of which applications are hereby incorporated herein by reference in their entirty.

TECHNICAL FIELD

This presently disclosed embodiments relate generally to the discovery of pro-neurogenic compounds capable of promoting neurogenesis and/or reducing neuronal cell death.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

This invention was made with government support under Grant Numbers 5DP1OD00027605,

5R37MH05938809, and 1RO1MH087986, which were awarded by the National Institute of Health; the Government has certain rights in the invention.

BACKGROUND

It is now accepted that the adult vertebrate brain fosters the birth and functional incorporation of newly formed neurons (Goldman and Nottebohm, Proc Natl Acad Sci USA 1983, 80: 2390-2394; Paton and Nottebohm, Science 1984, 225, 1046-1048; Burd and Nottebohm, J Comp Neurol 1985, 240: 143- 152). However, it was long thought that no new neurons could be added to the adult mammalian brain. This dogma was challenged in the 1960's when autoradiographic evidence of new neuron formation in the hippocampal dentate gyrus, olfactory bulb, and cerebral cortex of the adult rat was presented (Altman, J. Science 1962, 135, 1127- 1128; Altman, J. J Comp Neurol 1966, 128:431-474; Altman, Anat Rec 1963, 145:573-591 ; Altman and Das, J. Comp. Neurol. 1965, 124, 319-335; Altman and Das, J Comp Neurol 1966, 126:337-390). It is now accepted that within all mammalian species, including humans (Eriksson et al., Nat. Med. 1998, 4(11), 1313-1317), there are two major reservoirs of neuronal stem cells, one located in the subgranular zone (SGZ) of the hippocampal dentate gyrus and another in the subventricular zone (SVZ) (Gross, Natl. Rev. 2000, 1, 67-72). Neural stem cells in the SVZ facilitate formation of new neurons that migrate rostrally to populate the olfactory bulb, while neural stem cells in the SGZ produce neurons that integrate locally in the granular layer of the dentate gyrus, a region of the hippocampus that exhibits lifelong structural and functional plasticity.

The process of new neuron formation in the adult mouse brain can be influenced by

environmental, chemical and genetic variables. As demonstrated by Gage and colleagues, neurogenesis in the adult mouse brain is enhanced when animals are exposed to an enriched environment (Kempermann et al., Nature 1997, 386, 493-495) or able to exercise voluntarily (van Praag et al., Nat. Neuro-sci. 1999, 2, 266-270). More recently, anti-depressant drugs have been shown to enhance levels of adult neurogenesis in animals, including humans (Schmidt et al., Behav Pharmacol. 2007 Sep; 18(5-6):391-418; Boldrini et al., Neuropsychopharmacology 2009, 34, 2376-2389). Among many genes reported to impact adult neurogenesis is the gene encoding neuronal PAS domain protein 3 (NPAS3), a central nervous system (CNS)-specific transcription factor that has been associated with schizophrenia and bipolar disorder (Kamnasaran et al., J. Med. Genet. 2003, 40, 325-332; Pickard et al., Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2005, 136B, 26-32; Pickard et al., Ann. Med. 2006, 38, 439-448; Pickard et al., Mol. Psychiatry 2009, 14, 874-884; Lavedan et al., Pharmacogenomics 2008, 9: 289-301). Animals missing both copies of the NPAS3 gene suffer a profound loss of adult hippocampal neurogenesis coupled with significant behavioral deficits (Pieper et al., Proc. Natl. Acad. Sci. USA 2005, 102, 14052-14057). Knowing that impaired post-natal neurogenesis elicits unfavorable phenotypic deficits, it is predicted that pro-neurogenic chemical compounds should exhibit favorable therapeutic benefits.

SUMMARY

The presently disclosed embodiments relate generally to compounds that promote the generation or the survival of existing neurons in the mammalian brain. For the purpose of simplicity these compounds are referred to as being pro-neurogenic. In certain embodiments, the compounds promote the generation or survival of neurons in the post-natal mammalian brain. In certain embodiments, the compounds promote the survival, growth, development and/or function of neurons, particularly CNS, brain, cerebral, and hippocampal neurons. In certain embodiments, the compounds stimulate post-natal hippocampal neurogenesis, which while not wishing to be bound by theory, is believed to represent a therapeutic target for a variety of neuropsychiatric and neurodegenerative diseases, including (but not limited to) schizophrenia,major depression, bipolar disorder, normal aging, epilepsy, traumatic brain injury, post-traumatic stress disorder, Parkinson's disease, Alzheimer's disease, Down syndrome, spinocerebellar ataxia, amyotrophic lateral sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, abuse of neuro-active drugs (such as alcohol, opiates, methamphetamine, phencyclidine, and cocaine), retinal degeneration, spinal cord injury, and peripheral nerve injury. In certain

embodiments, the compounds stimulate post-natal hypothalamic neurogenesis, which can provide therapeutic benefits in weight management, such as physiological weight loss associated with various conditions, including but not limited to, normal aging, chemotherapy, radiation therapy, stress, drug abuse, anorexia, as well as other diseases discussed herein.

In an aspect, compounds of the presently disclosed embodiments may include those represented by formula (I):

wherein:

R ² and R ³ , together with CI and C2, form the optionally substituted phenyl, pyridine or pyrimidine ring of formulas (II)-(IV) described below, or are defined as R ^2d and R ^3d of formula (V), respectively;

R ⁴ is defined as any one of R ^4a -R ^4d in formulas (II)-(IV); and

n is 0 or 2.

For example, a compound or pharmaceutically acceptable salt thereof, for promoting

neurogenesis and/or reducing neuronal cell death, can be represented by formula (II):

wherein R ^la is selected from the group consisting of: -CH ₂ -C(0)-Z ^la and -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ - Z ^2a ; and

R ^3a and R ^4a are each independently selected from the group consisting of: hydrogen, halo, hydroxyl, Q_3 alkoxyl, cyano, carboxyl, and formamide;

wherein Z ^la is selected from the group consisting of: hydroxyl; Q_6 alkoxyl; amine optionally substituted with 1 or more Q_i ₂ alkyl, C ₂ _i ₂ alkenyl, C3_i ₂ cycloalkyl, Ci_i ₂ sulfonyl optionally substituted with 1-6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo, C4_i ₂ heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂ _i ₂ carbonyl optionally substituted with 1-6 halo, and/or C ₂ _i ₂ carboxyalkyl optionally substituted with 1-6 halo; C _{2 2} heterocyclyi; C ₆ _i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; wherein one of R and R is hydroxyl, halo, or amine optionally substituted with 1 or more Q_6 alkyl, C ₂ -6 alkenyl, C3.6 cycloalkyl, C ₂ -6 heterocyclyl, e-u aryl, and/or C ₄₄₂ heteroaryl; and the other of R ^A1 and R ^A2 is hydrogen;

wherein Z ^2a is selected from the group consisting of: halo, 0(R ^a ), S(R ^b ) and N(R ^c )(R ^d ); wherein R ^a and R ^b are each independently selected from the group consisting of: C1 2 alkyl; C ₂ - ₁₂ alkenyl; C3 2 cycloalkyl; C ₂ -6 heterocyclyl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl;

wherein R ^c and R ^d are each independently selected from the group consisting of:

hydrogen; C1 2 alkyl; C ₂ _i ₂ alkenyl; C ₃ _i ₂ cycloalkyl; C ₂ _6 heterocyclyl; C ₆ _i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; and Cz _t _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; or wherein R ^c and R ^d together with the nitrogen they are attached to form a C _4- i ₄ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or Ci_6 alkoxyl.

In some embodiments, one or more of the following definitions apply:

(1) R ^3a and R ^4a are both hydro gen or both bromo;

(2) Z ^la is hydroxyl or amine optionally substituted with 1 or more C142 alkyl, C ₂ - ₁₂ alkenyl,

and/or C _{3 2} cycloalkyl;

(3) one of R ^A1 and R ^A2 is hydroxyl or halo; and the other of R ^A1 and R ^A2 is hydrogen;

(4) Z ^2a is 0(R ^a ) or S(R ^b ); and/or

(5) Z ^2a is N(R ^c )(R ^d ). For example, R ^la may be -CH ₂ -C(0)-Z ^la or -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2a .

When R ^la is -CH ₂ -C(0)-Z ^la , Z ^la may be hydroxyl or d_ ₆ alkoxyl. Z ^la may also be amine optionally substituted with 1 or more Q42 alkyl, C ₂ _i ₂ alkenyl, C ₃ _i ₂ cycloalkyl, Ci_i ₂ sulfonyl optionally substituted with 1-6 halo, C _{6 2} aryl sulfonyl optionally substituted with 1-6 halo, C442 heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂₄₂ carbonyl optionally substituted with 1-6 halo, and/or C242 carboxyalkyl optionally substituted with 1-6 halo. For example, Z ^la can be amine optionally substituted with 1 or more Q ₄₂ alkyl, C ₂₄₂ alkenyl, and/or C ₃₄₂ cycloalkyl. Z ^la may also be C ₂₄₂ heterocyclyl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; or C ₄₄₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl.

When R ^la is -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2a , both of R ^A1 and R ^A2 can be hydrogen. Alternatively, one of R ^A1 and R^ is hydroxyl, halo (e.g., fluoro), or amine optionally substituted with 1 or more Ci_6 alkyl (e.g., methyl), C ₂ -6 alkenyl, C3.6 cycloalkyl, C ₂ -6 heterocyclyl, C6-i ₂ aryl, and/or C4_i ₂ heteroaryl; and the other of R ^A1 and R ^A2 is hydrogen. Z ^2a can be halo, 0(R ^a ), S(R ^b ) or N(R ^c )(R ^d ). R ^a and R ^b are each common substitutients such as: C n alkyl; C ₂ - ₁₂ alkenyl; C _{3 2} cycloalkyl; C ₂ -6 heterocyclyl; Ce-^ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; and C _{4 2} heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl. R ^c and R ^d can both be hydrogen or each common substitutients such as: C n alkyl; C ₂ - ₁₂ alkenyl; C3 ₂ cycloalkyl; C ₂ -6 heterocyclyl; Ce-n aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl.

Alternatively, R ^c and R ^d together with the nitrogen they are attached to can form a ring structure, such as a C ₄ _i4 heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl.

R ^3a may be hydrogen, halo (e.g., bromo), hydroxyl, Q_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^3a is hydrogen. In some embodiments, R ^3a is bromo.

R ^4a may be hydrogen, halo (e.g., bromo), hydroxyl, Q_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^4a is hydrogen. In some embodiments, R ^4a is bromo.

In certain embodiments, the presently disclosed embodiments include a compound or pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the compound having formula (III):

b

(III) wherein R is selected from the group consisting of: hydrogen; Ci_6 alkyl optionally substituted with 1 or more halo, hydroxyl, cyano and/or azide; -CH(R ⁵ )-C(0)-Z ^lb ; and -CH ₂ -C(R ^A1 )(R ^A2 )- CH ₂ -Z ^2b ;

wherein R ⁵ is hydrogen or Ci_3 alkyl;

wherein one of R and R is hydroxyl or halo and the other is hydrogen; wherein Z is selected from the group consisting of: hydroxyl; Q_6 alkoxyl; and amine optionally substituted with a hydroxyl, C1 2 sulfonyl optionally substituted with 1-6 halo, Ce-12 aryl sulfonyl optionally substituted with 1-6 halo, C _{4 2} heteroaryl sulfonyl optionally substituted with 1 -6 halo, C ₂ -i ₂ carbonyl optionally substituted with 1 -6 halo, and/or C ₂ - ₁₂ carboxyalkyl optionally substituted with 1 -6 halo;

wherein Z ^2b is selected from the group consisting of: Q_3 alkyl, azide, and N(R ⁶ )(R ⁷ ); wherein R ⁶ and R ⁷ are each independently selected from the group consisting of:

hydrogen; carboxamide optionally substituted with 1 or more Ci_6 alkyl, Ce-n aryl and/or Czt_i ₂ heteroaryl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_ ₆ alkoxyl; Ci_i ₂ sulfonyl optionally substituted with 1 -6 halo; C ₆ _i ₂ aryl sulfonyl optionally substituted with 1 -6 halo; and C ₄ _i ₂ heteroaryl sulfonyl optionally substituted with 1 -6 halo; wherein no more than one of R ⁶ and R ⁷ is hydrogen; and wherein R ^3b and R ^4b are each independently selected from the group consisting of: hydrogen, halo, hydroxyl, Ci_3 alkoxyl, cyano, carboxyl, and formamide.

In some embodiments, one or more of the following definitions apply:

(1) when R ^lb is optionally substituted Ci_6 alkyl, R ^lb is selected from unsubstituted Ci_6 alkyl or C3_6 alkyl substituted with 1 hydroxyl or Ci_6 alkyl substituted with 1 cyano;

(2) when R ^lb unsubstituted Ci_6 alkyl, R ^lb is unsubstituted C ₂ -6 alkyl;

(3) when R ⁵ is hydrogen, Z ^lb is amine optionally substituted with a hydroxyl, sulfonyl optionally substituted with 1 -6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1 -6 halo, C4 2 heteroaryl sulfonyl optionally substituted with 1 -6 halo, C ₂ -i ₂ carbonyl optionally substituted with 1 -6 halo, and/or C ₂ - ₁₂ carboxyalkyl optionally substituted with 1 -6 halo; and/or

(4) Z ^2b is azide or N(R ⁶ )(R ⁷ ).

For example, R may be hydrogen. R may also be Ci_6 alkyl optionally substituted with 1 or more halo, hydroxyl, cyano and/or azide, such as unsubstituted Ci_6 alkyl (e.g., methyl, ethyl, n-propyl, isopropyl, or tert-butyl) or C ₃ _ ₆ alkyl substituted with 1 hydroxyl (e.g., at the beta-carbon) or Ci_ ₆ alkyl substituted with 1 cyano. R ^lb may also be -CH(R ⁵ )-C(0)-Z ^lb or -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2b .

R ⁵ can be hydrogen or Ci_ ₃ alkyl (e.g., methyl). Z ^lb can be hydroxyl or Ci_ ₆ alkoxyl. Z ^lb can also be amine optionally substituted with 1 hydroxyl, or amine optionally substituted with C1 2 sulfonyl, C ₆ _i ₂ aryl sulfonyl, C _4- i2 heteroaryl sulfonyl, C ₂ -i ₂ carbonyl, or C ₂ - ₁₂ carboxyalkyl (e.g., -CH ₂ C(0)OH). The Ci_ ₁₂ sulfonyl, e-u aryl sulfonyl, heteroaryl sulfonyl, C ₂ - ₁₂ carbonyl, and C ₂ - ₁₂ carboxyalkyl groups can contain one or more common substitutients such as alkyl, halo, hydroxyl, alkoxyl, aryl and/or heteroaryl.

One of R ^A1 and R ^A2 can be hydroxyl or halo (e.g., fluoro) and the other of R ^A1 and R^ can be hydrogen. Alternatively, both R ^A1 and R ^A2 can be hydrogen. Z ^2b can be Q_3 alkyl. Z ^2b can also be azide or N(R ⁶ )(R ⁷ ). R ⁶ and R ⁷ can both be hydrogen. Alternatively, only one of R ⁶ and R ⁷ is hydrogen, or none of R ⁶ and R ⁷ is hydrogen. R ⁶ and R ⁷ can also be carboxamide optionally substituted with 1 or more Q_6 alkyl, C6-i ₂ aryl and/or C4 2 heteroaryl; C6-i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_ ₆ alkoxyl; C n sulfonyl optionally substituted with 1-6 halo; C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo; or C4 2 heteroaryl sulfonyl optionally substituted with 1-6 halo.

R ^3b may be hydrogen, halo (e.g., bromo), hydroxyl, Ci_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^3b is hydrogen. In some embodiments, R ^3b is bromo.

_R 4b

may be hydrogen, halo (e.g., bromo), hydroxyl, Ci_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^4b is hydrogen. In some embodiments, R ^4b is bromo.

For example, both R ^3b and R ^4b are hydrogen. Both R ^3b and R ^4b can be bromo.

In certain embodiments, the presently disclosed embodiments include a compound or

pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the compound having formula (IV):

wherein:

R ^lc is selected from the group consisting of: hydrogen, Ci_6 alkyl, Ci_ ₆ carboxyalkyl, Ci_i2 sulfonyl optionally substituted with 1-6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo and Cz _t _i2 heteroaryl sulfonyl optionally substituted with 1-6 halo;

R ^2c is selected from the group consisting of: hydrogen; hydroxyl; cyano; halo; amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl; and Q_ 12 alkoxyl;

R ^3c is selected from the group consisting of: carboxyl; Ci_ ₆ alkoxycarbonyl; hydroxyl; Ci_i ₂ alkoxyl; cyano; halo; and amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl;

R ^4c is selected from the group consisting of: hydrogen, halo, hydroxyl, and Q_3 alkoxyl; and one or both of Qi and (¾ are nitrogen.

In some embodiments, one or more of the following definitions apply:

(1) R ^2c is hydrogen; hydroxyl; or C1 2 alkoxyl; and/or (2) R ^c is carboxyl; Ci_6 alkoxycarbonyl; hydroxyl; or amine substituted with 1-2 Ci_6 alkyl.

For example, R ^lc can be hydrogen. R ^lc can also be Ci_6 alkyl or C ₂ -6 carboxyalkyl (e.g., - CH ₂ C(0)OH). R ^lc can also be C1 2 sulfonyl optionally substituted with 1-6 halo or e-u aryl sulfonyl (e.g., -S(0) ₂ Ph) optionally substituted with 1-6 alkyl, substituted alkyl (e.g., CF ₃ ) and/or halo. R ^lc can also be C4 2 heteroaryl sulfonyl optionally substituted with 1-6 alkyl, substituted alkyl (e.g., CF ₃ ) and/or halo.

R ^2c can be hydrogen or hydroxyl. R ^2c can also be cyano; halo; or amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl. R ^c can also be C 1-12 alkoxyl.

R ^3c can be carboxyl or Ci_ ₆ alkoxycarbonyl (e.g., -C(0)OCH ₃ or -C(0)OCH ₂ CH ₃ ). R ^3c can also be hydroxyl. R ^3c can also be alkoxyl; cyano; or halo (e.g., bromo). R ^3c can also be amine optionally substituted with 1 or more Q_6 alkyl, C ₂ -6 alkenyl, C ₃ _6 cycloalkyl, aryl, and/or heteroaryl, such as N(CH ₃ ) ₂ .

R ^4c can be hydrogen or halo (e.g., bromo). R ^4c can also be hydroxyl or and Q_ ₃ alkoxyl.

Qi and Q ₂ can both be nitrogen. Alternatively, one of Qi and Q ₂ is nitrogen and the other of Qi and Q ₂ is carbon. In some embodiments, when both Qi and Q ₂ are be nitrogen and both R ^2c and R ^3c are hodroxyl, the corresponding ring structure is typically represented by:

In certain embodiments, the presently disclosed embodiments include a compound or pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the

(V)

wherein R ^ld is selected from the group consisting of: hydrogen and CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ - N(R ⁶ )(R ⁷ );

wherein one of R ^A1 and R ^A2 is hydroxyl or halo and the other is hydrogen; and wherein R ⁶ and R ⁷ are each independently selected from the group consisting of:

hydrogen; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; and Czt_i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or Ci_6 alkoxyl;

wherein R ^2d is selected from the group consisting of: halo, hydroxyl, C1 2 alkoxyl, cyano, aryl, and heteroaryl;

wherein R ^3d is selected from the group consisting of: hydrogen and amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _ ₆ alkenyl, C ₃ _ ₆ cycloalkyl, C ₂ _ ₆ heterocyclyl, aryl, and/or heteroaryl; and

wherein R ^4d is selected from the group consisting of: hydrogen, halo, hydroxyl, and Ci_ ₃ alkoxyl.

In some embodiments, R ^2d is cyano, and/or R ^4d is hydrogen, bromo or methoxy.

For example, R ^ld can be hydrogen. R ^ld can also be CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -N(R ⁶ )(R ⁷ ). One of R ^A1 and R ^A2 can be hydroxyl and the other is hydrogen. One of R ^A1 and R ^A2 can be halo (e.g., fluoro) and the other is hydrogen. Alternatively, both R ^A1 and R^ can be hydrogen. R ⁶ and R ⁷ can both be hydrogen.

Alternatively, one or both of R ⁶ and R ⁷ can be -u aryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or Ci_6 alkoxyl; or heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or Ci_6 alkoxyl.

R ^2d can be halo, hydroxyl, or Ci_i ₂ alkoxyl. R ^2d can also be cyano. R ^2d can also be aryl (e.g., Ce-

12) or heteroaryl (e.g., C ₄ -i ₂ ).

R ^3d can be hydrogen. R ^3d can also be amine optionally substituted with 1 or more Ci_6 alkyl, C ₂ _6 alkenyl, C ₃ _6 cycloalkyl, C ₂ _6 heterocyclyl, aryl (e.g., Ce-n), and/or heteroaryl (e.g., C _4- i2).

_R 4d

can be hydrogen, halo (e.g., bromo), hydroxyl, or Ci_ ₃ alkoxyl (e.g., methoxyl).

Compounds or salts thereof having any combinations of the the above definitions of the various groups are all included in the presently disclosed embodiments.

The presently disclosed embodiments also include compositions (e.g., pharmaceutical compositions) that include such compounds as well as methods of making, identifying, and using such compounds. Other features and advantages are described in, or will be apparent from, the present specification and accompanying drawings.

Any of the compounds disclosed herein can be used in any of the methods or compositions described anywhere herein. The presently disclosed embodiments relate generally to stimulating neurogenesis (e.g., post-natal neurogenesis, e.g., post-natal hippocampal and/or hypothalamic neurogenesis) and protecting neurons from death with a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein.

For example, methods of promoting the generation of neurons are featured. As another example, methods of promoting the survival, growth, development and/or function of neurons, particularly CNS, brain, cerebral, hippocampal and hypothalamic neurons are featured. As a further example, methods of stimulating post-natal hippocampal and/or hypothalamic neurogenesis are featured.

In some embodiments, such methods can include in vitro methods, e.g., contacting a sample (e.g., a cell or tissue) with a compound of any of the formulae described herein or a salt (e.g., a

pharmaceutically acceptable salt) thereof as defined anywhere herein. In other embodiments, the methods can include administering a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein to a subject (e.g., a mammal, such as a human).

Accordingly, in an aspect, the presently disclosed embodiments include and feature methods of screening for (thereby identifying) compounds that stimulate neurogenesis (e.g., post-natal neurogenesis, e.g., post-natal hippocampal and/or hypothalamic neurogenesis) or protect newborn neurons from cell death.

In another aspect, methods for treating (e.g., controlling, relieving, ameliorating, alleviating, or slowing the progression of) or methods for preventing (e.g., delaying the onset of or reducing the risk of developing) one or more diseases, disorders, or conditions caused by, or associated with insufficient (e.g., aberrant) neurogenesis or unwanted neuronal cell death in a subject in need thereof are featured. The methods include administering to the subject an effective amount of a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein to the subject.

In another aspect, the use of a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein in the preparation of, or for use as, a medicament for the treatment (e.g., controlling, relieving, ameliorating, alleviating, or slowing the progression of) or prevention (e.g., delaying the onset of or reducing the risk of developing) of one or more diseases, disorders, or conditions caused by, or associated with, insufficient (e.g., aberrant) neurogenesis or unwanted neuronal cell death is featured.

In some embodiments, the one or more diseases, disorders, or conditions can include

neuropathies, nerve trauma, and neurodegenerative diseases. In some embodiments, the one or more diseases, disorders, or conditions can be diseases, disorders, or conditions caused by, or associated with insufficient neurogenesis (e.g., aberrant hippocampal and/or hypothalamic neurogenesis) as is believed to occur in neuropsychiatric diseases, or aberrant neuronal cell death as is believed to occur in

neurodegenerative diseases. Examples of the one or more diseases, disorders, or conditions include, but are not limited to, schizophrenia, major depression, bipolar disorder, normal aging, epilepsy, traumatic brain injury, post-traumatic stress disorder, Parkinson's disease, Alzheimer's disease, Down syndrome, spinocerebellar ataxia, amyotrophic lateral sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, and abuse of neuro-active drugs (such as alcohol, opiates, methamphetamine,

phencyclidine, and cocaine), retinal degeneration, spinal cord injury, peripheral nerve injury, physiological weight loss associated with various conditions, and cognitive decline associated with normal aging, radiation therapy, and chemotherapy.

In some embodiments, the subject can be a subject in need thereof (e.g., a subject identified as being in need of such treatment, such as a subject having, or at risk of having, one or more of the diseases or conditions described herein). Identifying a subject in need of such treatment can be in the judgment of a subject or a health care professional and can be subjective (e.g. opinion) or objective (e.g. measurable by a test or diagnostic method). In some embodiments, the subject can be a mammal. In certain embodiments, the subject can be a human.

In some embodiments, methods of making the compounds described herein are featured. In embodiments, the methods include taking any one of the intermediate compounds described herein and reacting it with one or more chemical reagents in one or more steps to produce a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein.

In some embodiments, methods of making the pharmaceutical compositions described herein are featured. In embodiments, the methods include taking any one or more of the compounds of any of the other formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein, and mixing said compound(s) with one or more pharmaceutically acceptable carriers. In one aspect, kits for the treatment (e.g., controlling, relieving, ameliorating, alleviating, or slowing the progression of) or prevention (e.g., delaying the onset of or reducing the risk of developing) of one or more diseases, disorders, or conditions caused by, or associated with insufficient (e.g., aberrant) neurogenesis or unwanted neuronal cell death are featured. The kits include (i) a compound of any of the formulae described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein; and (ii) instructions that include a direction to administer said compound to a subject (e.g., a patient).

In various embodiments, compounds of formula (I), (II), (III), (IV) and (V) can be used in a method for the treatment of a disease, disorder, or condition caused by unwanted neuronal cell death or associated with insufficient neurogenesis in a subject in need thereof. The method can include administering to the subject an effective amount of a compound having formula (I), (II), (III), (VI), or (V) or a pharmaceutically acceptable salt thereof, as defined herein. The methods can further include detecting a resultant neurotrophism (e.g., neurogenesis; and/or determining that the patient has aberrant neurotrophism, particularly aberrant neurogenesis, particularly aberrant hippocampal and/or hypothalamic neurogenesis, or a disease or disorder associated therewith, particularly by detecting and/or diagnosing the same.

The methods can further include detecting determining that the subject has aberrant neurogenesis or death of neurons or a disease or disorder associated therewith, by detecting the same in said subject.

The methods can further include detecting a resultant hippocampal and/or hypothalamic neurogenesis. The compounds of the presently disclosed embodiments may be used to block neuron cell death in a manner that not only protects mature neurons, but also augments hippocampal neurogenesis by promoting survival of newborn neurons. In some embodiments, the compounds of the presently disclosed embodiments may have a pro-neurogenic activity that is attributable to their ability to impede the death of newborn hippocampal neurons. Instead of stimulating the birth of neuronal stem cells, the compounds may favor their post-birth survival along the differentiation pathway required for them to evolve into properly wired, granular neurons. In the absence of compound administration, upwards of 80% of newborn neurons die. Administration of the compounds of the presently disclosed embodiments can significantly enhance the survival of newborn hippocampal neurons in the adult brain.

The disease, disorder, or condition can be a neuropsychiatric and neurodegenerative disease, including (but not limited to) schizophrenia, major depression, bipolar disorder, normal aging, epilepsy, traumatic brain injury, post-traumatic stress disorder, Parkinson's disease, Alzheimer's disease, Down syndrome, spinocerebellar ataxia, amyotrophic lateral sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, and abuse of neuro-active drugs (such as alcohol, opiates, methamphetamine, phencyclidine, and cocaine), retinal degeneration, spinal cord injury, peripheral nerve injury, physiological weight loss associated with various conditions, and cognitive decline associated with normal aging, and chemotherapy.

In certain embodiments, the compounds of the presently disclosed embodiments can be used to treat a depressive disorder. For example, the compounds may augment ghrelin- induced hippocampal neurogenesis, thereby treating the depressice disorder. The depressive disorder can be associated with insufficient ghrelin response. In an embodiment, the insufficient ghrelin response may result in impaired or reduced hippocampal neurogenesis.

In some embodiments, the compounds or salt (e.g., a pharmaceutically acceptable salt) thereof provide at least about 27 (xlO ⁰⁶ ) BrdU+ cells / mm ³ dentate gyrus when evaluated in the assay described in conjunction with Table 1 (i.e., evaluated for pro-neurogenic efficacy / neuroprotection in a standard in vivo hippocampal neurogenesis assay at 10 μΜ concentration in four 12 week old adult male C57/B16 mice. In some embodiments, the compounds or salt (e.g., a pharmaceutically acceptable salt) thereof provide at least about 19 (xlO ⁰⁶ ) BrdU+ cells / mm ³ dentate gyrus when evaluated in the hippocampal neurogenesis assay described in conjunction with Table 1.

In some embodiments, the compounds or salt (e.g., a pharmaceutically acceptable salt) thereof provide from about 18 to about 30 (e.g., 18-27, 19-26, 20-25, 27-30, 27-29) (xlO ^"06 ) BrdU+ cells / mm ³ dentate gyrus when evaluated in the hippocampal neurogenesis assay described in conjunction with Table 1.

In some embodiments, the compounds or salt (e.g., a pharmaceutically acceptable salt) thereof provide from about 18 to about 26 (e.g., 19-26, 20-25) (xlO ⁰⁶ ) BrdU+ cells / mm dentate gyrus when evaluated in the hippocampal neurogenesis assay described in conjunction with Table 1.

In some embodiments, the compounds or salt (e.g., a pharmaceutically acceptable salt) thereof provide from about 27 to about 30 (e.g., 27-29) (xlO ⁰⁶ ) BrdU+ cells / mm dentate gyrus when evaluated in the hippocampal neurogenesis assay described in conjunction with Table 1.

In embodiments, a composition (e.g., a pharmaceutical composition) can include an amount effective to achieve the levels described above.

In embodiments, any compound, composition, or method described herein can also include any one or more of the other features delineated in the detailed description and/or in the claims.

DETAILED DESCRIPTION

Provided herein are embodiments related generally to stimulating neurogenesis (e.g., post-natal neurogenesis, e.g., post-natal hippocampal and/or hypothalamic neurogenesis) and/or promoting the survival of existing neurons by reducing neuronal cell death.

In certain embodiments, the compounds described herein may be neurotrophic. By

"neurotrophic" it is generally meant that the compounds may exert survival-promoting and/or trophic actions on exisiting neuronal cells, and/or stimulate generation of new neurons.

In certain embodiments, the compounds described herein may be pro-neurogenic and/or neuroprotective. By "pro-neurogenic" it is generally meant that the compounds may be useful in promoting, stimulating and/or enhancing neurogenesis, which is the generation of new neurons. By "neuroprotective" it is generally meant that the compounds may protect or prevent neuronal cells from cell death or apoptosis.

The neurotrophic, pro-neurogenic and/or neuroprotective compounds described herein are attractive candidates as therapeutic agents in many clinical conditions and neuropsychiatric or neurodegenerative diseases such as schizophrenia, major depression, bipolar disorder, normal aging, epilepsy, traumatic brain injury, post-traumatic stress disorder, Parkinson's disease, Alzheimer's disease, Down syndrome, spinocerebellar ataxia, amyotrophic lateral sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, abuse of a neuro-active drug, retinal degeneration, spinal cord injury, peripheral nerve injury, physiological weight loss associated with various conditions, as well as cognitive decline associated with normal aging, chemotherapy, and the like. DEFINITIONS

"An effective amount" refers to an amount of a compound that confers a therapeutic effect (e.g., treats, e.g., controls, relieves, ameliorates, alleviates, or slows the progression of; or prevents, e.g., delays the onset of or reduces the risk of developing, a disease, disorder, or condition or symptoms thereof) on the treated subject. The therapeutic effect may be objective (i.e., measurable by some test or marker) or subjecti ve (i.e., subject gives an indication of or feels an effect). An effective amount of the compound described above may range from about 0.01 mg/kg to about 1000 rng/kg, (e.g., from about 0.1 mg/kg to about 100 mg/kg, from about 1 mg/kg to about 100 mg/kg). Effective doses will also vary depending on route of administration, as well as the possibility of co-usage with other agents.

The term "halo" or "halogen" refers to any radical of fluorine, chlorine, bromine or iodine.

In general, and unless otherwise indicated, substituent (radical) prefix names are derived from ihe parent hydride by either (i) replacing the "ane" in. the parent hydride with the suffixes "yl," "diyl," "triyl," "tetrayl," etc.; or (ii) replacing the "e" in the parent hydride with the suffixes "yl," "diyl," "triyl," "tetrayl," etc. (here the atomfs) with the free valence, when specified, is (are) given numbers as low as is consistent with any established numbering of ihe parent hydride). Accepted contracted names, e.g., adamantyl, naphthyl, anthryi, phenanthryl, fury!, pyridyl, isoquinoly!, qumolyl, and piperidyl, and trivial names, e.g., vinyl, alfyl, phenyl, and thienyl are also used herein throughout. Conventional

numbering/lettering systems are also adhered to for substituent numbering and the nomenclature of fused, bicyclic, tricyclic, poiycyelic rings.

The following definitions are used, unless otherwise described. Specific and general values listed below for radicals, substituents, and ranges, are for illustration only; they do not exclude other defined values or other values within defined ranges for the radicals and substituents. Unless otheiwise indicated, alkyi, aikoxy, aikenyl, and the like denote both straight and branched groups.

The term "alkyl" refers to a saturated hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms. For example, Ci -6 alkyi. indicates that the group may have 1 to 6 (inclusive) carbon atoms in it. Any atom can be optionally substituted, e.g., by one or more substituents. Examples of alkyl groups include without limitation methyl, ethyl, n-propyl, isopropyl, and tert- butyl.

As referred to herein, the term "aikoxy" refers to a group of formula— O(alkyi). Aikoxy can be, for example, methoxy (— OCH ₃ ), ethoxy, propoxy, isopropoxy, butoxy, iso-butoxy, sec-butoxy, pentoxy, 2-pentoxy, 3-pentoxy, or hexyloxy. As used herein, the term "hydroxyl," employed alone or in combination with other terms, refers to a group of formula— OH.

The term "alkenyl" refers to a straight or branched hydrocarbon chain containing the indicated number of carbon atoms and having one or more carbon-carbon double bonds. Any atom can be optionally substituted, e.g., by one or more substituents. Alkenyl groups can include, e.g., vinyl, ally], 1- butenyl, and 2-hexenyl. One of the double bond carbons can optionally be the point of attachment of the alkenyl substituent.

The term "alkynyl" refers to a straight or branched hydrocarbon chain containing the indicated number of carbon atoms and having one or more carbon-carbon triple bonds. Alkynyl groups can be optionally substituted, e.g., by one or more substituents. Alkynyl groups can include, e.g., ethynyl, propargy i, and 3 -hexynyl. One of the triple bond carbons can optionally be the point of attachment of the alkynyl substituent.

The term "heterocyclyf" refers to a fully saturated monocyclic, tricyclic, tricyclic or other polycyclic ring system having one or more constituent heteroatom ring atoms independently selected from O, N (it is understood that one or two additional groups may be present to complete the nitrogen valence and/or form a salt), or S. The heteroatom or ring carbon can be the point of attachment of the heterocyclyl substituent to another moiety. Any atom can be optionally substituted, e.g., by one or more substituents. Heterocyclyl groups can include, e.g., tetrahydrofuryl, tetrahydropyranyl, piperidyl

(piperidino), piperazinyl, morpholinyl (morpholino), pyrroiinyl, and pyrroiidinyl. By way of example, the phrase "heterocyclic ring containing from 5-6 ring atoms, wherein 1 -2 of the ring atoms is independently selected from N, NH, N(Ci-Ce alkyl), NC(0)(Ci-C6 alkyl), O, and S; and wherein said heterocyclic ring is optionally substituted with 1-3 independently selected R ^a " would include (but not be limited to) tetrahydrofuryl, tetrahydropyranyl, piperidyl (piperidino), piperazinyl, morpholinyl (morpholino), pyrroiinyl, and pyrroiidinyl.

The term "cycloalkyi" refers to a fully saturated monocyclic, bicyclic, tricyclic, or other polycyclic hydrocarbon groups. Any atom can be optionally substituted, e.g., by one or more substituents. A ring carbon serves as the point of attachment of a cycloalkyi group to another moiety. Cycloalkyi moieties can include, e.g., cyclopropyl, cyelohutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, and norbornyl (bicycle[2.2.1 ]heptyl),

The term "aryl" refers to an aromatic monocyclic, bicyclic (2 fused rings), or tricyclic (3 fused rings), or polycyclic (>3 fused rings) hydrocarbon ring system. One or more ring atoms can be optionally substituted, e.g., by one or more substituents. Aryl moieties include, e.g., phenyl and naphihyl.

The term "heteroaryl" refers to an aromatic monocyclic, bicyclic (2 fused rings), tricyclic (3 fused rings), or polycyclic (>3 fused rings) hydrocarbon groups having one or more heteroatom ring atoms independently selected from O, N (it is understood that one or two additional groups may be present to complete the nitrogen valence and/or form a salt), or S. One or more ring atoms can be optionally substituted, e.g., by one or more substituents. Examples of heteroaryi groups include, but are not limited to, 2H-pyrroly1, 3H-indo!y1, 4H-quinolizinyi, acridinyl, benzo[b]tliienyl, benzothiazolyl, P-carboiinyi, carbazolyl, coumarinyl, chromenyl, cinnolinyl, dibenzo[b,d]furany], furazanyl, furyl, imidazolyi, imidizolyl, indazolyl, indolyl, isobenzofuranyl, isoindolyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthyridinyl, oxazolyl, perimidinyi, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyi, pyranyl, pyrazinyl, pyrazoiyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, quinazolinyl, quinolyl, qumoxal nyl, thiadiazolyf, thianthrenyl, thiazolyl, thienyl, triazolyl, and xanthenyl.

The descriptors "C=Q" or "C(O)" refers to a carbon atom that is doubly bonded to an oxygen atom. Similarly, "S(O)" refers to a sulfur atom that is doubly bonded to an oxygen atom.

The term "carboxyl" refers to a group of formula -C(0)OH. The term "alkoxycarbonyl" refers to a group of formula. The term "carboxyalkyl" refers to a group of formula -(alkyl)-C(0)OH wherein the carboxyl group may be attached to any carbon atom in the alkyl group.

As used herein, the term "cyano," employed alone or in combination with other terms, refers to a group of formula— C , wherein the carbon and nitrogen atoms are bound together by a triple bond. In general, when a definition for a particular variable includes both hydrogen and non-hydrogen (halo, alkyl, aryl, etc.) possibilities, the term "substituent(s) other than hydrogen' refers collectively to the non- hydrogen possibilities for ihai particular variable.

The term "substituent" refers to a group "substituted" on, e.g., an alkyl, haloalkyl, cycloalky], heterocyclyl, heterocycloalkenyl, cycloalkenyf, aryl, or heteroaryi group at any atom of that group, in one aspect, the substituent(s) on a group are independently any one single, or any combination of two or more of the permissible atoms or groups of atoms delineated for that substituent. In another aspect, a substituent may itself be substituted with any one of the above substituents. Further, as used herein, the phrase "optionally substituted" means utisubstituted (e.g., substituted with an H) or substituted. As used herein, the term "substituted" means that a hydrogen atom is removed and replaced by a substituent. It is understood that substitution at a given atom is limited by valency.

COMPOUNDS

Compounds of formula (I)-(V) as defined herein, or any combinations of the definitions of the various groups, are encompassed by the presently disclosed embodiments. Various compounds will be further described in the following examples. It should be understood that these examples are for illustrative purposes only and are not to be construed as limiting the presently disclosed embodiments in any manner. P7C3-S132: l-(10,ll-dihydro-5H-dibenzo[b,f|azepin-5-yl)-3-(lH-indol-l-y l)propan-2-ol.

Step 1 : Synthesis of 5-(oxiran-2-ylm dro-5H-dibenzo[b,f]azepine.

n-BuLi (25.6 mL, 40.9 mmol) was added to a stirred solution of iminodibenzyl (4.00 g,

20.2 mmol) in dry THF (24 mL) at -78 °C and under atmosphere of N ₂ . The mixture was allowed to stir at the same temperature for 20 min and then epibromohydrin (8.48 mL, 102 mmol) was added. The resulting mixture was stirred overnight allowing the reaction to warm up to room temperature. Upon completion, the reaction was partitioned between EtOAc and H ₂ 0. The aqueous layer was washed with EtOAc. The combined organic extracts were washed with brine, dried over MgSO/t, filtered, and concentrated in vacuo. The crude residue was purified by chromatography (S1O ₂ , 98:2 Hexanes/EtOAc) to afford the desired product as colorless solid (3.00 g, 59%). The spectroscopic data were in full agreement with those reported in the literature (Levy, O.; Erez, M.; Varon, D.; Keinan, E. Bioorg. Med. Chem. Lett. 2001, 11, 2921-2926).

Step 2: 1-(10, 1 l-dihydro-5H-dibenzo[b,f]azepin-5-yl)-3-(lH-indol-l-yl)propa n-2-ol. (P7C3-

S I 32)

Indole (36.0 mg, 0.30 mmol) was added to a suspension of NaH (20.0 mg, 0.48 mmol) in of DMF (5 mL) at 0 °C. The mixture was allowed to stir at 0 °C for 10 min and then at room temperature for 30 min. 5-(oxiran-2-ylmethyl)-10,l l-dihydro-5H-dibenzo[b,f]azepine (75.0 mg, 0.30 mmol) was then added and the reaction mixture was stirred overnight at room temperature. Upon completion, the reaction was partitioned between EtOAc and H ₂ 0. The aqueous layer was washed EtOAc. The combined organic extracts were washed with brine, dried over MgS0 ₄ , filtered, and concentrated in vacuum. The crude residue was purified by chromatography (S1O ₂ , 9: 1 Hexanes/EtOAc) to afford the desired product as colorless solid (90.3 mg, 82%).

lU NMR (CDCI ₃ , 500 MHz) δ 7.60 (d, 1H, J= 7.2 Hz), 7.18-7.05 (m, 7H), 7.05-6.95 (m, 5H), 6.47 (d, 1H, J= 2.8 Hz), 4.36 (dd, 1H, J= 3.2, 14.4 Hz), 4.20 (m _c , 1H), 4.05 (dd, 1H, J= 7.5, 14.5 Hz), 3.80 (d, 2H, J= 6.5 Hz), 3.27-3.18 (m, 4H), 2.14 (br s, 1H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 147.9, 136.4, 134.3, 130.4, 128.9, 128.8, 127.0, 123.6, 121.8, 121.2, 1 19.9, 119.7, 109.5, 101.8, 68.3, 54.4, 50.6, 32.3. MS (ESI) m/z: 369.0 [M+H] ⁺ ([M+H] ⁺ for C ₂₅ H ₂₅ N ₂ 0 requires 369.1). [b,f|azepin-5-yl)propan-2-ol.

Following the same procedure as for P7C3-S132, P7C3-S133 was prepared from 5-(oxiran-2- ylmethyl)-10,l l-dihydro-5H-dibenzo[b,f]azepine (75.0 mg, 0.30 mmol) and 9H-carbazole (51 mg, 0.3 mmol) with NaH (20.0 mg, 0.48 mmol) in DMF (5 mL) and isolated as a colorless solid (101.4 mg, 81%).

¾ NMR (CDC1 ₃ , 500 MHz) δ 8.10 (d, 2H, J= 7.7 Hz), 7.40 (m _c , 2H), 7.29-7.13 (m, 8H), 7.10- 7.01 (m, 4H), 4.51 (dd, 1H, J= 2.7, 14.7 Hz), 4.43 (m _c , 1H), 4.35 (dd, 1H, J= 7.9, 14.6 Hz), 4.01 (dd, 1H, J= 6.5, 12.7 MHz), 3.90 (dd, 1H, J= 6.6, 12.7 MHz), 3.33-3.23 (m, 4H), 2.14 (br s, 1H). ¹³ C NMR (CDCI ₃ , 126 MHz) δ 147.9, 141.0, 134.3, 130.4, 127.0, 126.0, 123.6, 123.1, 120.4, 1 19.9, 1 19.4, 109.1, 68.2, 54.6, 47.7, 32.3. MS (ESI) m/z: 419.0 [M+H] ⁺ ([M+H] ⁺ for C ₂ 9H ₂₇ N ₂ 0 requires 419.2). P7C3-S134: l-(10,ll-dihydro-5H-dibe (phenylthio)propan-2-ol.

Benzenethiol (34 μΕ, 0.33 mmol) was added to a solution of 5-(oxiran-2-ylmethyl)-10, l 1- dihydro-5H-dibenzo[b,f]azepine (75.0 mg, 0.30 mmol) in MeOH (5.6 mL) at room temperature. The reaction mixture was heated to 80 °C and stirred overnight at the same temperature. The reaction was monitored by LC/MS for the consumption of starting material. The reaction was cooled to room temperature, diluted with EtOAc and washed with H ₂ 0 and brine. The organic layer was dried over Na ₂ S0 ₄ , filtered and condensed. The crude residue was purified by chromatography (Si0 ₂ , 9: 1

Hexanes/EtOAc) to afford the desired product (66.0 mg, 61%).

^ NMR CDCls, 500 MHz) δ 7.19-7.05 (m, 1 1H), 6.96 (m _c , 2H), 3.97 (m _c , 1H), 3.89 (d, 1H, J= 6.3 Hz), 3.26 (dd, 2H, J= 4.1, 13.9 Hz), 3.18 (s, 4H), 2.96 (dd, 1H, J= 7.3, 13.9 Hz). ¹³ C NMR

(CDCI ₃ , 126 MHz) δ 147.9, 134.2, 130.2, 129.1, 126.8, 126.2, 123.3, 1 19.9, 66.9, 55.7, 39.2, 32.3. MS (ESI) m/z: 361.9 [M+H] ⁺ ([M+H] ⁺ for C ₂₃ H ₂₄ NOS requires 362.1). P7C3-S135: l-(10,ll-dihydro-5H-dibenzo[b,f|azepin-5-yl)-3-phenoxypropan -2-ol.

To a stirred solution of iminodibenzyl (75 mg, 0.38 mmol) in dry THF (1.5 mL) was added n- BuLi (0.3 mL, 0.68 mmol, 2.5 M in hexanes) at -78 °C and the resulting mixture was stirred for 30 min. 2-(phenoxymethyl)oxirane (0.13 mL, 0.95 mL) was added and the reaction was allowed to warm slowly to ambient temperature and stirred overnight. Upon completion, the reaction was quenched with saturated aqueous NH ₄ C1 and the mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried over Na ₂ S0 ₄ , filtered, and concentrated. The crude residue was purified by

chromatography (Si0 ₂ , 9: 1 Hexanes/EtOAc) to afford the desired product (92.0 mg, 70%).

H NMR (CDCI ₃ , 500 MHz) δ 7.29 (t, 2H, J= 8.0 Hz), 7.20-7.1 1 (m, 6H), 7.02-6.95 (m, 3H),

6.88 (d, 2H, J= 8.5 Hz), 4.23 (m _c , 1H), 4.1 1 (dd, 2H, J= 3.7, 9.6 Hz), 4.06-3.95 (m, 2H), 3.21 (s, 4H). ¹³ C NMR (CDCI ₃ , 126 MHz) δ 158.6, 148.0, 134.4, 130.2, 129.6, 126.8, 123.3, 121.2, 119.9, 1 14.6, 70.3, 67.4, 53.7, 32.2. MS (ESI) m/z: 346.0 [M+H] ⁺ ([M+H] ⁺ for C ₂₃ H ₂₄ N0 ₂ requires 346.1).

P7C3-S139: l-(10,ll-dihydro-5H-dibe -(dimethylamino)propan-2-ol.

5-(Oxiran-2-ylmethyl)-10,l l-dihydro-5H-dibenzo[b,f]azepine (75 mg, 0.3 mmol) was added to a 25 mL scintillation vial followed by Μβ ₂ ΝΗΉ01 (37.0 mg, 0.45 mmol) and K ₂ C0 ₃ (125 mg, 0.9 mmol). The vial was heated to reflux for 2 h. Upon completion the reaction was cooled to room temperature, the solids were filtered off and the solvent was evaporated in vacuum. The crude residue was purified by chromatography (Si0 ₂ , 98:2 CH ₂ Cl ₂ /MeOH + 1% NH ₄ OH) to afford the desired product as a white solid (76.0 mg, 86%).

'H NMR (CDCI ₃ , 500 MHz) δ 7.10-7.00 (m, 6H), 6.87 (m _c , 2H), 3.86-3.75 (m, 2H), 3.73 (brs, 1H), 3.58 (dd, 1H, J= 6.2, 12.2 Hz), 3.1 1 (s, 4H), 2.41-2.28 (m, 2H), 2.09 (s, 6H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.0, 134.1, 129.9, 126.5, 122.8, 1 19.8, 65.3, 64.4, 55.3, 45.6, 32.1. MS (ESI) m/z: 297.0 [M+H] ⁺ ([M+H] ⁺ for Ci ₉ H ₂₅ N ₂ 0 requires 297.1). P7C3-S140: l-amino-3-(10,ll-dihydro-5 -dibenzo[b,f|azepin-5-yl)propan-2-ol.

5-(Oxiran-2-ylmethyl)-10,l l-dihydro-5H-dibenzo[b,f]azepine (262 mg, 1.04 mmol) was added to a 25 mL scintillation vial followed by NH ₃ -MeOH (7N, 6.0 mL). The vial was heated to reflux for 12 h. Upon completion the reaction was cooled to room temperature and concentrated under reduced pressure to remove the remaining methanol. The crude residue was purified by chromatography (Si0 ₂ , 98:2 CH ₂ Cl ₂ /MeOH + 1% NH ₄ OH) to afford the desired product as an amorphous yellow foam (76.0 mg, 86%).

¾ NMR (CDC1 ₃ , 500 MHz) δ 7.10-7.02 (m, 6H), 6.88 (m _c , 2H), 3.76 (dd, 1H, J= 6.0, 12.1 Hz), 3.68 (brs, 1H), 3.63 (dd, 1H, J= 6.2, 12.1 Hz), 3.31 (brs, 2H), 3.1 1 (s, 4H), 2.78 (d, 1H, J= 13.1 Hz,), 2.55 (dd, 1H, J= 7.3, 13.1 Hz). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.1, 134.2, 130.1, 126.7, 123.1, 120.0, 67.3, 67.2, 55.1, 53.6, 53.5, 32.2. MS (ESI) m/r. 269.0 [M+H] ⁺ ([M+H] ⁺ for Ci ₇ H ₂₁ N ₂ 0 requires 269.1).

P7C3-S143 : 1-(10,1 l-dihydro-5H-dibe -(methylamino)propan-2-ol.

Following the same procedure as for P7C3-S139, P7C3-S143 was prepared from 5-(oxiran-2- ylmethyl)-10, l l-dihydro-5H-dibenzo[b,f]azepine (75.0 mg, 0.30 mmol) and MeNH ₂ ^' HCl (30.4 mg, 0.45 mmol) with K ₂ CC>3 (125 mg, 0.9 mmol) and isolated as a white solid (57.0 mg, 68%).

'H NMR (CDCI ₃ , 500 MHz) δ 7.21-7.10 (m, 6H), 6.98 (m _c , 2H), 3.98 (brs, 1H), 3.91 (dd, 1H, J = 5.1, 12.9 Hz), 3.84 (dd, 1H, J= 7.2, 12.9 Hz), 3.53 (dd, 1H, J= 3.4, 9.6 Hz), 3.43 (dd, 1H, J= 5.7, 9.6 Hz), 3.37 (s, 3H), 3.20 (s, 4H), 2.51 (d, 1H, J= 3.0 Hz).

¹³ C NMR (CDCI ₃ , 126 MHz) δ 148.1, 134.3, 130.1, 126.7, 123.1, 120.0, 75.0, 67.6, 59.4, 53.7,

32.2.

MS (ESI) m/r. 284.0 [M+H] ⁺ ([M+H] ⁺ for Ci ₈ H ₂₃ N ₂ 0 requires 283.1).

P7C3-S144: l-(10,ll-dihydro-5H-dibenzo[b,f|azepin-5-yl)-3-(isopropylami no)propan-2-ol.

5-(Oxiran-2-ylmethyl)-10,l l-dihydro-5H-dibenzo[b,f]azepine (100 mg, 0.4 mmol) was added to a 25 mL scintillation vial followed by isopropanol (2 mL) and isopropylamine (2 mL, 23.3 mmol). The vial was heated to reflux for 12 h. Upon completion the reaction was cooled to room temperature, and the solvent was evaporated in vacuum. The crude residue was recrystallized (Hexanes/EtOAc) to give the desired product as a white solid (74.0 mg, 60%).

lU NMR (CDC1 ₃ , 500 MHz) δ 7.16-7.08 (m, 6H), 6.94 (m _c , 2H), 3.86 (dd, 1H, J= 6.6, 1 1.9 Hz), 3.81 (brs, lH), 3.74 (dd, 1H, J= 5.0, 1 1.9 Hz), 3.18 (s, 4H), 2.82 (dd, 1H, J= 2.9, 11.9 Hz), 2.73 (m, 1H), 2.54 (dd, 1H, J= 7.5, 1 1.9 Hz), 2.14 (brs, 1H), 1.01 (d, 6H, J= 6.2 Hz,). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.2, 134.3, 130.1, 126.7, 123.1, 120.1, 67.2, 55.3, 50.1, 49.0, 32.3, 23.2, 23.1. MS (ESI) m/z: 31 1.0 [M+H] ⁺ ([M+H] ⁺ for C ₂ oH ₂₇ N ₂ 0 requires 31 1.2).

P7C3-S145: l-(tert-butylamino)-3-(10,l -dihydro-5H-dibenzo[b,f|azepin-5-yl)propan-2-ol.

5-(Oxiran-2-ylmethyl)- 10, 1 1 -dihydro-5H-dibenzo[b,f]azepine (100 mg, 0.4 mmol) was added to a 25 mL scintillation vial followed by tert-butanol (1 mL) and tert-butylamine (3 mL, 28.5 mmol). The vial was heated to reflux for 12 h. Upon completion the reaction was cooled to room temperature, and the solvent was evaporated in vacuum. The crude residue was purified by chromatography (Si0 ₂ , 98:2 CH ₂ Cl ₂ /MeOH + 1% NH ₄ OH) to afford the desired product as a white solid (123 mg, 95%).

'H NMR (CDCI ₃ , 500 MHz) δ 7.18-7.07 (m, 6H), 6.95 (m _c , 2H), 3.94 (dd, 1H, J= 6.0, 12.6 Hz),

3.76 (brs, 1H), 3.69 (dd, 1H, J= 6.5, 12.6 Hz), 3.19 (s, 4H), 2.79 (dd, 1H, J= 2.7, 1 1.7 Hz), 2.50 (dd, 1H, J= 7.9, 1 1.7 Hz), 1.05 (s, 9H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.3, 134.3, 130.0, 126.7, 123.0, 120.1, 67.5, 55.3, 50.3, 46.2, 32.3, 29.2.

MS (ESI) m/z: 325.0 [M+H] ⁺ ([M+H] ⁺ for C ₂ iH ₂₉ N ₂ 0 requires 325.2).

P7C3-S148: 3-(10,ll-dihydro-5H-dibenzo[b,f|azepin-5-yl)-2-fluoro-N,N-di methylpropan-l-amine.

An oven dried 20 mL scintillation vial containing 1-(10, 1 l-dihydro-5H-dibenzo[b,f]azepin-5-yl)- 3-(dimethylamino)propan-2-ol (47.0 mg, 0.16 mmol) was purged with N ₂ and charged with anhydrous CH ₂ CI ₂ (9.0 mL, 0.018 M). The sealed vial was cooled in a dry ice acetone bath before the dropwise addition of morpholinosulfur trifluoride (morpho-DAST, 39 0.32 mmol). The reaction temperature was maintained at -78 °C for an hour and then slowly warmed to room temperature and stirred overnight. The reaction was quenched with saturated NaHCC>3 solution and diluted with CH ₂ CI ₂ and extracted three times. The combined organics were dried over Na ₂ S0 ₄ , filtered and condensed. The crude residue was purified by chromatography (S1O ₂ , 8:2 Hexanes/EtOAc) to afford the desired product (12.3 mg, 26%).

¾ NMR (CDCI ₃ , 500 MHz) δ 7.187-7.08 (m, 6H), 6.94 (m _c , 2H), 4.81-4.64 (m, 1H), 4.00 (d, 1H,

J= 6.0 Hz), 3.97 (t, 1H, J= 5.6 Hz), 3.17 (s, 4H), 2.64-2.56 (m, 1H), 2.56-2.52 (m, 1H), 2.23 (s, 6H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 147.9, 134.7, 130.1, 126.7, 123.1, 120.2, 90.5, 88.7, 62.1 (d, J= 20.6 Hz), 53.9 (d, J= 25.8 Hz), 46.3, 32.1. MS (ESI) m/z: 299.0 [M+H] ⁺ ([M+H] ⁺ for C ₁₉ H ₂₄ FN ₂ requires 299.1). P7C3-S149: l-(10,ll-dihydro-5H-dibe -fluoro-N,N-dimethylpropan-2-amine.

1-(10, 1 l-dihydro-5H-dibenzo[b,f]azepin-5-yl)-3-fluoro-N,N-dimethylp ropan-2-amine was obtained as main product in the synthesis of (P7C3-S148) (28.5 mg, 60%).

'H NMR (CDCI ₃ , 500 MHz) δ 7.17-7.08 (m, 6H), 6.95 (m _c , 2H), 4.61 (dd, 2H, J= 3.7, 47.8 Hz), 4.09 (dt, 1H, J= 3.3, 12.5 Hz), 3.62 (m, lH), 3.16 (s, 4H), 2.94 (ddd, 1H, J= 4.3, 9.4, 25.6 Hz), 2.42 (s, 6H). ¹³ C NMR (CDCI ₃ , 126 MHz) δ 148.3, 134.4, 130.2, 126.7, 123.0, 1 19.8, 61.0, 60.9, 48.4, 42.0, 32.2. MS (ESI) m/z: 299.0 [M+H] ⁺ ([M+H] ⁺ for C ₁₉ H ₂₄ FN ₂ requires 299.1).

P7C3-S152: 3-(10,ll-dihydro-5H-dibenzo[b,f|azepin-5-yl)-2-fluoro-N-meth ylpropan-l-amine. Step 1. Synthesis ofN-(3-(10,ll-dihydro-5H-dibenzo[b,f]azepin-5-yl)-2-hydroxyp ropyl)-N-methyl-4- nitrobenzenesulfonamide

A heterogeneous mixture of N-methyl-4-nitrobenzenesulfonamide (95.0 mg, 0.44 mmol) (synthesized following a reported procedure: Harshani R. L.; Kazi, A; Ge, Y; Guida, W. C; Sebti, S.; Luo, Y.; Kendig, R.; Jain, S.; Daniel, K.; Santiago, D., Bioorg. Med. Chem. 2010, 18, 5576-5592) in toluene (3.4 mL, 0.13 M) under a N ₂ atmosphere was cooled in a dry ice/acetone bath before dropwise addition of «-BuLi (0.240 mL of 2.5 M in hexanes, 0.60 mmol). The reaction was stirred at -78 °C for 20 minutes before addition of 5-(oxiran-2-ylmethyl)- 10,l l-dihydro-5H-dibenzo[b,f]azepine (100 mg, 0.4 mmol). The heterogeneous mixture was stirred at room temperature for 5 min before heating at 100 °C for 72 h. The cooled reaction was diluted with EtOAc and washed 3x5% acetic acid solution, followed by a brine wash. The organic layer was dried over Na ₂ S0 ₄ , filtered and condensed. The crude residue was purified by chromatography (S1O ₂ , 7:3 Hexanes/EtOAc) to afford the desired product (45.0 mg, 25%). lU NMR (CDCI ₃ , 500 MHz) δ 8.32 (d, 2H, J= 8.6 Hz), 7.90 (d, 2H, J= 8.6 Hz), 7.20-7.07 (m, 6H), 6.98 (m _c , 2H), 3.99-3.91 (m, 2H), 3.75 (m _c , 1H), 3.34-3.27 (m, 1H), 3.16 (s, 4H), 2.85 (s, 3H). ¹³ C NMR (CDCI ₃ , 126 MHz) δ 147.8, 134.2, 130.3, 128.6, 126.9, 124.5, 123.6, 119.9, 63.3, 54.5, 54.3, 37.0, 32.2. MS (ESI) m/z: 467.9 [M+H] ⁺ ([M+H] ⁺ for C ₂ 4H ₂₆ N ₃ 0 ₅ S requires 468.1).

Step 2. Synthesis of N-(3-(l 0, 1 l-dihydro-5H-dibenzo[b,f] azepin-5-yl)-2-fluoropropyl)-N-methyl-4- nitrobenzenesulfonamide

This intermediate was prepared analogously to P7C3-S148. The crude product was carried forward without further purification.

lU NMR (CDCI ₃ , 500 MHz) δ 8.24 (d, 2H, J= 8.8 Hz), 7.77 (d, 2H, J= 8.8 Hz), 7.20-7.05 (m,

6H), 7.01 (m _c , 2H), 4.76-4.55 (m, 1H), 4.10 (td, 1H, J= 5.8, 13.4 Hz), 3.87 (td, 1H, J= 6.6, 13.9,

14.8 Hz), 3.78-3.60 (m, 2H), 3.20 (s, 4H), 2.87 (s, 3H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 147.6, 134.8, 130.4, 128.4, 126.8, 124.5, 123.6, 1 19.9, 91.0, 89.2, 67.0, 52.7 (dd, J= 23.7, 32.1 Hz), 44.4, 36.5, 32.0.

MS (ESI) m/z: 469.9 [M+H] ⁺ ([M+H] ⁺ for Cz-OfeFNsC S requires 470.1). Step 3. Synthesis of 3-(10, l 1 -dihydro-5H-dibenzo [b,J] azepin-5-yl)-2-fluoro-N-methylpropan-l -amine (P7C3-S152).

To a vial containing N-(3-(10, l l -dihydro-5H-dibenzo[b,f azepin-5-yl)-2-fluoropropyl)-N-methyl- 4-nitrobenzenesulfonamide (53.2 mg, 0.1 13 mmol) was added lithium hydroxide (12.2 mg, 0.510 mmol), DMF (2.0 mL, 0.06 M) and mercaptoacetic acid (16.0 0.227 mmol). After stirring at room

temperature for 1 h the reaction mixture was diluted with EtOAc and washed sequentially with H ₂ 0, saturated aqueous NaHC0 ₃ , H ₂ 0 (3 x) and brine. The organic layer was dried over Na ₂ S0 ₄ , filtered and condensed. The crude residue was purified by chromatography (Si0 ₂ , 98:2 CH ₂ Cl ₂ /MeOH + 1% Et ₃ N) to afford the desired product (14.5 mg, 47%).

¾ NMR (CDC1 ₃ , 500 MHz) δ 7.09-6.95 (m, 6H), 6.86 (m _c , 2H), 4.77-4.55 (m, 1H), 3.97 (td, 1H, J= 6.6, 13.8 Hz), 3.85 (m _c , 1H), 3.07 (s, 4H), 2.82-2.75 (m, 1H), 2.74-2.68 (m, 1H), 2.31 (s, 3H). ¹³ C NMR (CDCI ₃ , 126 MHz) δ 147.6, 134.5, 130.0, 126.6, 123.2, 1 19.9, 90.4, 88.7, 53.3 (dd, J= 22.7, 46.9 Hz), 49.0 (dp, J= 21.4, 42.9 Hz), 35.6, 31.9.

MS (ESI) m/z: 285.0 [M+H] ⁺ ([M+H] ⁺ for Ci ₈ H ₂₂ FN ₂ requires 285.1).

P7C3-S158: l-(10,ll-dihydro-5H-di -methoxyphenyl)amino)propan-2-ol.

Following the same procedure as for P7C3-S135, P7C3-S158 was prepared from iminodibenzyl (68.2 g, 0.35 mmol) and 3-methoxy-N-(oxiran-2-ylmethyl)aniline (75.1 mg, 0.42 mmol) with «-BuLi

(0.167 mL of 2.5 M in hexanes, 0.42 mmol) in dry THF (1 mL) and isolated after chromatography (Si0 ₂ , 7:3 Hexanes/EtOAc) (10.5 mg, 8%).

'H NMR (CDCI ₃ , 400 MHz) δ 7.17-7.09 (m, 6H), 7.04 (m _c , 2H), 7.00-6.94 (m, 2H), 6.30 (dd, 1H, J= 2.3, 8.2 Hz), 6.22-6.15 (m, 2H), 4.07 (m _c , 1H), 3.94 (dd, 1H, J= 4.9, 13.0 Hz), 3.82 (dd, 1H, J= 8.0, 13.0 Hz), 3.74 (s, 3H), 3.38 (dd, 1H, J= 3.4, 12.8 Hz), 3.20 (s, 4H), 3.12 (dd, 1H, J= 7.0, 12.8 Hz). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.0, 134.3, 130.3, 130.2, 126.8, 123.5, 1 19.9, 106.6, 103.7, 99.5, 67.1 , 55.2, 54.9, 48.2, 32.3.

MS (ESI) m/z: 375.0 [M+H] ⁺ ([M+H] ⁺ for C ₂₄ H ₂₇ N ₂ 0 ₂ requires 375.2). P7C3-S162: 3 6-dibromo-9H-carbazole.

This analog was purchased from SigmaAldrich

P7C3-S163: 3 6-dibromo-9-methyl-9H-carbazole

The title compound was prepared from P7C3-S 162 by methylation with NaH and methyl iodide. The ^l U NMR data was consistent with that reported in Eur. J. Med. Chem. 1997 (32) 781.

P7C3-S164: ethyl 2-(3,6-dibromo-9H-carbazol-9-yl)acetate

Sodium Hydride was added to a stirred solution of 3,6-dibromocarbazole (250 mg, 0.77 mmol) in DMF (4 ml). The solution was stirred for 30 minutes before the dropwise addition of ethyl chloroacetate. After 12 hours water was added and a fine white precipitate formed which was filtered and rinsed with water and hexanes to afford the desired ethyl ester in 93% yield.

¾ NMR (500 MHz, CDC1 ₃ ) δ 8.15 (s, 2H), 7.56 (d, J= 8.6 Hz, 2H), 7.21 (d, J= 8.5 Hz, 2H), 4.94 (s, 2H), 4.20 (q, J= 6.3 Hz, 2H), 1.26 - 1.18 (m, 3H). ESI m/z: 409.7 ([M+H] ⁺ , Ci ₆ H ₁₃ Br ₂ N0 ₂ requires 409.9)

P7C3-S165: 2-(3,6-dibromo-9H-carbazol-9-yl)acetic acid

Ethyl 2-(3,6-dibromo-9H-carbazol-9-yl)acetate (50 mg, 0.12 mmol) was dissolved in 0.6 ml of THF. To this stirred solution was added 0.4 ml of methanol, 0.2 ml of water, and lithium hydroxide (14.5 mg, 0.6 mmol). After 1 hour all starting material had been consumed. The solution was acidified with IN HC1. Upon reaching a pH of about 4 precipitate had formed which was collected and rinsed with fresh water to afford the desired acid in 95% yield.

^! H NMR (500 MHz, Acetone-i/ ₆ ) δ 8.41 (s, 2H), 7.62 (dt, J= 8.6, 1.7 Hz, 2H), 7.58 (dd, J= 8.7, 1.5 Hz, 2H), 5.31 (d, J= 1.6 Hz, 2H). ESI m/z: 381.7 ([M+H] ⁺ , Ci ₄ H ₉ Br ₂ N0 ₂ requires 381.9)

P7C3-S169: l-(3,6-dibromo-9H-carbazol-9-yl)-2-methylpropan-2-ol

A flask was charged with ethyl 2-(3,6-dibromo-9H-carbazol-9-yl)acetate (100 mg, 0.243 mmol) and purged with nitrogen gas. Anhydrous THF (2ml) was added and the solution was cooled to -78 °C in a dry ice/acetone bath. Methyl magnesium bromide (0.19 mL of a 3M ether solution) was added drop wise. The reaction was warmed to room temperature and stirred overnight. Upon completion the reaction was cooled to 0 °C and NH ₄ C1 (sat.) was added. The mixture was extracted with ethyl acetate, washed with water, brine and dried over magnesium sulfate. The crude mixture was purified on S1O ₂ (10% EtOAc/hexanes. Isolated yield was 69 %.

'H NMR (500 MHz, CDCI ₃ ) δ 8.14 (s, 2H), 7.55 (d, J= 8.7 Hz, 2H), 7.41 (d, J= 8.7 Hz, 2H), 4.24 (s, 2H), 1.35 (s, 6H). ESI m/z: 439.95 ([M+HCOO] ^" , Ci ₆ H ₁₅ Br ₂ NO requires 394.95 )

P7C3-S170 : 1 ,3-bis(l 0,1 l-dihydro-5H-dibenzo [b,f] azepin-5-yl)propan-2-ol.

P7C3-S 170 was obtained as a by-product in the synthesis of 5-(oxiran-2-ylmethyl)- 10, l 1 - dihydro-5H-dibenzo[b,f]azepine and isolated as a white solid (74.7 mg, 33%).

lU NMR (CDC1 ₃ , 500 MHz) δ 7.14 (d, 4H, J= 7.3 Hz), 7.03 (d, 4H, J = 7.1 Hz), 6.99-6.84 (m, 8H), 4.10 (m _c , 1H), 3.97 (dd, 2H, J= 5.3, 12.9 Hz), 3.79 (dd, 2H, J= 7.2, 12.9 Hz), 3.24 (m _c , 8H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 148.0, 134.1 , 130.1 , 126.7, 123.1 , 1 19.7, 65.4, 55.2, 32.3. MS (ESI) m/z: 447.0 [M+H] ⁺ ([M+H] ⁺ for C ₃ iH ₃ iN ₂ 0 requires 447.2).

P7C3-S171: 2-(3,6-dibromo-9H-carbazol-9-yl)ethanol

Ethyl 2-(3,6-dibromo-9H-carbazol-9-yl)acetate (50 mg, 0.12 mmol) was dissolved in 1 ml of THF. L1BH ₄ (5.3 mg, 0.24 mmol) was added, and the mixture was heated to 60 °C for 45 minutes. The reaction was cooled to room temperature and 10% NaHC0 ₃ was added. This material was extracted with EtOAc, washed with IN HCl, H ₂ 0, and brine. The crude material did not require further purification.

'H NMR (500 MHz, CDC1 ₃ ) δ 8.15 (s, 2H), 7.56 (d, J = 8.7 Hz, 2H), 7.35 (d, J= 8.7 Hz, 2H),

4.44 (t, J= 4.8 Hz, 2H), 4.05 (t, J= 4.8 Hz, 2H).ESI m/z: 367.7 ([M+H] ⁺ , C ₁₄ H _u Br ₂ NO requires 367.92)

P7C3-S185: l-(naphthalen- 1 -ylamino)-3-(2-phenyl- lH-indol- 1 -yl)propan-2-ol

The title compound was synthesized according to Asso et al., ChemMedChem, 2008, (3) 1530. P7C3-S189: 9- 3-azido-2-fluoropropyl)-3,6-dibromo-9H-carbazole

The title compound was prepared by opening 3,6-dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole with NaN3 in ethanol, followed by fluorination according to Representative Procedure 4.

MS (ESI) m/z: 468.6, [M+formate]-, Ci ₅ H _u Br ₂ FN ₄ requires 423.9

P7C3-S193: melatonin

This compound was purchased from SigmaAldrich.

P7C3-S199: vinpocetine

This compound was purchased from SigmaAldrich

P7C3-S200: PK 1 1195

This compound was purchased from SigmaAldrich

P7C3-S201: N,N-Dihexyl-2-(4-fluorophenyl)indole-3-acetamide, also known as FGIN-1-27.

This compound was purchased from SigmaAldrich.

P7C3-S203: 4'-chlorodiazepam

This compound was purchased from SigmaAldrich.

P7C3-S207: 5-bromo-DL-tryptophan.

This compound was purchased from SigmaAldrich.

P7C3-S206: 6-bromo-9H-pyrido[3,4-b]indole-3-carboxylic acid

Ethyl 6-bromo-9H-pyrido[3,4-b]indole-3-carboxylate was suspended in 10% NaOH _(aq.) and heated to reflux for 3 hours. Upon completion the reaction was cooled to room temperature and acidified with ice cold HC1 ( _CO nc.)- The temperature was maintained at 0 °C and stirred for 1 hour. The precipitate was filtered, rinsed with water, and dried under vacuum to afford the desired compound in 91% yield.

^ NMR ^OO MHz, DMSO-i/ ₆ ) δ 12.92 (s, 1H), 9.30 (s, 1H), 9.18 (s, 1H), 8.90 (s, 1H), 7.87 (d, J = 8.7 Hz, 1H), 7.80 (d, J= 8.8 Hz, 1H). ESI m/z: 290.8 ([M+H] ⁺ , Ci ₂ H ₇ BrN ₂ 0 ₂ requires 290.97)

P7C3-S209: Synthesis of 3-bromo-6-methoxy-9H-carbazole

e

3-Methoxy-9H-carbazole (Bedford, R. B.; Betham, M. J. Org. Chem. 2006, 71, 9403-9410)

(0.029 g, 0.147 mmol) was dissolved in dry DMF (0.28 mL) and NBS (0.026 g, 0.147 mmol) was added to the solution. The reaction mixture was stirred at room temperature for 2 h under absence of light. The solution was poured into water (2 mL), filtered and washed with water. The title compound was isolated as a grey solid (0.033 g, 82%).

'H NMR (CDCI ₃ , 400 MHz) δ 8.13 (s, 1H), 7.91 (brs, 1H), 7.50-7.43 (m, 2H), 7.30 (d, 1H, J=

8.7 Hz), 7.25 (d, 1H, J= 5.6 Hz), 7.08 (d, 1H, J= 8.7 Hz), 3.91 (s, 3H). MS (ESI) m/z 276.9 [M+H] ⁺ ([M+H] ⁺ , CisHnBrNO requires 276.0).

P7C3-S210: 2-(10,ll-dihydro-5H-dibenzo cetic acid.

P7C3-S210 was prepared analogously to P7C3-S 165 (276 mg, 85%).

'H NMR (CDCI ₃ , 500 MHz) δ 7.15-7.09 (m, 4H), 7.03 (d, 2H, J= 7.9 Hz), 6.96 (t, 2H,

J= 7.3 Hz), 4.58 (s, 2H), 3.21 (s, 4H). ¹³ C NMR (CDC1 ₃ , 126 MHz) δ 175.5, 147.5, 134.5, 130.2, 126. 123.4, 1 19.6, 54.6, 32.6. MS (ESI) m/z: 254.0 [M+H] ⁺ ([M+H] ⁺ for Ci ₆ H ₁₆ N0 ₂ requires 254.1).

P7C3-S211: 2-(3,6-dibromo-9H-carbazol-9-yl)propanoic acid

Step 1: ethyl 2-(3,6-dibromo-9H-carbazol-9-yl)propanoate

Synthesized analogously to P7C3-S 164.

^ NMR ^OO MHz, CDCI ₃ ) δ 8.15 (d, J= 1.8 Hz, 2H), 7.54 (dd, J= 8.7, 1.9 Hz, 2H), 7.26 (d, J = 8.7 Hz, 2H), 5.31 (q, J= 7.3 Hz, 1H), 4.17 (q, J= 7.1 Hz, 2H), 1.80 (d, J= 7.3 Hz, 3H), 1.12 (t, J= 7.1 Hz, 3H). ESI m/z: 423.7 ([M+H] ⁺ , Ci ₇ H ₁₅ Br ₂ N0 ₂ requires 423.95)

Step 2: P7C3-S21 1 : 2-(3,6-dibromo-9H-carbazol-9-yl)propanoic acid

Synthesized analogously to P7C3-S 165.

^! H NMR (400 MHz, CDCL ₃ ) δ 8.16 (d, J= 1.8 Hz, 2H), 7.55 (dd, J= 8.7, 1.8 Hz, 2H), 7.27 (s, 2H), 5.39 (dd, J= 14.7, 7.3 Hz, 1H), 1.85 (d, J= 7.3 Hz, 3H). ESI m/z: 395.7 ([M+H] ⁺ , C ₁₅ H ₂₁ Br ₂ N0 ₂ requires 395.92)

P7C3-S212: iminodibenzyl

This compound was purchased from SigmaAldrich.

P7C3-S216: 6-bromo-9H-carbazole-3-carbonitrile

Step 1 : 9-H-carbazole-3-carbonitrile

N

3-bromo-9H-carbazole (150 mg, 0.61 mmol) and CuCN (60 mg, 0.67 mmol) were dissolved in 3 ml of NMP and heated to 200 °C overnight. Upon completion the reaction was warmed to room temperature, diluted with 3 ml of H ₂ 0 and filtered to remove CuBr salts. The filtrate was extracted 3X with EtOAc, washed with H ₂ 0, brine, and dried over MgSOzt. The crude mixture was purified on Si0 ₂ (0 to 50% EtOAc/hexanes to afford 9-H-carbazole-3-carbonitrile.

^ NMR ^OO MHz, DMSO-i/ ₆ ) δ 1 1.87 (s, 1H), 8.71 (s, 1H), 8.24 (d, J= 7.8 Hz, 1H), 7.75 (d, J = 8.4 Hz, 1H), 7.63 (d, J= 8.4 Hz, 1H), 7.57 (d, J= 7.9 Hz, 1H), 7.49 (t, J= 7.6 Hz, 1H), 7.26 (t, J= 7.5 Hz, 1H). ESI m/z: 193.0 ([M+H] ⁺ , Ci ₃ H ₈ N ₂ requires 193.07)

Step 2: 6-bromo-9H-carbazole-3-carbonitrile (P7C3-S216)

N

9-H-carbazole-3-carbonitrile (185 mg, 0.962 mmol) and N-bromosuccinimide (171 mg, 0.92 mmol) were added to 5 ml of EtOAc and 13 ml of toluene. This mixture was stirred for 3 days at room temperature. Upon completion of the reaction, the reaction was concentrated, diluted in EtOAc, washed with NaHC0 ₃ , H ₂ 0, brine, and dried over Na ₂ SO/t. The crude mixture was purified on Si0 ₂ (0 to 50% EtOAc/hexanes to afford the desired product in 90% yield.

¹ H NMR (400 MHz, CDC1 ₃ ) δ 8.38 (s, 1H), 8.35 (s, 1H), 8.22 (s, 1H), 7.69 (dd, J= 8.5, 1.4 Hz, 1H), 7.60 (dd, J= 8.6, 1.8 Hz, 1H), 7.50 (d, J= 8.5 Hz, 1H), 7.38 (d, J= 8.6 Hz, 1H). ESI m/z: 270.9 ([M+H] ⁺ , C ₁₃ H ₇ BrN ₂ requires 270.98)

P7C3-S222: 3-amino-5-bromo-lH-indole-2-carbonitrile Stepl. Synthesis of 5-bromo-2-((cyanom le

Following Representative Procedure 1, 2-((cyanomethyl)amino)benzonitrile (Michaelidou, S. S.; Koutentis, P. A. Tetrahedron 2010, 66, 685-688) (0.020 g, 0.127 mmol) was treated with NBS (0.034 g, 0.191 mmol) in CH ₂ Cl ₂ :MeOH (1 : 1) (25 mL) to afford the title product (0.017 g, 58%).

'H NMR (CDCVMeOD [4:2], 500 MHz) δ 7.59-7.54 (m, 2H), 6.67 (d, 1H, J= 8.8 Hz). 4.16 (s, 2H). MS (ESI) m/z 235.8 [M-H] ^" ([M-H] ^" , C ₉ H ₅ BrN ₃ requires 235.0).

Step2. Synthesis of 3-amino-5-bromo-lH-indole-2-carbonitrile (P7C3-S222)

Following a literature procedure (Michaelidou, S. S.; Koutentis, P. A. Tetrahedron 2010, 66, 685- 688), 5-bromo-2-((cyanomethyl)amino)benzonitrile (0.290 g, 1.234 mmol) and K ₂ C0 ₃ (0.085 g, 0.617 mmol) were dissolved in EtOH (3.9 mL) and heated to 120 °C in a microwave reactor for 10 min. The reaction mixture was then cooled to room temperature, diluted with water and extracted with CH ₂ CI ₂ . The organic layers were dried over Na ₂ S0 ₄ , filtered and condensed. The crude mixture was purified by

chromatography (Si0 ₂ , 0-50% EtOAc/Hexanes) to afford the title compound (0.254 g, 88%).

¹ H NMR (CDCl ₃ -MeOD [4:2], 500 MHz) δ 7.46 (d, 1H, J= 1.7 Hz), 7.04 (dd, 1H, J= 1.7, 8.8

Hz), 6.83 (d, 1H, J= 8.8 Hz). MS (ESI) m/z 236.8 [M+H] ⁺ ([M+H] ⁺ , C ₉ H ₇ BrN ₃ requires 237.0).

P7C3-S224: 2-(3-bromo-6-cyano-9H-carbazol-9-yl)acetic acid

The title compound was prepared analogously to P7C3-S165.

¹ H NMR (CDC1 _{3 +} (CD ₃ ) ₂ C0, 400 MHz) δ 8.18 (d, J= 1.6 Hz, 1H), 8.04 (d, J= 1.9 Hz, 1H), 7.51 (dd, J= 8.5, 1.6 Hz, 1H), 7.40 (dd, J= 8.6, 1.9 Hz, 1H), 7.31 (d, J= 8.6 Hz, 1H), 7.17 (d, J= 8.7 Hz, 1H), 4.91 (s, 2H). MS (ESI), m/z: calculated 327.98, found 328.8 (M+l).

P7C3-S225: 6-bromo-9H-carbazole-3-carboxylic acid

P7C3-S216 (299.6 mg, 1.1 mmol) was treated with HC1 in dioxane (4.0 M, 3ml) and concentrated HC1 at 100 °C for 60 hours. The crude mixture was taken up in EtOAc, neutralized with IN NaOH and washed with brine. The organic layer was dried over Na ₂ S0 ₄ , filtered and condensed. Column chromatography in 5%

MeOH/DCM (+0.1 % formic acid) gave gave desired in 90% yield.

¹ H NMR (DMSO, 400 MHz) δ δ 1 1.69 (s, 1H), 8.75 (d, J= 1.6 Hz, 1H), 8.33 (d, J= 1.9 Hz, 1H), 7.98 (dd, J= 8.5, 1.7 Hz, 1H), 7.89 (bs, 1H), 7.62 - 7.42 (m, 2H), 7.24 (bs, 1H). MS (ESI), m/z:

calculated 288.97, found 289.8 (M+l). P7C3-S227: 6-bromo-9-(carboxymethyl)-9H-pyrido [3,4-b] indole-3-carboxylic acid

6-bromo-9-(2-ethoxy-2-oxoethyl)-9H-pyrido[3,4-b]indole-3-car boxylate

Ethyl 6-bromo-9-(2-ethoxy-2-oxoethyl)-9H-pyrido[3,4-b]indole-3-car boxylate was synthesized analogously to P7C3-S 164. The crude material was purified on S1O ₂ (0-60% EtOAc/hexanes to give the desired compound in 92% yield.

¾ NMR (500 MHz, DMSO-i/ ₆ ) δ 9.13 (s, 1H), 9.03 (s, 1H), 8.78 (s, 1H), 7.80 (dd, J= 8.8, 1.5 Hz, 1H), 7.74 (d, J= 8.9 Hz, 1H), 5.59 (s, 2H), 4.39 (q, J= 7.1 Hz, 2H), 4.21 - 4.12 (m, 2H), 1.38 (t, J = 7.1 Hz, 3H), 1.21 (t, J = 7.1 Hz, 3H). ESI m/z: 404.8 ([M+H] ⁺ , Ci ₂ H ₁₇ BrN ₂ 0 ₄ requires 405.04) - 6-bromo-9-(carboxymethyl)-9H-pyrido[3,4-b]indole-3-carboxyli c acid

6-bromo-9-(carboxymethyl)-9H-pyrido[3,4-b]indole-3-carboxyli c acid (P7C3-S227) was synthesized analogously to P7C3-S 165.

^ NMR ^OO MHz, DMSO-i/ ₆ ) 8 9.13 (s, 1H), 9.02 (s, 1H), 8.75 (s, 1H), 7.80 (d, J = 9.2 Hz, 1H), 7.75 (d, J = 8.8 Hz, 1H), 5.49 (s, 2H). ESI m/z: 348.7 ([M+H] ⁺ , Ci ₄ H ₉ BrN ₂ 0 ₄ requires 348.97) o-6-methyl-9H-carbazole

This compound was prepared according to US6018046 Al , incorporated herein by reference in its entirety. -S229: l-(9H-carbazol-9-yl)-3-(phenylamino)propan-2-ol

The title compound was prepared according to the procedure of Asso et al, ChemMedChem, 2008 1530.

MS (ESI): 317.1 [M+H] ⁺ , C ₂ iH ₂₀ N ₂ O requires 316.2.

P7C3-S230- 2-(3,6-dibromo-9H-carbazol-9-yl)-N-(phenylsulfonyl)acetamide

2-(3,6-dibromo-9H-carbazol-9-yl)-N-(phenylsulfonyl)acetamide was synthesized analogously to P7C3-S232 except benzensulfonamide was used.

^! H NMR (400 MHz, Acetone-ifc) δ 8.37 (d, J= 1.8 Hz, 2H), 8.00 (dd, J= 8.4, 1.2 Hz, 2H), 7.75 - 7.69 (m, 1H), 7.63 - 7.57 (m, 2H), 7.53 (dd, J= 8.7, 2.0 Hz, 2H), 7.38 (d, J= 8.7 Hz, 2H), 5.33 (s, 2H). ESI m/z: 518.5 ([M-H] ⁺ , C ₂ oHi ₄ Br ₂ N ₂ 0 ₃ S requires 518.91) P7C3-S231- 2-(3,6-dibromo-9H-carbazol-9-yl)-N-hydroxyacetamide

Following a published procedure (J.Med. Chem., 2011, 54, 5576-5582), ethyl 2-(3,6-dibromo-9H- carbazol-9-yl)acetate (P7C3-S 164) (50 mg, 0.12 mmol) was suspended in a 1 : 1 (v/v) mixture of methanol (500 ul) and 50% hydiOxylamine (aq.). To this suspension was added 1 N NaOH _(aq) (250 ul). Upon completion IN HCl was added, upon which the product precipitated from solution. The precipitate was further purified on Si0 ₂ (0-60% EtOAc/hexanes.) ¾ NMR (500 MHz, Acetone-i/ ₆ ) δ 8.39 (s, 2H), 7.59 (dd, J

ESI m/z: 394.5 ([M-H] ⁺ , Ci ₄ H ₁₀ Br ₂ N ₂ O2 requires 394.91)

P7C3-S232: 2-(3,6-dibromo-9H-carbazol-9-yl)-N-(methylsulfonyl)acetamide

Following a published procedure (Bioorg.Med. Chem., 2006, 1331 - 1338) a solution of 2-(3,6- dibromo-9H-carbazol-9-yl)acetic acid (P7C3-S 165) (100 mg, 0.26 mmol) in dry THF was added to a stirred solution of carbonyldiimidazole (42.3 mg, 0.261 mmol) in THF. The mixture was stirred 30 min at room temperature and 30 min at reflux. The mixture was cooled to room temperature and

methanesulfonamide (25 mg, 0.261 mmol) was added in one portion and stirred for 10 minutes. A solution of l,8-Diazabicyclo[5.4.0]undec-7-ene (40 mg, 0.261 mmol) in THF was added dropwise. The solution was stirred overnight at room temperature. The solution was poured into ice cold 1 N HCl and extracted with EtOAc. The organic layer was washed with water, brine, dried over MgS04 and concentrated. The crude material was purified on Si0 ₂ (0-50% EtOAc/hexanes.)

lU NMR (500 MHz, Acetone-i/ ₆ ) δ 8.39 (s, 2H), 7.57 (dd, J= 22.2, 8.7 Hz, 4H), 5.22 (s, 2H),

3.1 1 (s, 3H) ESI m/z: 458.5 ([M-H] ⁺ , Ci ₅ H ₁₂ Br ₂ N ₂ 0 ₃ S requires 456.89)

P7C3-S235: 2-(3,6-dibromo-9H-carbazol-9-yl)acetonitrile

r

3,6-dibromocarbazole (500 mg, 1.54 mmol) was dissolved in DMF (7.5 ml) and treated with

KOH (86 mg, 1.54 mmol) for 30 minutes. K ₂ C0 ₃ (319 mg, 2.3 mmol) and bromoacetonitrile (332 mg, 2.77 mmol) were added. The reaction was stirred overnight at room temperature. Upon addition of H ₂ 0 a precipitate formed which was filtered and purified on Si0 ₂ (0-25% EtOAc/hexanes.)

'H NMR (500 MHz, Acetone-i/ ₆ ) δ 8.47 (s, 2H), 7.74 (dd, J= 20.1, 8.7 Hz, 4H), 5.73 (s, 2H). ESI m/z: 360.6 ([M-H] ⁺ , Ci ₄ H ₈ Br ₂ N ₂ requires 360.91)

P7C3-S236: 3-bromo-9H-carbazole. This compound was purchased from SigmaAldrich. ethyl-9H-carbazole

This compound was prepared as reported in Beyer, M. et al. J. Org. Chem. 2003 (68) 2209.

P7C3-S238: 2- 3-bromo-6-carbamoyl-9H-carbazol-9-yl)acetic acid

The title compound was prepared analogously to P7C3-S165.

MS (ESI) m/z: 346.9 [M+H]+, C15H1 lBrN203 requires 346.0

P7C3-S239 : 6-bromo-9-(carboxymethyl)-9H-carbazole-3-carboxylic acid

The title compound was prepared analogously to P7C3-165

¹ H NMR (DMSO, 500 MHz) δ 13.16 (s, 1H), 8.78 (s, 1H), 8.38 (s, 1H), 8.02 (d, J= 8.6 Hz, 1H), 7.93 (s, 1H), 7.62 (d, J= 15.0 Hz, 2H), 7.29 (s, 1H), 5.29 (s, 2H).MS (ESI), m/z: calculated 346.98, found 347.9 (M+l). omo-6-methyl-9H-carbazol-9-yl)acetic acid

The title compound was prepared analogously to P7C3-165. ^l U NMR (CDCI ₃ + (CD ₃ ) ₂ CO, 400) δ 8.09 (d, J= 2.0 Hz, 1H), 7.79 (s, 1H), 7.54 (d, J= 8.6 Hz, 2H), 7.43 (dd, J= 8.7, 2.0 Hz, 1H), 7.26 (m, 1H), 4.99 (s, 2H), 2.44 (s, 3H). MS (ESI), m/z: calculated 317.01, found 318.0 (M+l). P7C3-S241: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-l,l,l-tr ifluoro-N-(3- amide

Following Representative Procedure 4, P7C3-S244 was fluorinated to give the title compound. ¾ NMR (400 MHz, CDC1 ₃ ) δ 8.15 (d, J= 1.9 Hz, 2H), 7.56 (dd, J= 8.7, 1.9 Hz, 2H), 7.32 (t, J= 8.2 Hz, 1H), 7.21 (d, J= 8.6 Hz, 2H), 6.99 - 6.90 (m, 2H), 6.86 (m, 1H), 5.08 - 4.86 (dm, 1H), 4.57 - 4.44 (m, 2H), 4.09 (m, 2H), 3.79 (s, 3H). MS (ESI), m/z: calculated 635.93, found 680.6 (M+HCOO ) ^" .

P7C3-S242: 3-indolepropionic acid.

This compound was purchased from SigmaAldrich.

P7C3-S244: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-l,l,l-t rifluoro-N-(3- methoxyphenyl)methanesulfonamide : l, l, l-trifluoro-N-(3-methoxyphenyl)methanesulfonamide

A solution of trifluoromethanesulfonic anhydride (45 ml, 26.7 mmol) in methylene chloride (250 ml) was added dropwise to an ice chilled solution of m-anisidine (25 ml, 22.3 mmol) and triethylamine (39 ml, 28.0 mmol) in methylene chloride (1.25 L). The reaction was stirred overnight at ambient temperature. Workup was performed portionwise. Each of the two portions was basified by addition of 250 ml of 2.5 N NaOH solution and 625 ml MeOH. The aqueous was extracted thrice (100 ml each) with methylene chloride. The combined aqueous phases was acidified to pH 2 with 18% HCl and again extracted with methylene chloride three times. The organic layer is dried over MgS0 ₄ , filtered and condensed to give 17.69 g of brown solid in 77% yield. ¾ NMR (CDCI ₃ , 400 MHz) 57.48-7.13 (m, 1H), 6.97-6.61 (m, 3H), 3.82 (s, 3H). MS (ESI), m/z: calculated 255.21, found 255.9 (M+l) ⁺ .

Step 2: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)- 1,1, 1 -trifluoro-N-(3- de (P7C3-S244).

N-butyllithium (2.5 M in hexanes, 48 ml) was added dropwise to an ice-cooled solution of 1, 1,1- trifluoro-N-(3-methoxyphenyl)methanesulfonamide (22.07 g, 86.5 mmol) in dry dioxane (145 ml) over a 40 minute period. The solution was then stirred at ambient temperature for 15 minutes before addition of 3,6-dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole (25.05 g, 65.7 mmol) followed by heating at 90 °C for an hour. The reaction was cooled then diluted with 1.2 L ethyl acetate and washed several times with water and finally brine. The organic layer was dried over MgSO/t, filtered and condensed to give an orange viscous mixture. The residue was dissolved in 150 ml of 60% methylene chloride/hexanes, then concentrated to yellow foam to which a further 150 ml of 60% methylene chloride/hexanes was added and stirred overnight. The mixture was filtered and washed several times with 60% methylene chloride/hexanes until the solid was white giving 20.1 g of 99%

^ NMR CDCls, 400 MHz) δ 8.13 (d, J= 1.9 Hz, 2H), 7.54 (dd, J= 8.7, 1.9 Hz, 2H), 7.33 (t, J = 8.1 Hz, 1H), 7.22 (d, J= 8.7 Hz, 2H), 6.95 (dd, J= 8.4, 2.3 Hz, 2H), 6.88 (s, 1H), 4.56 - 4.10 (m, 4H), 3.99 (m, 1H), 3.81 (s, 3H), 1.98 (d, J= 4.2 Hz, 1H). MS (ESI), m/z: calculated 633.94, found 678.6 (M+HCOO)- .

P7C3-S246: ethyl 5-tosyl-5H-pyrimido[5,4-b]indole-2-carboxylate

The title compound was synthesized following a reported procedure (Rahtz et al.

US4564610 A1). ^l U NMR (CDCI ₃ , 500 MHz) δ 9.76 (s, 1H), 8.44 (d, 1H, J= 1.1 Hz), 8.37 (d, 1H, J= 8.5 Hz), 7.80 (t, 1H, J= 7.9 Hz), 7.75 (d, 2H, J= 8.4 Hz), 7.54 (t, 1H, J= 7.5 Hz), 7.18 (d, 2H, J= 8.1 Hz), 4.60 (q, 2H, J= 7.1 Hz), 2.31 (s, 3H), 1.52 (t, 3H, J= 7.1 Hz). P7C3-S245: 2-(dimethylamino)-5H-pyrimido[5,4-b]indol-4-ol

To a suspension of 3-amino-lH-indole-2-carbonitrile (Michaelidou, S. S.; Koutentis, P. A. Tetrahedron 2010, 66, 685-688) (0.032 g, 0.200 mmol) in DCE (1.5 mL) was added Cl ₂ CN ⁺ Me ₂ Cl ^~ (0.046 g, 0.28 mmol) and the mixture was stirred under reflux overnight. Upon completion, the cooled reaction was concentrated and dissolved in AcOH (0.6 mL). Then, NH ₄ OAc (0.040 g, 0.52 mmol) was added and the mixture was stirred under reflux for 20 h. The cooled reaction was neutralized with saturated NaHCC>3 and the mixture extracted with EtOAc. The organic layers were washed with brine, dried over Na ₂ S0 ₄ , filtered and condensed. The crude mixture was purified by chromatography (Si0 ₂ , 0- 10% MeOH/CH ₂ Cl ₂ ) to afford the title compound (0.015 g, 33%).

lU NMR (CDCl ₃ -MeOD [4:2], 500 MHz) δ 7.94 (d, 1H, J= 8.0 Hz), 7.33-7.28 (m, 2H), 7.03 (t,

1H, J= 7.1 Hz), 3.08 (s, 6H). MS (ESI) m/z 229.0 [M+H] ⁺ ([M+H] ⁺ , C ₁₂ H ₁₃ N ₄ 0 requires 229.2).

P7C3-S247: ethyl 5-tosyl-4,5-dihydro-lH-pyrimido [5,4-b] indole-2-carboxylate

The title compound was synthesized following a reported procedure (Rahtz et al.

US4564610 A1).

lU NMR (CDCI ₃ , 500 MHz) δ 8.02 (d, 1H, J= 8.1 Hz), 7.75 (d, 1H, J= 1A Hz), 7.60 (d, 2H, J = 8.4 Hz), 7.34-7.21 (m, 2H), 7.18 (d, 2H, J= 8.1 Hz), 5.30 (s, 2H), 4.39 (q, 2H, J= 7.1 Hz), 2.31 (s, 3H), 1.40 (t, 3H, J= 7.1 Hz). P7C3-S248: L-tryptophan

This compound was purchased from SigmaAldrich.

P7C3-S249: L-5-hydroxy-tryptophan

This compound was purchased from SigmaAldrich

P7C3-S248: L-tryptophan methyl ester hydrochloride

This compound was purchased from SigmaAldrich P7C3-S251: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3- methoxyphenyl)methanesulfonamide

P7C3-S251 was synthesized analogously to P7C3-S244 in quantitative yield.

lH NMR (CDCI ₃ , 400 MHz) δ 8.13 (d, J= 1.6 Hz, 2H), 7.53 (dd, J= 8.8, 1.8 Hz, 2H), 7.37 - 7.30 (m, 1H), 7.26 (d, J= 7.7 Hz, 2H), 6.98 - 6.83 (m, 3H), 4.52 - 4.37 (m, 3H), 4.36 - 4.17 (m, 2H), 3.82-3.91 (m, 1H), 3.76 (s, 3H), 3.71 (s, 1H), 2.93 (s, 3H), 2.28 (d, J= 3.7 Hz, 1H). MS (ESI), m/z:

calculated 579.97, found 624.6 (M+HCOO) ^" .

P7C3-S252: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3- methoxyphenyl)benzenesulfonamide

P7C3-S252 was synthesized analogously to P7C3-S244 using representative procedure 3 and N-(3- methoxyphenyl)benzenesulfonamide and in quantitative yield.

lU NMR (CDCI ₃ , 400 MHz) δ 8.13 (d, J= 1.9 Hz, 2H), 7.67 - 7.38 (m, 8H), 7.26 (d, J= 8.7 Hz, 2H), 6.90 (dd, J= 8.4, 2.5 Hz, 1H), 6.73 - 6.55 (m, 3H), 4.50 (dd, J= 15.1, 3.4 Hz, 1H), 4.32 (dd, J =

15.1, 8.3 Hz, 1H), 4.22 (bs, 1H), 3.80 - 3.65 (m, 5H), 2.32 (d, J= 3.9 Hz, 1H). MS (ESI), m/z: calculated 641.98, found 686.6 (M+HCOO) ^" . P7C3-S253: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3-me thoxyphi

(trifluoromethyl)benzenesulfonamide

P7C3-S253 was synthesized analogously to P7C3-S244 using representative procedure 3 and N- (3-methoxyphenyl)-2-(trifluoromethyl)benzenesulfonamide and in quantitative yield.

¹ H NMR (CDCI ₃ , 400 MHz) δ) 8.1 1 (d, J= 1.9 Hz, 2H), 7.88 (d, J= 7.9 Hz, 1H), 7.72 (d, J= 8.2 Hz, 1H), 7.65 (t, J= 7.7 Hz, 1H), 7.59 - 7.42 (m, 3H), 7.36 - 7.17 (m, 2H), 7.17 (t, J= 8.1 Hz, 1H), 6.85 - 6.62 (m, 3H), 4.46 (dd, J= 15.1, 3.6 Hz, 1H), 4.32 (dd, J= 15.0, 8.4 Hz, 1H), 4.20 (bs, 1H), 3.93 (d, J = 6.1 Hz, 1H), 3.75-3.66 (m, 4H), 2.14 (d, J= 4.0 Hz, 1H). MS (ESI), m/z: calculated 709.97, found 754.5 (M+HCOO)- .

P7C3-S254: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-4-metho xy-N-(3- methoxyphenyl)benzenesulfonamide

P7C3-S254 was synthesized analogously to P7C3-S244 using representative procedure 3 and 4- methoxy-N-(3-methoxyphenyl)benzenesulfonamide and in quantitative yield.

^! H NMR (CDCI ₃ , 400 MHz) δ 8.20 - 8.01 (m, 2H), 7.52 (dd, J= 8.6, 1.8 Hz, 2H), 7.48 (d, J= 8.8 Hz, 2H), 7.23 (m, 3H), 6.91 (d, J= 8.9 Hz, 2H), 6.89 - 6.83 (m, 1H), 6.67 (t, J= 2.3 Hz, 1H), 6.63 - 6.57 (m, 1H), 4.53 - 4.39 (m, 1H), 4.37 - 4.25 (m, 1H), 4.20 (bs, 1H), 3.89 (s, 3H), 3.75 (s, 3H), 3.68 - 3.58 (m, 2H), 2.29 (d, J = 4.1 Hz, 1H). MS (ESI), m/z: calculated 671.99, found 716.5 (M+HCOO) ^" .

P7C3-S256: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-N-(3- methoxyphenyl)methanesulfonamide

P7C3-S256 was synthesized analogously to P7C3-S241 using representative procedure 4 with morpho-DAST and N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3- methoxyphenyl)methanesulfonamide and in quantitative yield.

lU NMR (CDC1 ₃ , 400 MHz) δ 8.14 (d, J= 2.1 Hz, 2H), 7.55 (dd, J= 8.6, 1.9 Hz, 2H), 7.33 (t, J =

8.0 Hz, 1H), 7.25 (d, J= 9.6 Hz, 2H), 7.01 - 6.82 (m, 3H), 4.97 (dm, J _H - _F = 49.2 Hz, 1H), 4.73 - 4.35 (m, 2H), 4.14 - 3.98 (m, 2H), 3.81 (s, 3H), 2.96 (s, 3H). MS (ESI), m/z: calculated 581.96, found 626.5

(M+HCOO)- .

P7C3-S257: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-N-(3-met hoxyphi

amide

P7C3-S257 was synthesized analogously to P7C3-S241 using representative procedure 4 with morpho- DAST and N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-N-(3-me thoxyphenyl)-2- (trifluoromethyl)benzenesulfonamide and in 95% yield.

lU NMR (CDCI ₃ , 400 MHz) δ 8.13 (d, J= 1.8 Hz, 2H), 7.90 (d, J= 7.9 Hz, 1H), 7.72 (d, J= 8.0 Hz, 1H), 7.65 (t, J= 7.8 Hz, 1H), 7.56 (dd, J= 8.7, 1.9 Hz, 2H), 7.49 (t, J= 7.8 Hz, 1H), 7.29 (d, J= 8.8 Hz, 2H), 7.16 (t, J= 8.1 Hz, 1H), 6.81 (dd, J= 8.4, 2.5 Hz, 1H), 6.78 - 6.64 (m, 2H), 4.93 (dm, J _H - _F =

48.1 Hz, 1H), 4.76 - 4.44 (m, 2H), 4.23 (t, J= 14.3 Hz, 1H), 4.06 (dd, J= 15.2, 6.1 Hz, 1H), 3.71 (s, 3H). MS (ESI), m/z: calculated 71 1.97, found 756.5 (M+HCOO) ^"

P7C3-S258: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-fluoropropyl)-4-methox y-N-(3- methoxyphenyl)benzenesulfonamide

P7C3-S258 was synthesized analogously to P7C3-S241 using representative procedure 4 with morpho-DAST and N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-4-metho xy-N-(3- methoxyphenyl)benzenesulfonamide and in quantitative yield.

lU NMR (CDC1 ₃ , 400 MHz) δ 8.14 (d, J= 1.9 Hz, 2H), 7.55 (dd, J= 8.8, 1.9 Hz, 2H), 7.51 (d, J = 8.9 Hz, 2H), 7.26 - 7.20 (m, 3H), 6.93 (d, J= 8.9 Hz, 2H), 6.88 (dd, J= 8.2, 2.5 Hz, 1H), 6.70 (t, J= 2.2 Hz, 1H), 6.64 (dt, J= 7.9, 1.4 Hz, 1H), 4.93 (dm, J _H - _F = 48.1, 6.6 Hz, 1H), 4.72 (ddd, J= 31.8, 16.0, 2.4 Hz, 1H), 4.52 (td, J= 16.9, 16.2, 8.2 Hz, 1H), 4.03 - 3.91 (m, 1H), 3.89 (s, 3H), 3.86 - 3.76 (m, 1H), 3.75 (s, 3H). MS (ESI), m/z: calculated 673.99, found 718.6 (M+HCOO) ^" .

P7C3-S262: ethyl 5H-pyrimido[5,4-b]indole-2-carboxylate

The title compound was synthesized following a reported procedure (Rahtz et al. US4564610 Al, incorporated herein by reference).

^ NMR CDCls, 400 MHz) δ 9.06 (s, 1H), 8.50 (d, lH, J= 8.0 Hz), 7.64 (ddd, 1H, J= 1.2, 7.1, 8.2 Hz), 7.56 (d, 1H, J= 8.3 Hz), 7.36 (ddd, 1H, J= 0.9, 7.1, 8.0 Hz), 4.58 (q, 2H, J= 7.1 Hz), 1.50 (t, 3H, J= 7.1 Hz).

P7C3-S264: N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)- 1, 1,1 -trifluoromethanesulfonamide

l-amino-3-(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol (100 mg, 0.2518 mmol) and triethylamine (42 μΐ., 0.3022 mmol) were dissolved in 1.7 mL DCM. The vial was cooled to 0 °C. Triflic anhydride (51 0.3022 mmol) was then added and the solution was left to react overnight. The reaction mixture was basified with 1M NaOH, and the layers were separated. The aqueous layer was washed 3x with DCM and the combined organic layers were then acidified using 18% HC1. The mixture was separated and the aqueous layer washed 3x with DCM. The combined organic layers were dried and concentrated to afford crude material as a yellow residue. This was purified by column chromatography using a gradient 60% DCM/Hex to 90% DCM/ MeOH eluent and afforded 8.8 mg (6.6% yield) of product as a white solid. ^ NMR ^OO MHz, CD ₃ OD) δ 8.23 (d, J= 2.1 Hz, 1H), 8.21 (d, J= 2.3 Hz, 1H), 7.56 (dq, J= 8.7, 1.9 Hz, 2H), 7.49 (dd, J= 8.7, 5.1 Hz, 2H), 4.40 (ddd, J= 15.3, 6.6, 3.6 Hz, 1H), 4.36 - 4.26 (m, 1H), 4.13 (s, 1H), 3.42 (dd, J= 13.7, 4.7 Hz, 1H), 3.39 - 3.32 (m, 1H). MS (ESI) m/z = 526.6 ([M-H] ^" ,

C16H13Br2F3N203S requires 527.90.

P7C3-S265: alpidem, also known as 6-Chloro-2-(4-chlorophenyl)-N,N-dipropyl-imidazo[l,2-a]pyrid ine- 3-acetamide, 6-Chloro-2-(p-chlorophenyl)-N,N-dipropylimidazo(l,2-a)pyridi ne-3-acetamide

This compound was purchased from SigmaAldrich.

P7C3-S266: TRO 19622, also known as Cholest-4-en-3-one, oxime.

This compound was purchased from SigmaAldrich.

P7C3-S267: (+)-a-tocopherol.

This compound was purchased from SigmaAldrich.

P7C3-S268: 3-amino- lH-indole-2-carbonitrile

Η ,

The title compound was made analogously to P7C3-S222. MS (ESI) m/z: 158.0 [M+H] ⁺ , C9H7N3 requires 157.1.

P7C3-S269: 8-bromo-lH-pyrimido[5,4-b]indole-2,4(3H,5H)-dione

The title compound was synthesized following a reported procedure (Reichelt et al.

US201 1/002151 1 Al, incorporated herein by reference).

'H NM ^-DMSO, 400 MHz) δ 1 1.97 (s, 1H), 1 1.57 (s, 1H), 1 1.15 (s, 1H), 8.13 (s, 1H), 7.46 (d, 1H, J= 8.9 Hz), 7.36 (d, 1H, J= 8.9 Hz). MS (ESI) m/z 281.8 [M+H] ⁺ ([M+H] ⁺ , Ci ₀ H ₇ BrN ₃ O ₂ requires 281.0).

P7C3-S270 : 8-bromo-2-(dimethylamino)-5H-pyrimido [5,4-b] indol-4-ol

P7C3-S270 was synthesized and isolated in 72% yield analogously to P7C3-S245 except P7C3- S222 was used.

^! H NMR ( -DMSO, 400 MHz) δ 1 1.60 (s, 1H), 1 1.13 (brs, 1H), 7.97 (s, 1H), 7.45 (d, 1H, J = 8.8 Hz), 7.36 (d, 1H, J= 8.8 Hz), 3.09 (s, 6H). MS (ESI) m/z 307.8 [M+H] ⁺ ([M+H] ⁺ , C ₁₂ H ₁₂ BrN ₄ 0 requires 308.1).

P7C3-S272: 8-bromo-l,3,5-trimethyl-lH-pyrimido[5,4-b]indole-2,4(3H,5H)- dione

NaH (0.087 g, of 60% suspension (in oil), 2.16 mmol) was added to a solution of P7C3-S269 (0.100 g, 0.36 mmol) in dry DMF (1.8 mL) at 0 °C and stirred for 30 min. Then, Mel (168 2.7mmol) was added dropwise to the reaction mixture. The reaction was warmed to room temperature and stirred for 3 h. Upon completion, the product was precipitated by the addition of water, collected by filtration and washed with water. The title compound was isolated as a brown solid (0.1 15 g, 99 %). H NMR (CDCl ₃ -MeOD [4:2], 500 MHz) δ 7.96 (d, 1H, J= 1.7 Hz), 7.39 (dd, 1H, J= 1.7, 9.0 Hz), 7.20 (d, 1H, J= 9.0 Hz), 3.96 (s, 3H), 3.74 (s, 3H), 3.30 (s, 3H). MS (ESI) m/z 321.8 [M-H] ^" ([M-H] ^" , CisHnBrNsOz requires 321.1).

P7C3-S275: 8-bromo-4-methoxy-N,N,5-trimethyl-5H-pyrimido[5,4-b]indol-2- amine

P7C3-S275 was synthesized and isolated in 24% yield analogously to P7C3-S272 except P7C3 S270 was used.

^ NMR CDCls, 500 MHz) δ 8.30 (d, 1H, J= 1.7 Hz), 7.53 (dd, 1H, J= 1.7, 8.8 Hz), 7.18 (d, 1H, J= 8.8 Hz), 4.10 (s, 3H), 3.93 (s, 3H), 3.25 (s, 6H). MS (ESI) m/z 336.0 [M+H] ⁺ ([M+H] ⁺ ,

Ci ₄ H ₁₆ BrN ₄ 0 requires 336.2).

P7C3-S276: 3-amino-5-methoxy-lH-indole-2-carbonitrile

Stepl. Synthesis of 2-((cyanomethyl)amino)-5-methoxybenzonitrile

Following a reported procedure (Michaelidou, S. S.; Koutentis, P. A. Tetrahedron 2010, 66, 685- 688), 2-amino-5-methoxybenzonitrile (Manetsch, R. et al. Chem. Eur. J. 2004, 10, 2487-2506) (0.109 g, 0.74 mmol) was treated with paraformaldehyde (0.024 mg, 0.81 mmol), potassium cyanide (0.053 g, 0.81 mmol), zinc chloride (0.201 g, 1.473 mmol) and sulfuric acid (1 drop) in acetic acid (2.2 mL) in a sealed tube. The mixture was then stirred at 55 °C overnight. The reaction mixture was allowed to cool to room temperature, poured onto ice and made pH neutral with Na ₂ C0 ₃ . Filtration of the precipitate gave the title compound (0.068 g, 50%).

^ NMR CDCls, 400 MHz) 8 7.1 1 (dd, 1H, J= 2.8, 9.1 Hz), 6.98 (d, lH, J= 2.8 Hz), 6.75 (d, 1H, J= 9.1 Hz), 4.15 (s, 2H), 3.74 (s, 3H).

MS (ESI) m/z 188.1 [M+H] ⁺ ([M+H] ⁺ , C ₁₀ H ₁₀ N ₃ O requires 188.2).

Step 2. Synthesis of 3-amino-5-methoxy-lH-indole-2-carbonitrile (P7C3-S276).

P7C3-S276 (Step2) was synthesized and isolated in quantitative yield analogously to P7C3-S222 (Step2) except 2-((cyanomethyl)amino)-5-methoxybenzonitrile was used.

lU NMR (CDCI ₃ , 400 MHz) 8 7.1 1 (d, 1H, J= 9.0 Hz), 6.94 (dd, 1H, J= 2.4, 9.0 Hz), 6.85 (d, 1H, J = 2.3 Hz), 3.79 (s, 3H), 2.98 (brs, 2H). MS (ESI) m/z 188.1 [M+H] ⁺ ([M+H] ⁺ , Ci ₀ H ₁₀ N ₃ O requires 188.2). -S277: l-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropyl)-3-pheny lurea

l -amino-3-(3,6-dibromo-9H-carbazol-9-yl)propan-2-ol (100 mg, 0.2518 mmol), potassium carbonate (41.8 mg, 0.3022 mmol), and phenyl isocyanate (33 μί, 0.3022 mmol) were dissolved in 5 mL THF. The reaction proceeded under inert atmosphere overnight. The reaction was quenched with water and the vial allowed to sit for one hour. A thin orange layer was carefully removed from the bottom of the vial and concentrated to give yellow residue. This was purified by column chromatography using 5% MeOH/DCM as the eluent to afford 10.1 mg (7.8% yield) of product as a translucent solid.

'H NMR (500 MHz, CD ₃ OD) δ 8.16 (s, 2H), 7.63 - 7.50 (m, 4H), 7.25 - 7.15 (m, 4H), 7.00 (d, J = 7.1 Hz, 1H), 5.16 (t, J = 6.1 Hz, 1H), 4.54 (d, J = 6.1 Hz, 2H), 2.89 (d, J= 5.8 Hz, 2H). MS (ESI) m/z = 516.0 ([M+H] ⁺ , C22H19Br2N302 requires 514.98. -S280: 3-bromo-6,9-dimethyl-9H-carbazole

3-bromo-6-methyl-9H-carbazole (100 mg, 0.3844 mmol), NaH (18 mg, 0.4497 mmol, 60%), and iodomethane (32 μΐ., 0.51 13 mmol) were dissolved in 0.3 mL DMF. The mixture was heated to 60 °C for six hours. The reaction mixture was then quenched with water to give product as a white precipitate. Product was collected via vacuum filtration and rinsed with hexanes. 85.1 mg (83.3% yield) product was collected.

¹ H NMR (400 MHz, CDC1 ₃ ) δ 8.16 (d, J= 2.0 Hz, 1H), 7.83 (dt, J= 1.7, 0.9 Hz, 1H), 7.52 (dd, J = 8.6, 2.0 Hz, 1H), 7.33 (d, J= 1.6 Hz, OH), 7.31 (d, J= 1.6 Hz, 1H), 7.30 (d, J= 0.7 Hz, 1H), 7.28 (s, OH), 7.26 (s, 1H), 7.23 (s, OH), 3.81 (s, 3H), 2.53 (s, 3H). MS (APCI) m/z = 274.0 ([M+H] ⁺ , C14H12BrN requires 273.02.

Additional compounds include:

Pro-neurogenic Efficacy / Neuroprotection Activity of Various Compounds:

Compounds were administered at a concentration of 10μΜ for each molecule. After seven days of infusion at a constant rate of 0.5 L/hour, a total of 84μΙ. of volume will have left the pump

(0.00084μΜο1β8) and entered the cerebrospinal fluid. The average volume of a brain from a 12 week old male, C57/B6 mouse in the study is 500mm . The maximal amount of drug was estimated that could potentially be present in the brain, taking the extreme and unlikely scenario of 100% absorbance of the drug into brain tissue and 0% clearance throughout the seven day infusion period. Under these conditions, at the end of one week of infusion each compound would be present at 1 ^Molar concentration. Since the actual amount of chemical compound in the brain is likely to be only a fraction of this predicted level, it is reasonable to estimate that compounds were administered at mid to low- nanomolar concentrations.

During compound infusion, animals were intraperitoneally (IP) injected daily with the thymidine analog, bromodeoxyuridine (BrdU), as a means of scoring the birth and survival of proliferating neural precursor cells in the hippocampus. Because both social interaction and voluntary exercise are known to stimulate hippocampal neurogenesis, mice were housed individually without access to running wheels throughout the screening period. Following the week-long period of compound administration, animals were perfused and sacrificed. Dissected brain tissue was fixed, embedded, sectioned, stained with antibodies to BrdU, and evaluated by light microcopy as a means of quantifying neurogenesis and survival of newborn neural precursor cells localized to the subgranular layer of the dentate gyrus on the brain hemisphere contralateral to the side of mini-pump cannulation. Every fifth section throughout the entire rostral-caudal extent of the hippocampus was analyzed, and the total number of BrdU+ cells was normalized against the measured volume of the dentate gyrus.

Intracranial infusions of either fibroblast growth factor 2 (FGF-2) or artificial cerebral spinal fluid (aCSF) vehicle via the same, week-long protocol were employed as positive and negative controls. There was no difference in the number of BrdU- labeled cells in the dentate gyrus between mice subjected to surgical pump implantation and infusion with vehicle, and mice having had no surgery.

Various compounds were tested in vivo for dose-responsive neurotrophic efficacy. The results are shown in Table 1.

Table 1. In Vivo Activity

Compounds were evaluated for pro-neurogenic efficacy / neuroprotection in a standard in vivo hippocampal neurogenesis assay at 10 μΜ concentration in four 12 week old adult male C57/B16 mice. As shown in Table 1, many compounds showed high pro-neurogenic and/or neuroprotective activity in this assay. As such, these compounds can be used to promote neurogenesis and/or reduce neuronal cell death, which are the underlying causes for a variety of neuropsychiatric and neurodegenerative diseases.

Additional methods, assays and animal models for testing pro-neurogenic and/or neuroprotective activity are decribed in detail in U.S. Pat. No. 8,362,277, U.S. Publication No. 201 1/0015217, U.S. Publication No. 2012/0022096 and U.S. Publication No. 2013/0040977, the entire disclosures of which are incorporated herein by reference in their entirety. For example, one of ordinary skill in the art would understand that the methods and animal models such as in vivo screening for pro-neurogenic compounds, structure activity relationship study, neuron survival study, neuronal apoptosis assay, mitochondrial integrity assay, aged rats model, NPAS3-deficient mice, G93A-SOD1 transgenic mice model of

Amyotrophic Lateral Sclerosis, MPTP ( 1 -methyl-4-phenyl- 1 ,2,3,6-tetrahydropyridine) toxicity model of Parkinson's disease, and R6/2 transgenic mice model of Huntington's Disease described in these patent and patent application publications can be used to further demonstrate the efficacy of the compounds described herein. Compound Forms and Salts

The compounds described herein may contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, enantiomerically enriched mixtures, single enantiomers, individual diastereomers and diastereomeric mixtures. All such isomeric forms of these compounds are expressly included in the presently disclosed embodiments. The compounds of the presently disclosed

embodiments may also contain linkages (e.g., carbon-carbon bonds, carbon-nitrogen bonds such as amide bonds) wherein bond rotation is restricted about that particular linkage, e.g. restriction resulting from the presence of a ring or double bond. Accordingly, all cis/trans and E/Z isomers and rotational isomers are expressly included in the presently disclosed embodiments. The compounds of the presently disclosed embodiments may also be represented in multiple tautomeric forms, in such instances, the presently disclosed embodiments expressly include all tautomeric forms of the compounds described herein, even though only a single tautomeric form may be represented. All such isomeric forms of such compounds are expressly included in the presently disclosed embodiments.

Optical isomers can be obtained in pure form by standard procedures known to those skilled in the art, and include, but are not limited to, diastereomeric salt formation, kinetic resolution, and asymmetric synthesis. See, for example, Jacques, et al., Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen, S.H., et al., Tetrahedron 33:2725 (1977); Eliel, E.L.

Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); Wilen, S.H. Tables of Resolving Agents and Optical Resolutions p. 268 (E.L. Eliel, Ed., Univ. of Notre Dame Press, Notre Dame, IN 1972), each of which is incorporated herein by reference in their entireties. It is also understood that the presently disclosed embodiments encompass all possible regioisomers, and mixtures thereof, which can be obtained in pure form by standard separation procedures known to those skilled in the art, and include, but are not limited to, column chromatography, thin-layer chromatography, and high-performance liquid chromatography.

The compounds of the presently disclosed embodiments include the compounds themselves, as well as their salts and their prodrugs, if applicable. A salt, for example, can be formed between an anion and a positively charged substituent (e.g., amino) on a compound described herein. Suitable anions include chloride, bromide, iodide, sulfate, nitrate, phosphate, citrate, methanesulfonate, trifluoroacetate, and acetate. Likewise, a salt can also be formed between a cation and a negatively charged substituent (e.g., carboxylate) on a compound described herein. Suitable cations include sodium ion, potassium ion, magnesium ion, calcium ion, and an ammonium cation such as tetramethylammonium ion. Examples of prodrugs include Q_6 alkyl esters of carboxylic acid groups, which, upon administration to a subject, are capable of providing active compounds.

Pharmaceutically acceptable salts of the compounds of the presently disclosed embodiments include those derived from pharmaceutically acceptable inorganic and organic acids and bases. As used herein, the term "pharmaceutically acceptable salt" refers to a salt formed by the addition of a pharmaceutically acceptable acid or base to a compound disclosed herein. As used herein, the phrase "pharmaceutically acceptable" refers to a substance that is acceptable for use in pharmaceutical applications from a toxicological perspective and does not adversely interact with the active ingredient.

Examples of suitable acid salts include acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptanoate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, palmoate, pectinate, persulfate, 3- phenylpropionate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate, tartrate, thiocyanate, tosylate and undecanoate. Other acids, such as oxalic, while not in themselves

pharmaceutically acceptable, may be employed in the preparation of salts useful as intermediates in obtaining the compounds of the presently disclosed embodiments and their pharmaceutically acceptable acid addition salts. Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N- (alky 1) ₄ ⁺ salts. The presently disclosed embodiments also envision the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispersible products may be obtained by such quaternization. Salt forms of the compounds of any of the formulae herein can be amino acid salts of carboxyl groups (e.g. L-arginine, - lysine, -histidine salts).

Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418; Journal of Pharmaceutical Science, 66, 2 (1977); and "Pharmaceutical Salts: Properties, Selection, and Use A Handbook; Wermuth, C. G. and Stahl, P. H. (eds.) Verlag Helvetica Chimica Acta, Zurich, 2002 [ISBN 3-906390-26-8] each of which is incorporated herein by reference in their entireties.

The neutral forms of the compounds may be regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner. The parent form of the compound differs from the various salt forms in certain physical properties, such as solubility in polar solvents, but otherwise the salts are equivalent to the parent form of the compound for the purposes of the presently disclosed embodiments.

In addition to salt forms, the presently disclosed embodiments provide compounds which are in a prodrug form. Prodrugs of the compounds described herein are those compounds that undergo chemical changes under physiological conditions to provide the compounds of the presently disclosed

embodiments. Additionally, prodrugs can be converted to the compounds of the presently disclosed embodiments by chemical or biochemical methods in an ex vivo environment. For example, prodrugs can be slowly converted to the compounds of the presently disclosed embodiments when placed in a transdermal patch reservoir with a suitable enzyme or chemical reagent. Prodrugs are often useful because, in some situations, they may be easier to administer than the parent drug. They may, for instance, be more bioavailable by oral administration than the parent drug. The prodrug may also have improved solubility in pharmacological compositions over the parent drug. A wide variety of prodrug derivatives are known in the art, such as those that rely on hydrolytic cleavage or oxidative activation of the prodrug. An example, without limitation, of a prodrug would be a compound of the presently disclosed embodiments which is administered as an ester (the "prodrug"), but then is metabolically hydrolyzed to the carboxylic acid, the active entity. Additional examples include peptidyl derivatives of a compound of the presently disclosed embodiments.

The presently disclosed embodiments also include various hydrate and solvate forms of the compounds.

The compounds of the presently disclosed embodiments may also contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute such compounds. For example, the compounds may be radiolabeled with radioactive isotopes, for example tritium ( ³ H), iodine- 125 ( ¹²⁵ I) or carbon- 14 ( ¹⁴ C). All isotopic variations of the compounds of the presently disclosed embodiments, whether radioactive or not, are intended to be encompassed within the scope of the presently disclosed embodiments.

SYNTHESIS

The compounds of the presently disclosed embodiments can be conveniently prepared in accordance with the procedures outlined herein, from commercially available starting materials, compounds known in the literature, or readily prepared intermediates, by employing standard synthetic methods and procedures known to those skilled in the art. Standard synthetic methods and procedures for the preparation of organic molecules and functional group transformations and manipulations can be readily obtained from the relevant scientific literature or from standard textbooks in the field. It will be appreciated that where typical or preferred process conditions (i.e., reaction temperatures, times, mole ratios of reactants, solvents, pressures, etc.) are given, other process conditions can also be used unless otherwise stated. Optimum reaction conditions may vary with the particular reactants or solvent used, but such conditions can be determined by one skilled in the art by routine optimization procedures. Those skilled in the art of organic synthesis will recognize that the nature and order of the synthetic steps presented may be varied for the purpose of optimizing the formation of the compounds described herein.

Synthetic chemistry transformations (including protecting group methodologies) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R.C. Larock, Comprehensive Organic Transformations, 2d.ed., Wiley-VCH Publishers (1999); P.G.M. Wuts and T.W. Greene, Protective Groups in Organic Synthesis, 4th Ed., John Wiley and Sons (2007); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995), and subsequent editions thereof.

The processes described herein can be monitored according to any suitable method known in the art. For example, product formation can be monitored by spectroscopic means, such as nuclear magnetic resonance spectroscopy (e.g., ^l H or ¹³ C), infrared spectroscopy (FT-IR), spectrophotometry (e.g., UV- visible), or mass spectrometry (MS), or by chromatography such as high performance liquid

chromatography (HPLC) or thin layer chromatography (TLC).

Preparation of compounds can involve the protection and deprotection of various chemical groups. The need for protection and deprotection, and the selection of appropriate protecting groups can be readily determined by one skilled in the art. The chemistry of protecting groups can be found, for example, in Greene, et al., Protective Groups in Organic Synthesis, 2d. Ed., Wiley & Sons, 1991, which is incorporated herein by reference in its entirety.

The reactions of the processes described herein can be carried out in suitable solvents which can be readily selected by one of skill in the art of organic synthesis. Suitable solvents can be substantially nonreactive with the starting materials (reactants), the intermediates, or products at the temperatures at which the reactions are carried out, i.e., temperatures which can range from the solvent's freezing temperature to the solvent's boiling temperature. A given reaction can be carried out in one solvent or a mixture of more than one solvents. Depending on the particular reaction step, suitable solvents for a particular reaction step can be selected.

Resolution of racemic mixtures of compounds can be carried out by any of numerous methods known in the art. An examplary method includes preparation of the Mosher's ester or amide derivative of the corresponding alcohol or amine, respectively. The absolute configuration of the ester or amide is then determined by proton and/or ¹⁹ F NMR spectroscopy. An examplary method includes fractional recrystallization using a "chiral resolving acid" which is an optically active, salt- forming organic acid. Suitable resolving agents for fractional recrystallization methods are, for example, optically active acids, such as the D and L forms of tartaric acid, diacetyltartaric acid, dibenzoyltartaric acid, mandelic acid, malic acid, lactic acid or the various optically active camphorsulfonic acids. Resolution of racemic mixtures can also be carried out by elution on a column packed with an optically active resolving agent (e.g., dinitrobenzoylphenylglycine). Suitable elution solvent compositions can be determined by one skilled in the art.

In certain embodiments, compounds or intermediates thereof maybe synthesized by the following representative scheme.

"(hei&rojafyl

. (heterojarvi {heterojaryl OB

In the above scheme, "(hetero)aryl" means an aryl or heteroaryl group. R, R ² , R ³ , R ⁴ and R ⁵ represent generic groups or substutients suitable for the corresponding chemical compound or reaction, as one of ordinary skill in organic chemistry would understand. For example, R togenther with the nitrogen it is connected to can form a C4 or C6 ring, which can be connected to one or more aryl and/or heteroaryl (e.g., optionally substituted phenyl, pyridine or pyrimidine). Groups R ² , R ³ and R ⁵ may be any group that can form a bond with nitrogen as generally known in the art, such as alkyl, alkenyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and/or sulfonyl, each optionally substituted with one or more halo, hydroxyl, alkoxyl, carboxyl, alkoxycarbonyl, amine, cyano, azide, sulfonyl, alkyl, alkenyl, cycloalkyl, aryl and/or heteroaryl. R ⁴ -M may be a salt in which R ⁴ is a nucleophilic group, such as a negatively charged alkyl group, and M is a positively chaged ion such as a metal ion.

Additional synthesis procedures are decribed in detail in U.S. Pat. No. 8,362,277, U.S.

Publication No. 201 1/0015217, U.S. Publication No. 2012/0022096 and U.S. Publication No.

2013/0040977, the entire disclosures of which are incorporated herein by reference in their entirety. PHARMACEUTICAL COMPOSITIONS

The term "pharmaceutically acceptable carrier" refers to a carrier or adjuvant that may be administered to a subject (e.g., a patient), together with a compound of the presently disclosed embodiments, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.

Pharmaceutically acceptable carriers, adjuvants and vehicles that may be used in the

compositions of the presently disclosed embodiments include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-a- tocopherol polyethyleneglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts, or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat. Cyclodextrins such as α-, β-, and γ-cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3-hydroxypropyl-P- cyclodextrins, or other solubilized derivatives may also be advantageously used to enhance delivery of compounds of the formulae described herein.

The compositions for administration can take the form of bulk liquid solutions or suspensions, or bulk powders. More commonly, however, the compositions are presented in unit dosage forms to facilitate accurate dosing. The term "unit dosage forms" refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient. Typical unit dosage forms include prefilled, premeasured ampules or syringes of the liquid compositions or pills, tablets, capsules, losenges or the like in the case of solid compositions. In such compositions, the compound is usually a minor component (from about 0.1 to about 50% by weight or preferably from about 1 to about 40% by weight) with the remainder being various vehicles or carriers and processing aids helpful for forming the desired dosing form.

The amount administered depends on the compound formulation, route of administration, etc. and is generally empirically determined in routine trials, and variations will necessarily occur depending on the target, the host, and the route of administration, etc. Generally, the quantity of active compound in a unit dose of preparation may be varied or adjusted from about 1, 3, 10 or 30 to about 30, 100, 300 or 1000 mg, according to the particular application. In a particular embodiment, unit dosage forms are packaged in a multipack adapted for sequential use, such as blisterpack, comprising sheets of at least 6, 9 or 12 unit dosage forms. The actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage for a particular situation is within the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small amounts until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day if desired.

The following are examples (Formulations 1-4) of capsule formulations.

Capsule Formulations

( apsii k- f oi mulaiio l l-ormu luiion 1 : I ^' orimilulion 2: I ^' orimilulion 1 oi mulai ion 4:

my apsule my capsu le my capsu le my capsu le

Compound (solid 100 400 400 200 solution)

Silicon Dioxide 0.625 2.5 3.75 1.875

Magnesium Stearate : 0.125 0.5 0.125 0.625

NF2

Croscarmellose Sod ium 1 1.000 44.0 40.0 20.0

NF

Pluronic F68 NF 6.250 25.0 50.0 25.0

Silicon Dioxide NF 0.625 2.5 3.75 1.875

Magnesium Stearate ; NF 0.125 0.5 1.25 0.625

Total 1 18.750 475.00 475.00 475.00

Capsule Size No.4 No.O No.O No.2

Preparation of Solid Solution

Crystalline compound (e.g., 80 g/batch) and the povidone (NF K29/32 at 160 g/batch) are dissolved in methylene chloride (5000 mL). The solution is dried using a suitable solvent spray dryer and the residue reduced to fine particles by grinding. The powder is then passed through a 30 mesh screen and confirmed to be amorphous by x-ray analysis.

The solid solution, silicon dioxide and magnesium stearate are mixed in a suitable mixer for 10 minutes. The mixture is compacted using a suitable roller compactor and milled using a suitable mill fitted with 30 mesh screen. Croscarmellose sodium, Pluronic F68 and silicon dioxide are added to the milled mixture and mixed further for 10 minutes. A premix is made with magnesium stearate and equal portions of the mixture. The premix is added to the remainder of the mixture, mixed for 5 minutes and the mixture encapsulated in hard shell gelatin capsule shells.

USE

In one aspect, methods for treating (e.g., controlling, relieving, ameliorating, alleviating, or slowing the progression of) or methods for preventing (e.g., delaying the onset of or reducing the risk of developing) one or more diseases, disorders, or conditions caused by, or associated with, aberrant (e.g., insufficient) neurogenesis or accelerated neuron cell death in a subject in need thereof are featured. The methods include administering to the subject an effective amount of a compound of formula (I) (and/or a compound of any of the other formulae described herein) or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein to the subject.

In another aspect, the use of a compound any of the other described herein or a salt (e.g., a pharmaceutically acceptable salt) thereof as defined anywhere herein in the preparation of, or for use as, a medicament for the treatment (e.g., controlling, relieving, ameliorating, alleviating, or slowing the progression of) or prevention (e.g., delaying the onset of or reducing the risk of developing) of one or more diseases, disorders, or conditions caused by, or associated with, aberrant (e.g., insufficient) neurogenesis or exacerbated neuronal cell death is featured.

In some embodiments, the one or more diseases, disorders, or conditions can include

neuropathies, nerve trauma, and neurodegenerative diseases. In some embodiments, the one or more diseases, disorders, or conditions can be diseases, disorders, or conditions caused by, or associated with aberrant (e.g., insufficient) neurogenesis (e.g., aberrant hippocampal neurogenesis as is believed to occur in neuropsychiatric diseases) or accelerated death of existing neurons. Examples of the one or more neuropsychiatric and neurodegenerative diseases include, but are not limited to, schizophrenia,major depression, bipolar disorder, normal aging, epilepsy, traumatic brain injury, post-traumatic stress disorder, Parkinson's disease, Alzheimer's disease, Down syndrome, spinocerebellar ataxia, amyotrophic lateral sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, and abuse of neuro-active drugs (such as alcohol, opiates, methamphetamine, phencyclidine, and cocaine), retinal degeneration, spinal cord injury, peripheral nerve injury, physiological weight loss associated with various conditions, and cognitive decline associated with normal aging, radiation therapy, and chemotherapy. The resultant promotion of neurogenesis or survival of existing neurons ( i.e. a resultant promotion of survival, growth, development, function and/or generation of neurons) may be detected directly, indirectly or inferentially from an improvement in, or an amelioration of one or more symptoms of the disease or disorder caused by or associated with aberrant neurogenesis or survival of existing neurons. Suitable assays which directly or indirectly detect neural survival, growth, development, function and/or generation are known in the art, including axon regeneration in rat models (e.g. Park et al., Science. 2008 Nov 7; 322:963-6), nerve regeneration in a rabbit facial nerve injury models (e.g. Zhang et al., J Transl Med. 2008 Nov 5;6(1):67); sciatic nerve regeneration in rat models (e.g. Sun et al., Cell Mol Neurobiol. 2008 Nov 6); protection against motor neuron degeneration in mice (e.g. Poesen et al., J. Neurosci. 2008 Oct

15;28(42) : 10451 -9); rat model of Alzheimer's disease, (e.g. Xuan et al., Neurosci Lett. 2008 Aug 8;440(3):331-5); animal models of depression (e.g. Schmidt et al., Behav Pharmacol. 2007 Sep; 18(5- 6):391-418; Krishnan et al., Nature 2008, 455, 894-902); and/or those exemplified herein.

ADMINISTRATION

The compounds and compositions described herein can, for example, be administered orally, parenterally (e.g., subcutaneously, intracutaneously, intravenously, intramuscularly, intraarticularly, intraarterially, intrasynovially, intrasternally, intrathecally, intralesionally and by intracranial injection or infusion techniques), by inhalation spray, topically, rectally, nasally, buccally, vaginally, via an implanted reservoir, by injection, subdermally, intraperitoneally, transmucosally, or in an ophthalmic preparation, with a dosage ranging from about 0.01 mg/kg to about 1000 mg/kg, (e.g., from about 0.01 to about 100 mg/kg, from about 0.1 to about 100 mg/kg, from about 1 to about 100 mg/kg, from about 1 to about 10 mg/kg) every 4 to 120 hours, or according to the requirements of the particular drug. The

interrelationship of dosages for animals and humans (based on milligrams per meter squared of body surface) is described by Freireich et al., Cancer Chemother. Rep. 50, 219 (1966). Body surface area may be approximately determined from height and weight of the patient. See, e.g., Scientific Tables, Geigy Pharmaceuticals, Ardsley, New York, 537 (1970). In certain embodiments, the compositions are administered by oral administration or administration by injection. The methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect. Typically, the pharmaceutical compositions of the presently disclosed embodiments will be administered from about 1 to about 6 times per day or alternatively, as a continuous infusion. Such administration can be used as a chronic or acute therapy.

Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of

administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.

Upon improvement of a patient's condition, a maintenance dose of a compound, composition or combination of the presently disclosed embodiments may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level. Patients may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.

In some embodiments, the compounds described herein can be coadministered with one or more other therapeutic agents. In certain embodiments, the additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of the presently disclosed embodiments (e.g., sequentially, e.g., on different overlapping schedules with the administration of one or more compounds of formula (I) (including any subgenera or specific compounds thereof)). In other embodiments, these agents may be part of a single dosage form, mixed together with the compounds of the presently disclosed embodiments in a single composition. In still another embodiment, these agents can be given as a separate dose that is administered at about the same time that one or more compounds of formula (I)

(including any subgenera or specific compounds thereof) are administered (e.g., simultaneously with the administration of one or more compounds of formula (I) (including any subgenera or specific compounds thereof)). When the compositions of the presently disclosed embodiments include a combination of a compound of the formulae described herein and one or more additional therapeutic or prophylactic agents, both the compound and the additional agent can be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen.

The compositions of the presently disclosed embodiments may contain any conventional nontoxic pharmaceutically-acceptable carriers, adjuvants or vehicles. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form.

The compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents (for example, Tween 80) and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono- or diglycerides. Fatty acids, such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions. These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions. Other commonly used surfactants such as Tweens or Spans and/or other similar emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation.

The compositions of the presently disclosed embodiments may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions. In the case of tablets for oral use, carriers which are commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried corn starch. When aqueous suspensions and/or emulsions are administered orally, the active ingredient may be suspended or dissolved in an oily phase is combined with emulsifying and/or suspending agents. If desired, certain sweetening and/or flavoring and/or coloring agents may be added.

The compositions of the presently disclosed embodiments may also be administered in the form of suppositories for rectal administration. These compositions can be prepared by mixing a compound of the presently disclosed embodiments with a suitable non-irritating excipient which is solid at room temperature but liquid at the rectal temperature and therefore will melt in the rectum to release the active components. Such materials include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.

Topical administration of the compositions of the presently disclosed embodiments is useful when the desired treatment involves areas or organs readily accessible by topical application. For application topically to the skin, the composition should be formulated with a suitable ointment containing the active components suspended or dissolved in a carrier. Carriers for topical administration of the compounds of the presently disclosed embodiments include, but are not limited to, mineral oil, liquid petroleum, white petroleum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water. Alternatively, the composition can be formulated with a suitable lotion or cream containing the active compound suspended or dissolved in a carrier with suitable emulsifying agents. Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water. The compositions of the presently disclosed embodiments may also be topically applied to the lower intestinal tract by rectal suppository formulation or in a suitable enema formulation.

In some embodiments, topical administration of the compounds and compositions described herein may be presented in the form of an aerosol, a semi-solid pharmaceutical composition, a powder, or a solution. By the term "a semi-solid composition" is meant an ointment, cream, salve, jelly, or other pharmaceutical composition of substantially similar consistency suitable for application to the skin. Examples of semi-solid compositions are given in Chapter 17 of The Theory and Practice of Industrial Pharmacy, Lachman, Lieberman and Kanig, published by Lea and Febiger (1970) and in Remington's Pharmaceutical Sciences, 21 st Edition (2005) published by Mack Publishing Company, which is incorporated herein by reference in its entirety.

Topically-transdermal patches are also included in the presently disclosed embodiments. Also within the presently disclosed embodiments is a patch to deliver active chemotherapeutic combinations herein. A patch includes a material layer (e.g., polymeric, cloth, gauze, bandage) and the compound of the formulae herein as delineated herein. One side of the material layer can have a protective layer adhered to it to resist passage of the compounds or compositions. The patch can additionally include an adhesive to hold the patch in place on a subject. An adhesive is a composition, including those of either natural or synthetic origin, that when contacted with the skin of a subject, temporarily adheres to the skin. It can be water resistant. The adhesive can be placed on the patch to hold it in contact with the skin of the subject for an extended period of time. The adhesive can be made of a tackiness, or adhesive strength, such that it holds the device in place subject to incidental contact, however, upon an affirmative act (e.g., ripping, peeling, or other intentional removal) the adhesive gives way to the external pressure placed on the device or the adhesive itself, and allows for breaking of the adhesion contact. The adhesive can be pressure sensitive, that is, it can allow for positioning of the adhesive (and the device to be adhered to the skin) against the skin by the application of pressure (e.g., pushing, rubbing,) on the adhesive or device.

The compositions of the presently disclosed embodiments may be administered by nasal aerosol or inhalation. Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.

A composition having the compound of the formulae herein and an additional agent (e.g., a therapeutic agent) can be administered using any of the routes of administration described herein. In some embodiments, a composition having the compound of the formulae herein and an additional agent (e.g., a therapeutic agent) can be administered using an implantable device. Implantable devices and related technology are known in the art and are useful as delivery systems where a continuous, or timed- release delivery of compounds or compositions delineated herein is desired. Additionally, the implantable device delivery system is useful for targeting specific points of compound or composition delivery (e.g., localized sites, organs). Negrin et al., Biomaterials, 22(6):563 (2001). Timed-release technology involving alternate delivery methods can also be used in the presently disclosed embodiments. For example, timed-release formulations based on polymer technologies, sustained-release techniques and encapsulation techniques (e.g., polymeric, liposomal) can also be used for delivery of the compounds and compositions delineated herein.

In an aspect, compounds of the presently disclosed embodiments may include those represented by formula (I):

wherein:

R ² and R ³ , together with CI and C2, form the optionally substituted phenyl, pyridine or pyrimidine ring of formulas (II)-(IV) described below, or are defined as R ^2d and R ^3d of formula (V), respectively;

R ⁴ is defined as any one of R ^4a -R ^4d in formulas (II)-(IV); and

n is 0 or 2.

For example, a compound or pharmaceutically acceptable salt thereof, for promoting

neurogenesis and/or reducing neuronal cell death, can be represented by formula (II):

wherein R ^la is selected from the group consisting of: -CH ₂ -C(0)-Z ^la and -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ - Z ^2a ; and

R ^3a and R ^4a are each independently selected from the group consisting of: hydrogen, halo, hydroxyl, Q_3 alkoxyl, cyano, carboxyl, and formamide;

wherein Z ^la is selected from the group consisting of: hydroxyl; Q_6 alkoxyl; amine optionally substituted with 1 or more Q_i ₂ alkyl, C ₂ _i ₂ alkenyl, C3_i ₂ cycloalkyl, Ci_i ₂ sulfonyl optionally substituted with 1-6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo, C4_i ₂ heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂ _i ₂ carbonyl optionally substituted with 1-6 halo, and/or C ₂ _i ₂ carboxyalkyl optionally substituted with 1-6 halo; C _{2 2} heterocyclyi; C ₆ _i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; wherein one of R and R is hydroxyl, halo, or amine optionally substituted with 1 or more Q_6 alkyl, C ₂ -6 alkenyl, C3.6 cycloalkyl, C ₂ -6 heterocyclyl, e-u aryl, and/or C ₄₄₂ heteroaryl; and the other of R ^A1 and R ^A2 is hydrogen;

wherein Z ^2a is selected from the group consisting of: halo, 0(R ^a ), S(R ^b ) and N(R ^c )(R ^d ); wherein R ^a and R ^b are each independently selected from the group consisting of: C1 2 alkyl; C ₂ - ₁₂ alkenyl; C3 2 cycloalkyl; C ₂ -6 heterocyclyl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl;

wherein R ^c and R ^d are each independently selected from the group consisting of:

hydrogen; C1 2 alkyl; C ₂ _i ₂ alkenyl; C ₃ _i ₂ cycloalkyl; C ₂ _6 heterocyclyl; C ₆ _i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; and Cz _t _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; or wherein R ^c and R ^d together with the nitrogen they are attached to form a C _4- i ₄ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or Ci_6 alkoxyl.

In some embodiments, one or more of the following definitions apply:

(6) R ^3a and R ^4a are both hydro gen or both bromo;

(7) Z ^la is hydroxyl or amine optionally substituted with 1 or more C142 alkyl, C ₂ - ₁₂ alkenyl,

and/or C _{3 2} cycloalkyl;

(8) one of R ^A1 and R ^A2 is hydroxyl or halo; and the other of R ^A1 and R ^A2 is hydrogen;

(9) Z ^2a is 0(R ^a ) or S(R ^b ); and/or

(10) Z ^2a is N(R ^c )(R ^d ). For example, R ^la may be -CH ₂ -C(0)-Z ^la or -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2a .

When R ^la is -CH ₂ -C(0)-Z ^la , Z ^la may be hydroxyl or d_ ₆ alkoxyl. Z ^la may also be amine optionally substituted with 1 or more Q42 alkyl, C ₂ _i ₂ alkenyl, C ₃ _i ₂ cycloalkyl, Ci_i ₂ sulfonyl optionally substituted with 1-6 halo, C _{6 2} aryl sulfonyl optionally substituted with 1-6 halo, C442 heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂₄₂ carbonyl optionally substituted with 1-6 halo, and/or C242 carboxyalkyl optionally substituted with 1-6 halo. For example, Z ^la can be amine optionally substituted with 1 or more Q ₄₂ alkyl, C ₂₄₂ alkenyl, and/or C ₃₄₂ cycloalkyl. Z ^la may also be C ₂₄₂ heterocyclyl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; or C ₄₄₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl.

When R ^la is -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2a , both of R ^A1 and R ^A2 can be hydrogen. Alternatively, one of R ^A1 and R^ is hydroxyl, halo (e.g., fluoro), or amine optionally substituted with 1 or more Ci_6 alkyl (e.g., methyl), C ₂ -6 alkenyl, C3.6 cycloalkyl, C ₂ -6 heterocyclyl, C6-i ₂ aryl, and/or C4_i ₂ heteroaryl; and the other of R ^A1 and R ^A2 is hydrogen. Z ^2a can be halo, 0(R ^a ), S(R ^b ) or N(R ^c )(R ^d ). R ^a and R ^b are each common substitutients such as: C n alkyl; C ₂ - ₁₂ alkenyl; C3 2 cycloalkyl; C ₂ -6 heterocyclyl; Ce-^ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl; and C4 2 heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_6 alkoxyl. R ^c and R ^d can both be hydrogen or each common substitutients such as: C n alkyl; C2-12 alkenyl; C3 2 cycloalkyl; C2-6 heterocyclyl; Ce-n aryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl; and C ₄ _i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl.

Alternatively, R ^c and R ^d together with the nitrogen they are attached to can form a ring structure, such as a C ₄ _i4 heteroaryl optionally substituted with 1 or more halo, hydroxyl, Ci_ ₆ alkyl and/or Ci_ ₆ alkoxyl.

R ^3a may be hydrogen, halo (e.g., bromo), hydroxyl, Q_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^3a is hydrogen. In some embodiments, R ^3a is bromo.

R ^4a may be hydrogen, halo (e.g., bromo), hydroxyl, Q_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^4a is hydrogen. In some embodiments, R ^4a is bromo.

In certain embodiments, the presently disclosed embodiments include a compound or pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the compound having formula (III):

wherein R is selected from the group consisting of: hydrogen; Ci_6 alkyl optionally substituted with 1 or more halo, hydroxyl, cyano and/or azide; -CH(R ⁵ )-C(0)-Z ^lb ; and -CH ₂ -C(R ^A1 )(R ^A2 )- CH ₂ -Z ^2b ;

wherein R ⁵ is hydrogen or Ci_3 alkyl;

wherein one of R ^A1 and R ^A2 is hydroxyl or halo and the other is hydrogen;

wherein Z ^lb is selected from the group consisting of: hydroxyl; Q_6 alkoxyl; and amine optionally substituted with a hydroxyl, C1 2 sulfonyl optionally substituted with 1-6 halo, C ₆ _i2 aryl sulfonyl optionally substituted with 1-6 halo, C ₄ _i ₂ heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂ -i ₂ carbonyl optionally substituted with 1-6 halo, and/or C ₂ - ₁₂ carboxyalkyl optionally substituted with 1-6 halo;

wherein Z ^2b is selected from the group consisting of: Q_3 alkyl, azide, and N(R ⁶ )(R ⁷ ); wherein R ⁶ and R ⁷ are each independently selected from the group consisting of:

hydrogen; carboxamide optionally substituted with 1 or more Ci_6 alkyl, Ce-n aryl and/or Cz _t _i ₂ heteroaryl; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_ ₆ alkoxyl; Ci_i ₂ sulfonyl optionally substituted with 1-6 halo; C ₆ _i ₂ aryl sulfonyl optionally substituted with 1-6 halo; and C ₄ _i ₂ heteroaryl sulfonyl optionally substituted with 1-6 halo; wherein no more than one of R ⁶ and R ⁷ is hydrogen; and wherein R ^3b and R ^4b are each independently selected from the group consisting of: hydrogen, halo, hydroxyl, Ci_3 alkoxyl, cyano, carboxyl, and formamide.

In some embodiments, one or more of the following definitions apply:

(5) when R ^lb is optionally substituted Ci_6 alkyl, R ^lb is selected from unsubstituted Ci_6 alkyl or C3_6 alkyl substituted with 1 hydroxyl or Ci_6 alkyl substituted with 1 cyano;

(6) when R ^lb unsubstituted Ci_6 alkyl, R ^lb is unsubstituted C ₂ -6 alkyl;

(7) when R ⁵ is hydrogen, Z ^lb is amine optionally substituted with a hydroxyl, sulfonyl optionally substituted with 1-6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo, C4 2 heteroaryl sulfonyl optionally substituted with 1-6 halo, C ₂ -i ₂ carbonyl optionally substituted with 1-6 halo, and/or C ₂ - ₁₂ carboxyalkyl optionally substituted with 1-6 halo; and/or

(8) Z ^2b is azide or N(R ⁶ )(R ⁷ ).

For example, R may be hydrogen. R may also be Ci_6 alkyl optionally substituted with 1 or more halo, hydroxyl, cyano and/or azide, such as unsubstituted Ci_6 alkyl (e.g., methyl, ethyl, n-propyl, isopropyl, or tert-butyl) or C ₃ _ ₆ alkyl substituted with 1 hydroxyl (e.g., at the beta-carbon) or Ci_ ₆ alkyl substituted with 1 cyano. R ^lb may also be -CH(R ⁵ )-C(0)-Z ^lb or -CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -Z ^2b .

R ⁵ can be hydrogen or Ci_ ₃ alkyl (e.g., methyl). Z ^lb can be hydroxyl or Ci_ ₆ alkoxyl. Z ^lb can also be amine optionally substituted with 1 hydroxyl, or amine optionally substituted with C1 2 sulfonyl, C ₆ _i ₂ aryl sulfonyl, C _4- i2 heteroaryl sulfonyl, C ₂ -i ₂ carbonyl, or C ₂ - ₁₂ carboxyalkyl (e.g., -CH ₂ C(0)OH). The Ci_ ₁₂ sulfonyl, e-u aryl sulfonyl, heteroaryl sulfonyl, C ₂ - ₁₂ carbonyl, and C ₂ - ₁₂ carboxyalkyl groups can contain one or more common substitutients such as alkyl, halo, hydroxyl, alkoxyl, aryl and/or heteroaryl.

One of R ^A1 and R ^A2 can be hydroxyl or halo (e.g., fluoro) and the other of R ^A1 and R^ can be hydrogen. Alternatively, both R ^A1 and R ^A2 can be hydrogen. Z ^2b can be Q_3 alkyl. Z ^2b can also be azide or N(R ⁶ )(R ⁷ ). R ⁶ and R ⁷ can both be hydrogen. Alternatively, only one of R ⁶ and R ⁷ is hydrogen, or none of R ⁶ and R ⁷ is hydrogen. R ⁶ and R ⁷ can also be carboxamide optionally substituted with 1 or more Q_6 alkyl, C6-i ₂ aryl and/or C4 2 heteroaryl; C6-i ₂ aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or Ci_ ₆ alkoxyl; C n sulfonyl optionally substituted with 1-6 halo; C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo; or C4 2 heteroaryl sulfonyl optionally substituted with 1-6 halo.

R ^3b may be hydrogen, halo (e.g., bromo), hydroxyl, Ci_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^3b is hydrogen. In some embodiments, R ^3b is bromo.

_R 4b

may be hydrogen, halo (e.g., bromo), hydroxyl, Ci_3 alkoxyl (e.g., methoxyl), cyano, carboxyl, or formamide. In certain embodiments, R ^4b is hydrogen. In some embodiments, R ^4b is bromo.

For example, both R ^3b and R ^4b are hydrogen. Both R ^3b and R ^4b can be bromo.

In certain embodiments, the presently disclosed embodiments include a compound or

pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the compound having formula (IV):

wherein:

R ^lc is selected from the group consisting of: hydrogen, Ci_6 alkyl, Ci_ ₆ carboxyalkyl, Ci_i2 sulfonyl optionally substituted with 1-6 halo, C6-i ₂ aryl sulfonyl optionally substituted with 1-6 halo and Cz _t _i2 heteroaryl sulfonyl optionally substituted with 1-6 halo;

R ^2c is selected from the group consisting of: hydrogen; hydroxyl; cyano; halo; amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl; and Q_ 12 alkoxyl;

R ^3c is selected from the group consisting of: carboxyl; Ci_ ₆ alkoxycarbonyl; hydroxyl; Ci_i ₂ alkoxyl; cyano; halo; and amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl;

R ^4c is selected from the group consisting of: hydrogen, halo, hydroxyl, and Q_3 alkoxyl; and one or both of Qi and (¾ are nitrogen.

In some embodiments, one or more of the following definitions apply:

(3) R ^2c is hydrogen; hydroxyl; or C1 2 alkoxyl; and/or (4) R ^c is carboxyl; Ci_6 alkoxycarbonyl; hydroxyl; or amine substituted with 1-2 Ci_6 alkyl.

For example, R ^lc can be hydrogen. R ^lc can also be Ci_6 alkyl or C2-6 carboxyalkyl (e.g., - CH ₂ C(0)OH). R ^lc can also be C1 2 sulfonyl optionally substituted with 1-6 halo or e-u aryl sulfonyl (e.g., -S(0)2Ph) optionally substituted with 1-6 alkyl, substituted alkyl (e.g., CF ₃ ) and/or halo. R ^lc can also be C4 2 heteroaryl sulfonyl optionally substituted with 1-6 alkyl, substituted alkyl (e.g., CF ₃ ) and/or halo.

R ^2c can be hydrogen or hydroxyl. R ^2c can also be cyano; halo; or amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _6 alkenyl, C ₃ _ ₆ cycloalkyl, aryl, and/or heteroaryl. R ^c can also be C 1-12 alkoxyl.

R ^3c can be carboxyl or Ci_ ₆ alkoxycarbonyl (e.g., -C(0)OCH ₃ or -C(0)OCH ₂ CH ₃ ). R ^3c can also be hydroxyl. R ^3c can also be alkoxyl; cyano; or halo (e.g., bromo). R ^3c can also be amine optionally substituted with 1 or more Q_6 alkyl, C2-6 alkenyl, C ₃ _6 cycloalkyl, aryl, and/or heteroaryl, such as N(CH ₃ ) ₂ .

R ^4c can be hydrogen or halo (e.g., bromo). R ^4c can also be hydroxyl or and Q_ ₃ alkoxyl.

Qi and Q ₂ can both be nitrogen. Alternatively, one of Qi and Q ₂ is nitrogen and the other of Qi and Q2 is carbon. In some embodiments, when both Qi and Q ₂ are be nitrogen and both R ^2c and R ^3c are hodroxyl, the corresponding ring structure is typically represented by:

In certain embodiments, the presently disclosed embodiments include a compound or pharmaceutically acceptable salt thereof, for promoting neurogenesis and/or reducing neuronal cell death, the

(V)

wherein R ^ld is selected from the group consisting of: hydrogen and CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ - N(R ⁶ )(R ⁷ );

wherein one of R ^A1 and R ^A2 is hydroxyl or halo and the other is hydrogen; and wherein R ⁶ and R ⁷ are each independently selected from the group consisting of:

hydrogen; e-u aryl optionally substituted with 1 or more halo, hydroxyl, Ci_6 alkyl and/or d_6 alkoxyl; and Czt_i ₂ heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or d_6 alkoxyl;

wherein R ^2d is selected from the group consisting of: halo, hydroxyl, C _{1 2} alkoxyl, cyano, aryl, and heteroaryl;

wherein R ^3d is selected from the group consisting of: hydrogen and amine optionally substituted with 1 or more Ci_ ₆ alkyl, C ₂ _ ₆ alkenyl, C ₃ _ ₆ cycloalkyl, C ₂ _ ₆ heterocyclyl, aryl, and/or heteroaryl; and

wherein R ^4d is selected from the group consisting of: hydrogen, halo, hydroxyl, and Ci_ ₃ alkoxyl.

In some embodiments, R ^2d is cyano, and/or R ^4d is hydrogen, bromo or methoxy.

For example, R ^ld can be hydrogen. R ^ld can also be CH ₂ -C(R ^A1 )(R ^A2 )-CH ₂ -N(R ⁶ )(R ⁷ ). One of R ^A1 and R ^A2 can be hydroxyl and the other is hydrogen. One of R ^A1 and R ^A2 can be halo (e.g., fluoro) and the other is hydrogen. Alternatively, both R ^A1 and R^ can be hydrogen. R ⁶ and R ⁷ can both be hydrogen.

Alternatively, one or both of R ⁶ and R ⁷ can be -u aryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or d_6 alkoxyl; or heteroaryl optionally substituted with 1 or more halo, hydroxyl, Q_6 alkyl and/or d_6 alkoxyl.

R ^2d can be halo, hydroxyl, or Ci_i ₂ alkoxyl. R ^2d can also be cyano. R ^2d can also be aryl (e.g., Q-

₁₂ ) or heteroaryl (e.g., C ₄ -i ₂ ).

R ^3d can be hydrogen. R ^3d can also be amine optionally substituted with 1 or more Ci_6 alkyl, C ₂ _6 alkenyl, C ₃ _6 cycloalkyl, C ₂ _6 heterocyclyl, aryl (e.g., Ce-n), and/or heteroaryl (e.g., d_i ₂ ).

_R 4d

can be hydrogen, halo (e.g., bromo), hydroxyl, or Ci_ ₃ alkoxyl (e.g., methoxyl).

Compounds or salts thereof having any combinations of the the above definitions of the various groups are all included in the presently disclosed embodiments.

All publications and patents mentioned herein are hereby incorporated by reference in their entirety as if each individual publication or patent was specifically and individually indicated to be incorporated by reference.