CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority to U.S. Provisional Appl. Ser. No. 62/524,738, filed June 26, 2018, which is incorporated by reference as if fully set forth herein.

BACKGROUND

Diacylglycerols (DAGs) and phosphatidic acid (PA) play roles in biology as basic components of membranes, intermediates in lipid metabolism, and secondary messengers in cellular signaling (Carrasco and Merida, 2007; Fang et al., 2001). Cells regulate intracellular DAG and PA levels through metabolic networks that utilize distinct enzymes to produce or consume these secondary messengers/metabolites (Brown et al., 2017; Carrasco and Merida, 2007; Hsu et al., 2012; Shulga et al., 2011). One such enzymatic pathway of signal transduction is adenosine triphosphate (ATP)-dependent phosphorylation of DAGs to biosynthesize phosphatidic acid (PA) by a set of lipid kinases collectively known as diacylglycerol kinases (Shulga et al., 2011) (DGKs). DAG and PA are lipid messengers that alter localization (Takai et al., 1979), activation (Newton and Koshland, 1989), and protein-protein interactions (Fang et al., 2001) of distinct sets of receptor proteins.

SUMMARY

Provided herein are compounds and uses thereof. For Example, this disclosure relates to at least the following compounds, others disclosed herein and uses thereof:

A compound according to formula (I), formula (II), formula (III), formula (IV), or formula

(V):

(I),

(V),

or a pharmaceutically acceptable salt, polymorph, prodrug, or solvate thereof;

wherein:

X is selected from the group consisting of: -CR ¹⁹ R ¹³ -, -NR ³⁵ -;

Y is selected from the group consisting of: -CR ¹² R ²⁰ -, -NR ³⁶ -;

and X is selected from the group consisting of: I , or I ;

Rl P 2 p 3 p 4 p 5 p 6 p 7 p 8 p 9 n 10 p ll n 12 n 13 n 14 n 15 n 16 n 17 n 18 n 19 p 20 p 21 p 22

_R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 30 _R 31 _R 32 _R 33 _R 34 _R 35 _R 36 _R 37 ^ _R 38 independently, are selected from the group consisting of -H, -F, -CI, -Br and substituted or unsubstituted (C1-C100) hydrocarbyl.

DRAWINGS

FIGs 1A-B. Mammalian diacylglycerol kinase (DGK) superfamily. (A) DGK enzymes catalyze transfer of phosphate from ATP to diacylglycerol (DAG) to biosynthesize phosphatidic acid (PA). The molecular structure of fatty acyl chains regulates functional properties of DAG and PA lipids. (B) The ten DGK isoforms identified to date are divided into five principal subtypes based on organization of structural motifs. Alternative splicing of certain DGK subtypes can generate additional structural diversity. RVH: recoverin homology domain; EF: EF Hands motif; C I :

atypical/typical C I domain; PH: pleckstrin homology domain; SAM: sterile alpha motif; EPAP: Glu- Pro-Ala-Pro repeats (SEQ ID NO: 1); PDZ: protein-protein interactions; HD: hydrophobic domain; MARCKS: myristolated alanine-rich C kinase substrate domain; ANK: Ankyrin repeats; PR: proline- rich region.

FIGs 2A-B. Activity-based probes and inhibitors for functional analysis of DGKs. (A) Chemical structure and mechanism of ATP acyl phosphate probe labeling. The ATP binding group mediates interactions with lipid and protein kinases to place the reactive acyl phosphate group in proximity of lysines in the active site. The side chain amino group of lysine covalently reacts with probe, releasing ATP, and covalently attaches desthiobiotin to kinase through an amide bond. (B) The DGKot inhibitor ritanserin and matching negative control inhibitor ketanserin. FIGs 3A-C. ATP acyl phosphates enable gel-based activity-based profiling of DGKot. (A) In vitro IC50 values for DGKot inhibition by ritanserin as measured by DAG phosphorylation substrate assay described in Figure 9. Data shown are mean +/- SEM. for triplicate measurements. Results are representative of two independent biological replicates. 95% confidence intervals for IC ₅₀ values: 20- 30 μΜ. (B) Gel-based ATP acyl phosphate assay was used to determine in vitro IC ₅₀ values for

DGKot inhibition by ritanserin (95% confidence intervals for IC50 values: 17-192 μΜ). Details of the assay and representative gels used to calculate potency values can be found in Figure 10. (C) DGKot- HEK293T soluble proteomes were pretreated with ritanserin (100 μΜ), ketanserin (100 μΜ), or ATP (1 mM) for 30 min prior to addition of ATP acyl phosphate probe (10 μΜ, 30 min) and gel-based analysis as described in Figure 10. Pretreatment with ritanserin but not ketanserin blocked probe labeling of -80 kDa recombinant DGKot. Western blot analysis (anti-FLAG, 0.8 μg/mL) confirmed equivalent recombinant protein expression across treatment conditions.

FIGs 4A-C. Elucidation of ATP and ligand-binding sites of DGKot by quantitative chemical proteomics. (A) Schematic of quantitative LC-MS proteomics workflow to identify ligand binding sites of recombinant DGKs using ATP acyl phosphate probe. See STAR Methods for more details. (B) Left - MS2 spectra of probe-modified peptides corresponding to the active site of DGKot. Major b- and y-ion fragments derived from neutral losses of the precursor (M) are indicated on spectrum in red. An asterisk denotes fragments containing probe-modified lysine residues corresponding to the red-labeled lysine shown in the peptide sequence. Right - MS I extracted ion chromatograms of probe- modified peptides with corresponding SILAC ratios quantifying vehicle -treated (light): compound- treated (heavy). (C) Schematic of DGKot showing domains where ATP probe binding is detected by quantitative chemical proteomics. Orange circles represent ATP probe binding at K237 of the CI domain, K377 of the DAGKc domain, and K539 of the DAGKa domain. (SEQ ID NOs: 2-4)

FIGs 5A-C. Chemical proteomic profiling of the DGK superfamily. (A) Heatmap showing SILAC ratios for probe-binding sites of respective DGK isoforms in ATP (1 mM, 30 min) - versus

DMSO vehicle -treated recombinant HEK293T proteomes. DGK ATP binding sites are defined by SR > 5. (B-C) Sequence similarity of ATP binding sites of DGK isoforms measured by quantitative proteomics. Multiple sequence alignments of probe-modified peptides were performed using Clustal Omega and results analyzed by sequence logos (See STAR Methods for details) to search for common motifs within the DAGKc (B) and DAGKa (C) ATP-binding sites of DGKs. The height of each stack denotes sequence conservation at the respective position (measured in bits). The height of individual residues within the stack indicates the relative frequency of corresponding amino acids at that position. The numbers in parentheses indicate the number of DGKs that show modification at the respective probe-modified lysine. Color scheme for amino acids in sequence logos is as follows: hydrophilic, blue; neutral, green; hydrophobic, black. Probe modified peptides used for sequence alignment and logo analysis can be found in Figure 13 and Table 1 and 1A.

FIGs 6A-B. Inhibitor profiling of the DGK superfamily. (A) Heat map showing SILAC ratios of DGK probe-binding sites that are competed (SR > 5) with ritanserin- versus DMSO vehicle control-treated samples. Lack of competition at respective sites in ketanserin-treated samples indicates ritanserin competition was specific. (B) Representative extracted ion chromatograms (MS I) of probe modified peptides from DGKa CI and DAGKa domains, which represent the primary sites of binding for ritanserin. Ketanserin is inactive at these same sites. For all studies, proteomes were pretreated with compounds (100 μΜ) for 30 min prior to labeling with ATP acyl phosphate probe (10 μΜ, 30 min).

FIGs 7A-E. Discovery of a lead fragment inhibitor of DGKa by chemical proteomics. (A) Heat map showing potency and selectivity of ritanserin and RF001 against recombinant DGKs and native kinases detected in HEK293T proteomes. (B) Representative extracted ion chromatograms (MS I) of probe modified peptide from FER, showing potent competition with ritanserin but not RFOOl . (C) Ritanserin deconstruction to identify the fragment RFOOl, which shows concentration- dependent blockade of recombinant DGKa as measured by substrate assay (Figure 9). Data shown are mean +/- SEM. for triplicate measurements. Results are representative of two independent biological replicates. 95% confidence intervals for IC50 values: 120-414 μΜ. Dotted line represents background activity detected in non-transfected HEK293T proteomes. (D) Representative extracted ion chromatograms (MSI) showing the primary sites of binding for RFOOl against DGKa. Quantified SILAC ratios shown are averages of two biological replicates. (E) Bar graph comparing the total number of kinase targets (recombinant DGKs and native kinases in HEK293T proteomes) observed with potent (SR > 5), moderate (SR > 3), and weak competition (SR > 2) at respective probe-binding sites in ritanserin- versus RFOOl-treated samples. For quantitative LC-MS experiments, proteomes were pretreated with compounds (100 μΜ) for 30 min prior to labeling with ATP acyl phosphate probe (10 μΜ, 30 min).

FIG 8. Related to Figures 5 - 7. Western blot analysis of recombinant overexpressed DGK isoforms. DGK isoforms were recombinantly expressed in HEK293T cells and proteomes subjected to western blot analysis (anti-FLAG, 0.8 μg/mL; anti-HA, 0.1 μg/mL). Soluble fractions were used for analysis with the exception of epsilon, which is expressed predominantly in the membrane fraction (highlighted by red boxes).

FIGs 9A-B. Related to Figure 3 and 7. Measuring activity and inhibition of recombinant DGKa in HEK293T cells by substrate assay. (A) The ADP-glo assay measures ATP that has been converted to ADP by the action of kinases in the cell lysate though production of luminescent signal in proportion to ADP produced. (B) Production of active recombinant DGKa was determined by enhanced activity in DGKa-HEK293T versus mock-transfected soluble proteomes as measured using ADP-glo assay. The lack of activity with heat-denatured (95° C for 5 min) DGKa-HEK293T proteomes supports that activity was specific for recombinant DGKa. Pretreatment with ritanserin but not ketanserin (100 μΜ compounds) resulted in -80% blockade of recombinant DGKa activity. Data shown are mean + s.e.m. for two independent biological replicates; n = 2 per group. ****p < 0.0001 for mock versus DGKa overexpressed group (DMSO); **P < 0.01, ****p < 0.0001 for vehicle- treated versus heat-denatured or inhibitor-treated DGKa overexpressed groups (DMSO).

FIGs 10A-E. Related to Figure 3. Optimization of gel-based ATP acyl phosphate assay for profiling DGK inhibitors. (A) Schematic of gel-based chemical proteomic analysis of recombinant DGKa activity. DGKa-HEK293T soluble proteomes were labeled with ATP acyl phosphate, proteins separated by SDS-PAGE, transferred to nitrocellulose, and desthiobiotin-modified proteins detected by streptavidin fluorophore and in-blot fluorescence. Pretreatment of proteomes with inhibitors blocks labeling at ATP probe binding sites, resulting in reductions in fluorescence signals to profile on- and off-targets of recombinant DGKa. (B) DGKa-HEK293T soluble proteomes were treated with ATP probe at the indicated concentrations for 30 min, quenched with gel loading buffer, and subjected to gel-based analysis as described above. (C) Integrated band intensities from these studies were plotted as a function of ATP probe concentrations to identify a suitable treatment condition for profiling of reversible inhibitors (10 μΜ ATP probe, 30 min; labeling reaction was -40% complete). (D) DGKa- HEK293T soluble proteomes were pretreated with ritanserin or ketanserin for 30 min at the indicated concentrations followed by ATP probe labeling (10 μΜ, 30 min) and gel-based chemical proteomics analysis as described above. Ritanserin but not ketanserin showed concentration dependent blockade of ATP probe labeling. (E) Pretreatment with the widely used DGK inhibitors R59022 and R59949 (100 μΜ compounds) also blocked DGKa probe labeling as measured by gel-based chemical proteomics. For all chemical proteomics studies, western blots (anti-FLAG, 0.8 μg/mL) were included to confirm that changes in fluorescence were not due to variations in recombinant protein expression (bottom panels).

FIG 11. Related to Figure 4. Proximity of S. aureus DgkB residue, with homology to DGKa K377, to phosphate groups of ADP. Cartoon Diagram of DgkB monomer (PDB code: 2QV7): a helices are cyan, β sheets and loops are grey, ADP is transparent spheres with a stick model, Mg is blue, the aligned region is green and the homologous residue (threonine 12) is depicted as a green stick model. Partial Structure-Aided Sequence Alignment of S. aureus DgkB and rat DGKa: aligned region is green and ATP acyl phosphate probe-modified DGKa residue is red (K377). Note the threonine residue homologous to the probe-modified lysine of DGKa is in proximity to phosphate groups of ADP. (SEQ ID NOs: 5-6)

FIGs 12A-B. Related to Figure 7. Chemical proteomic analysis of RFOOl activity against recombinant DGKa in HEK293T proteomes. (A) DGKa-HEK293T soluble proteomes were pretreated with RFOOl at the indicated concentrations for 30 min prior to labeling with ATP acyl phosphate probe (10 μΜ, 30 min). After probe labeling, proteomes were subjected to gel-based analyses as described in Figure 10A. RF001 blocked probe labeling in a concentration-dependent manner and the decrease in fluorescence signals was not due to differences in recombinant protein expression as confirmed by western blot (bottom panel, anti-FLAG, 0.8 μg/mL). Integrated band intensities from these gel-based ATP acyl phosphate assays (B) were used to quantify DGKa inhibition by RF001. Mock-transfected and heat-denatured (95° C for 2 min) recombinant DGKa lysates were included as additional controls. Data shown are mean + s.e.m. for three biological replicates. **P < 0.01 for mock versus DGKa overexpressed group (0 μΜ); **P < 0.01 for vehicle- treated (0 μΜ) versus heat-denatured or inhibitor-treated DGKa overexpressed groups.

FIG 13. Related to Figure 5. Sequence similarity in ATP binding sites of DGK isoforms.

Multiple sequence alignment of DGK isoforms were performed with Clustal Omega (Goujon et al., 2010; Sievers et al., 2011) and ATP -sensitive probe-modified peptides found in DAGKc and DAGKa subdomains are shown (highlighted by a red box). Site of probe labeling for ATP acyl phosphate is denoted by a red underline. An asterisk denotes single, fully conserved residue; colon denotes indicates conservation between groups of strongly similar properties; a period signifies conservation between groups of weakly similar properties (Goujon et al., 2010; Sievers et al., 2011). (SEQ ID NOs: 7-16)

Table 1 and 1A Related to Figure 4 - 7. SILAC ratios for ATP, Ritanserin, Ketanserin, and RFOOl treatment of recombinant DGK-HEK293T soluble lysates. Multiple sequence alignments for sequence logo analysis.

FIGs 14A-B. Compound and chemical proteomic assays used in cell biology of NSCLC and SCLC cells.

FIGs 15A-B. Ritanserin, and not Ketanserin, inhibits lung cancer cell survival. A) Lung cancer cell viability as determined through the WST-1 assay. Cells were incubated with compound at the given concentrations for two days and then assayed for metabolic activity. Data are from at least two independent biological replicates and significance values are determined by comparison with Ketanserin treatment of the same concentration. All values were normalized to vehicle treatment. B) Timecourse data for 25 μΜ (Ketanserin, Ritanserin) or 1 μΜ (Staurosporine) compound treatment. Cells were plated and mixed with inhibitor on day 0, and assayed for metabolic activity via the WST- 1 assay for four subsequent days. Data are from at least two independent biological replicates performed in triplicate, and signficance values are given with respect to Ketanserin treatment at the same timepoint. All values were normalized to vehicle treatment. *P < 0.05, **P < 0.01, *** P < .001, and ****P < 0.0001.

FIGs 16A-B. Additional measures of cell death. A) Direct counts of cells after 48 hours of compound treatment with either Staurosporin (Staur), Ketanserin (Ket), or Ritanserin (Rit) at the given concentrations. Adherent cells (A549 and H1650) were detached with trypsin and live cells were distinguished through death staining with 10 nM Trypan Blue. All results were normalized to vehicle control (DMSO), which was assigned a value of 1. Significance was calculated by comparison with 10 μΜ Ketanserin treatment. B) Determination of apoptosis via the CaspaseGlo 3/7 assay. Cells were incubated with the compounds at the concentrations given and allowed to grow for 24 hours, at which point caspase activity was measured. Assays were performed in triplicate and are representative of at least two independant biological replicates. Significance was calculated by comparison with vehicle control. *P < 0.05, **P < 0.01, *** P < .001, and ****P < 0.0001.

FIG 17. Kinome target engagement profiles if ritanserin using ATP acyl phosphates.

FIGs 18A-C. Additional time points and cell lines for cell viability study. A and B) Lung cancer cell viability as determined through the WST-1 assay A) 1 day or B) 4 days after addition of compounds. Cells were incubated with compound at the given concentrations for one day and then assayed for metabolic activity. Data are from at least two independent biological replicates performed in triplicate and significance values are determined by comparison with Ketanserin treatment of the same concentration and time point. All values were normalized to vehicle treatment. C) WST-1 Cell Proliferation Assay time course of Bone Marrow Derived Macrophages (BMDMs) treated with either 1 μΜ Staurosporin, 25 μΜ Ritanserin, or 25 μΜ Ketanserin. All values were normalized to vehicle treatment and significance determined with respect to 25 μΜ Ketanserin treatment at the same timepoint. Data are from two independent biological replicates performed in triplicate. * P < 0.05, ** P < 0.01, *** P < .001, and **** P < 0.0001.

FIG 19. Quantitative chemical proteomics using SILAC.

FIGs 20A-I. CRAF response to ritanserin (Rit) and RFOOl, and CHK2 response to RFOOl treatments. A-B) SILAC peaks of CRAF ATP Acyl -phosphate labeling in Heavy samples in vitro treated with 1 mM RFOOl or DMSO in (A) H82 Small Cell Lung Cancer Cell and (B) HEK293T cell lysates. C) Ratio of CRAF ATP Acyl -phosphate labeling peptide intensity for heavy labeled compound treated (H) over light labeled DMSO control (L) in H82 and HEK293T cell lines. D-E) SILAC peaks of CRAF ATP Acyl -phosphate labeling in Heavy samples in vitro treated with 100 uM Rit or DMSO in (D) H82 Small Cell Lung Cancer Cell Line and (E) HEK293T cells. F) Ratio of CRAF ATP Acyl-phosphate labeling peptide intensity for heavy labeled compound treated (H) over light labeled DMSO control (L) in H82 and HEK293T cell lines. G-I) SILAC peaks of CHK2 ATP Acyl-phosphate labeling in Heavy samples in vitro treated with 1 mM RFOOl or DMSO in (G) H82 and (H) HEK293T cells. I) Ratio of CHK2 ATP Acyl-phosphate labeling peptide intensity for heavy labeled compound treated (H) over light labeled DMSO control (L) in H82 and HEK293T cell lines. DESCRIPTION

Diacylglycerol kinases (DGKs) are components of signal transduction cascades that regulate cell biology through ATP-dependent phosphorylation of the lipid messenger diacylglycerol. Methods for direct evaluation of DGK activity in native biological systems are lacking and needed to study isoform -specific functions of these multidomain lipid kinases. Here, ATP acyl phosphate activity- based probes and quantitative mass spectrometry were used to define, for the first time, ATP- and small molecule-binding motifs of representative members from all five DGK subtypes. Chemical proteomics was used to discover an unusual binding mode for the DGK-alpha (DGKa) inhibitor ritanserin, including interactions at the atypical CI domain distinct from the ATP binding region. Unexpectedly, deconstruction of ritanserin yielded a fragment compound that blocks DGKa activity through a conserved binding mode and enhanced selectivity against the kinome. Collectively, the studies illustrate the power of chemical proteomics to profile protein-small molecule interactions of lipid kinases for fragment-based lead discovery.

The disclosure relates to compounds of the formula (la):

(la)

or a pharmaceutically acceptable salt, polymorph, prodrug, or solvate thereof;

wherein:

Pvi and P2, independently, are F, CI, Br, CH ₃ , CF ₃ , OCF ₃ , OCH ₃ , CH ₂ F, NH ₂ ,

NHS0 ₂ CH ₂ CH ₂ CH ₃ , CONHCH ₃ , C(CH ₃ ) ₃ , NHCH(CH ₃ ) ₂ , CH ₂ OH, COC ₅ HnN, COOH, or OH;

R ₃ is F, CI, Br, CH ₃ , CF ₃ , OCF ₃ , OCH ₃ , CH ₂ F, NH ₂ , NHS0 ₂ CH ₂ CH ₂ CH ₃ , CONHCH ₃ , C(CH ₃ ) ₃ , NHCH(CH ₃ ) ₂ , CH ₂ OH, COC ₅ HnN, COOH, OH,

10

11

(ritanserin).

ents, the compound is not ritanserin.





or a pharmaceutically acceptable salt, polymorph, prodrug, or solvate thereof;

wherein:

X is selected from the group consisting of: -CR ¹⁹ R ¹³ -, -NR ³⁵ -;

Y is selected from the group consisting of: -CR ¹² R ²⁰ -, -NR ³⁶ -;

and X is selected from the group consisting of: I , or I ;

Rl P2 p3 p4 p5 p6 p7 p8 p9 n 10 p ll n 12 n 13 n 14 n 15 n 16 n 17 n 18 n 19 p20 p21 p22

_R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 30 _R 31 _R 32 _R 33 _R 34 _R 35 _R 36 _R 37 ^ _R 38 independently, are selected from the group consisting of -H, -F, -CI, -Br and substituted or unsubstituted (C1-C100) hydrocarbyl.

In one embodiment, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , _R i9 _R 2o _R 2i _R 22 _R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 3o _R 3i _R 32 _R 33 _{and R} 34 independently, are selected from the group consisting of: substituted or unsubstituted (Ci-Cioo)alkyl, (Ci-Cioo)alkenyl, (Ci-Cioo)alkynyl, (Ci-Cioo)acyl, (C ₃ -C ₂ o)cycloalkyl, (Ci-C ₂ o)aryl, (Ci-C ₂ o)aralkly, (Ci-Cioo)alkoxy, an amine, or (Ci-Cioo)haloalkyl.

In another embodiment, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ , R ¹⁶ , R ¹⁷ ,

_R 18 _R 19 _R 20 _R 21 _R 22 _R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 30 _R 31 _R 32 _R 33 _R 34 _i ndependently, are selected from the group consisting of: substituted or unsubstituted (Ci-C4o)alkyl, (Ci-C4o)alkenyl, (Ci-C4o)alkynyl, (Ci-C4o)acyl, (C3-Cio)cycloalkyl, (Ci-Cio)aryl, (Ci-Cio)aralkly, (Ci-C4o)alkoxy, an amine, or (Ci-C4o)haloalkyl.

In embodiment, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ , R ¹⁶ , R ¹⁷ , R ¹⁸ , R ¹⁹ , _R 2o _R 2i _R 22 _R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 3o _R 3i _R 32 _R 33 _{md R} 34 independently, are selected from the group consisting of: -F, -CI, -Br, -CH3, -CF3, -OCF3, -OCH3, -CH2F, -NH2, - NHSO2CH2CH2CH3, -CONHCH3, -C(CH ₃ ) ₃ , -NHCH(CH ₃ ) ₂ , -CH ₂ OH, -COC ₅ HnN, -COOH, -OH,



 Formula I

. is independently H, halogen, -CN, -NH

θαϋΠ 2, -NH(alkyl), -N(alkyl) ₂ , -OH, -C(=0)OH,

-C(=0)0(alkyl), -C(=0)NH

-C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl), -S(=0)

₂ N(alkyl)2. -CF ₃ , alkyl which is optionally substituted, alkoxy which is optionally substituted

. is independently H, halogen, -CN, -NH

each R ² ^ ^{J a} , -NH(alkyl) -N(alkyl), -OH -C(=0)OH

-C(=0)0(alkyl), -C(=0)NH ² ' ^{Ι Π} ^»'>· '^' Τ'Λ. ^

-i>(-u) aikyi which is optionally substituted, alkoxy which is optionally substituted

2N(alkyl)2> - r ₃

m is 1 ,2,3,4, or 5

n is 1 ,2,3,4, or 5

is selected from

R ³

Formula II

is independently H, halogen, -CN, -NH

e- ^a c ^C ( ^h =0 ^R )0(a, _k yl) -C(=0)NH * ^" ^'^' ^" ^'^' ^" OH. -C(=0)OH,

-S(=0) 2, -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

2N(alkyl)2. " ^CF 3. ^3| which is optionally substituted, alkoxy which is optionally substituted

, is independently H, halogen, -CN, -NH

e-C ^C ( ^h =0 ^R )0(a,kyl) -C(=0)NH ^" ° ^Η ' - ^C(= ° ^)OH '

-S(=0) ₂ , -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

2N(alkyl)2. ^_CF 3. ^alk y! which is optionally substituted, alkoxy which is optionally substituted o is 1 ,2,3,4, or 5

p is 1 ,2,3,4, or 5

_ - is selected from

R ⁶ F

. is independently H, halogen, -CN, -NH

each R ⁷ ^ ' ' ^a ' ' -NH(alkyl) -N(alkyl), -OH -C(=0)OH

-C(=0)0(alkyl), -C(=0)NH ² ' ' ^Π ^»' '^ ^d "^2.

-S(=0) 2. -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

2N(alkyl)2. -CF ₃ , alkyi which is optionally substituted, alkoxy which is optionally s ^ub alogen, -CN, -NH

each ^ti i RM ⁸ , ^t ¾ ⁱ independently H, h

^ _? , -NH(alkyl), -N(alkylW -OH, -C(=0)OH,

-C(=0)0(alkyl), -C(=0)NH ² ' ^{y y} ' ² ' ' ' '

-S(=0) ₂ , -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

₂ N(alkyl)2 _> -CF ₃ , alkyi which is optionally substituted, alkoxy which is optionally substituted

q is 1 ,2,3,4, or 5

r is 1 ,2,3,4, or 5

„ is selected from

R ⁹

Consolidated Formula

. is independently H, halogen, -CN, -NH

e -aCc(h=0 R) ¹ 0(alkyl) ^, -C(=0)N ^J H ^a , ² ' -N ^Ι H ^Π (^alky»l')>· -N(alkyl), -O ^H ^"i , -C ^(=0),OHn,

-S(=0) ₂ , -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

₂ N(alkyl)2. -CF ₃ , alkyi which is optionally substituted, alkoxy which is optionally substituted

. _ is independently H, halogen, -CN, -NH

each R ² ^ ^J ' ^a ' ' , -NH(alkyl) -N(alkyl), -OH -C(=0)OH

-C(=0)0(alkyl), -C(=0)NH ² ' ^{Ι Π} ^»'>· ^n, ^ , n,

-S(=0) ₂ , -C(=0)NH(alkyl), -C(=0)N(alkyl) ₂ , -S(=0) ₂ NH ₂ , -S(=0) ₂ NH(alkyl),

2N(alkyl)2. -CF ₃ , alkyi which is optionally substituted, alkoxy which is optionally substituted m is 1 ,2,3,4, or 5

n is 1 ,2,3,4, or 5

A is selected from C, CH, or

N

B is selected from C, CH, or C(OH),

, is selected from

R ³



ID

100 UM

1 mM ¾ Reference Reference Molecular

Name Stru tu re

Activity sheet sheet Mass

Activity

ΤΗ032 180413 94 180413 399.53

ΤΗ033 180413 72 180413 .617.75

180501 180501

THQ35 ₄ 0

Alpha Alpha

180501 180501

ΤΗ036 74 93

Alpha Alpha

W

00

The present disclosure also contemplates pharmaceutical compositions comprising one or more compounds of the formula (IA), (I)-(V), one or more pharmaceutically acceptable carriers, diluents, excipients or combinations thereof. A "pharmaceutical composition" refers to a chemical or biological composition suitable for administration to a subject (e.g., mammal). Such compositions can be specifically formulated for administration via one or more of a number of routes, including but not limited to buccal, cutaneous, epicutaneous, epidural, infusion, inhalation, intraarterial, intracardial, intracerebroventricular, intradermal, intramuscular, intranasal, intraocular, intraperitoneal, intraspinal, intrathecal, intravenous, oral, parenteral, pulmonary, rectally via an enema or suppository, subcutaneous, subdermal, sublingual, transdermal, and transmucosal. In addition, administration can by means of capsule, drops, foams, gel, gum, injection, liquid, patch, pill, porous pouch, powder, tablet, or other suitable means of administration.

A "pharmaceutical excipient" or a "pharmaceutically acceptable excipient" comprises a carrier, sometimes a liquid, in which an active therapeutic agent is formulated. The excipient generally does not provide any pharmacological activity to the formulation, though it may provide chemical and/or biological stability, and release characteristics. Examples of suitable formulations can be found, for example, in Remington, The Science And Practice of Pharmacy, 20th Edition, (Gennaro, A. Pv., Chief Editor), Philadelphia College of Pharmacy and Science, 2000, which is incorporated by reference in its entirety.

As used herein "pharmaceutically acceptable carrier" or "excipient" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents that are physiologically compatible. The carrier is suitable for, among other applications, parenteral administration. Alternatively, the carrier can be suitable for intravenous, intraperitoneal, intramuscular, sublingual, or oral administration. Pharmaceutically acceptable carriers include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the pharmaceutical compositions is contemplated. Supplementary active compounds can also be incorporated into the compositions.

Pharmaceutical compositions can be sterile and stable under the conditions of manufacture and storage. The composition can be formulated as a solution, microemulsion, liposome, or other ordered structure suitable to high drug concentration. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.

In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, or sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, monostearate salts and gelatin. Moreover, the compounds described herein can be formulated in a time release formulation, for example in a composition that includes a slow release polymer. The active compounds can be prepared with carriers that will protect the compound against rapid release, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, polylactic acid and polylactic, polyglycolic copolymers (PLG). Many methods for the preparation of such formulations are known to those skilled in the art.

Oral forms of administration are also contemplated herein. The pharmaceutical compositions can be orally administered as a capsule (hard or soft), tablet (film coated, enteric coated or uncoated), powder or granules (coated or uncoated) or liquid (solution or suspension). The formulations can be conveniently prepared by any of the methods well-known in the art. The pharmaceutical compositions can include one or more suitable production aids or excipients including fillers, binders, disintegrants, lubricants, diluents, flow agents, buffering agents, moistening agents, preservatives, colorants, sweeteners, flavors, and pharmaceutically compatible carriers.

The compounds can be administered by a variety of dosage forms as known in the art. Any biologically-acceptable dosage form known to persons of ordinary skill in the art, and combinations thereof, are contemplated. Examples of such dosage forms include, without limitation, chewable tablets, quick dissolve tablets, effervescent tablets, reconstitutable powders, elixirs, liquids, solutions, suspensions, emulsions, tablets, multi-layer tablets, bi-layer tablets, capsules, soft gelatin capsules, hard gelatin capsules, caplets, lozenges, chewable lozenges, beads, powders, gum, granules, particles, microparticles, dispersible granules, cachets, douches, suppositories, creams, topicals, inhalants, aerosol inhalants, patches, particle inhalants, implants, depot implants, ingestibles, injectables (including subcutaneous, intramuscular, intravenous, and intradermal), infusions, and combinations thereof.

Other compounds which can be included by admixture are, for example, medically inert ingredients (e.g., solid and liquid diluent), such as lactose, dextrosesaccharose, cellulose, starch or calcium phosphate for tablets or capsules, olive oil or ethyl oleate for soft capsules and water or vegetable oil for suspensions or emulsions; lubricating agents such as silica, talc, stearic acid, magnesium or calcium stearate and/or polyethylene glycols; gelling agents such as colloidal clays; thickening agents such as gum tragacanth or sodium alginate, binding agents such as starches, arabic gums, gelatin, methylcellulose, carboxymethylcellulose or polyvinylpyrrolidone; disintegrating agents such as starch, alginic acid, alginates or sodium starch glycolate; effervescing mixtures; dyestuff; sweeteners; wetting agents such as lecithin, polysorbates or laurylsulphates; and other therapeutically acceptable accessory ingredients, such as humectants, preservatives, buffers and antioxidants, which are known additives for such formulations. Liquid dispersions for oral administration can be syrups, emulsions, solutions, or suspensions. The syrups can contain as a carrier, for example, saccharose or saccharose with glycerol and/or mannitol and/or sorbitol. The suspensions and the emulsions can contain a carrier, for example a natural gum, agar, sodium alginate, pectin, methylcellulose, carboxymethylcellulose, or polyvinyl alcohol.

The amount of active compound in a therapeutic composition can vary according to factors such as the disease state, age, gender, weight, patient history, risk factors, predisposition to disease, administration route, pre-existing treatment regime (e.g., possible interactions with other

medications), and weight of the individual. Dosage regimens can be adjusted to provide the optimum therapeutic response. For example, a single bolus can be administered, several divided doses can be administered over time, or the dose can be proportionally reduced or increased as indicated by the exigencies of therapeutic situation.

"Dosage unit form," as used herein, refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms are dictated by and can be directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in individuals. In therapeutic use for treatment of conditions in mammals (e.g., humans) for which the compounds disclosed herein or an appropriate pharmaceutical composition thereof are effective, the compounds disclosed herein can be administered in an effective amount. The dosages as suitable for this disclosure can be a composition, a pharmaceutical composition or any other compositions described herein.

The dosage can be administered once, twice, or thrice a day, although more frequent dosing intervals are possible. The dosage can be administered every day, every 2 days, every 3 days, every 4 days, every 5 days, every 6 days, and/or every 7 days (once a week). The dosage can be administered daily for up to and including 30 days, preferably between 7-10 days. Or the dosage can be administered twice a day for 10 days. If the patient requires treatment for a chronic disease or condition, the dosage can be administered for as long as signs and/or symptoms persist. The patient may require "maintenance treatment" where the patient is receiving dosages every day for months, years, or the remainder of their lives. In addition, the composition can affect prophylaxis of recurring symptoms. For example, the dosage can be administered once or twice a day to prevent the onset of symptoms in patients at risk, especially for asymptomatic patients.

The compositions described herein can be administered in any of the following routes: buccal, epicutaneous, epidural, infusion, inhalation, intraarterial, intracardial, intracerebroventricular, intradermal, intramuscular, intranasal, intraocular, intraperitoneal, intraspinal, intrathecal, intravenous, oral, parenteral, pulmonary, rectally via an enema or suppository, subcutaneous, subdermal, sublingual, transdermal, and transmucosal. The administration can be local, where the composition is administered directly, close to, in the locality, near, at, about, or in the vicinity of, the site(s) of disease, e.g., inflammation, or systemic, wherein the composition is given to the patient and passes through the body widely, thereby reaching the site(s) of disease. Local administration can be administration to the cell, tissue, organ, and/or organ system, which encompasses and/or is affected by the disease, and/or where the disease signs and/or symptoms are active or are likely to occur.

Administration can be topical with a local effect, composition is applied directly where its action is desired. Administration can be enteral wherein the desired effect is systemic (non-local), composition is given via the digestive tract. Administration can be parenteral, where the desired effect is systemic, composition is given by other routes than the digestive tract.

Also contemplated herein are compositions comprising a therapeutically effective amount of one or more compounds that are useful in a method for treating various cancers including small-cell lung cancer and non-small cell lung cancer. [00048] The methods and compositions described herein can be used to treat a variety of cancers and tumors, for example, leukemia, sarcoma, osteosarcoma, lymphomas, melanoma, glioma, pheochromocytoma, hepatoma, ovarian cancer, skin cancer, testicular cancer, gastric cancer, pancreatic cancer, renal cancer, breast cancer, prostate cancer, colorectal cancer, cancer of head and neck, brain cancer, esophageal cancer, bladder cancer, adrenal cortical cancer, lung cancer, bronchus cancer, endometrial cancer, nasopharyngeal cancer, cervical or liver cancer, and cancer at an unknown primary site.

Also contemplated herein are compositions comprising a therapeutically effective amount of one or more compounds of formula (1A), (I), (II), (III), (IV) and/or (V) that are useful in a method for treating various neuropsychiatric disorders, such as, but not limited to, bipolar disorder, depression, schizophrenia, obsessive-compulsive disorder.

Also contemplated herein are compositions comprising a therapeutically effective amount of one or more compounds of formula (1A), (I), (II), (III), (IV) and/or (V) that are useful in a method for treating various neurodegenerative diseases, such as, but not limited to, multiple sclerosis, autistic spectrum disorder, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, Huntington's Disease, Guillain-Barre syndrome, myasthenia gravis, and chronic idiopathic demyelinating disease (CID).

Also contemplated herein are compositions comprising a therapeutically effective amount of one or more compounds of formula (1A), (I), (II), (III), (IV) and/or (V) that are useful in a method for activating T-cells comprising contacting a T cell, such as an inactive T cell, in vitro or in vivo, with an effective amount of one or more compounds of formula (1A), (I), (II), (III), (IV) and/or (V).

Also contemplated herein are compositions comprising an effective amount of one or more compounds of formula (1A), (I), (II), (III), (IV) and/or (V) that are useful to inhibit a kinase comprising contacting the kinase with at least one compound of formula (IA), (I), (II), (III), (IV), or (V) or the pharmaceutical composition. In one embodiment, the kinase comprises a regulatory domain, such as a CI domain, and a kinase domain in the same protein. In one embodiment, the kinase is selected from the following:

Uniprot Gene Name

094806 KPCD3 HUMAN Serine/threonine-protein kinase D3

P05129 KPCG HUMAN Protein kinase C gamma type

P41743 KPCI HUMAN Protein kinase C iota type

RAF proto-oncogene serine/threonine-protein

P04049 RAF 1 HUMAN kinase

Q9NS23 RASF1 HUMAN Ras association domain-containing protein 1

Q8WWW0 RASF5 HUMAN Ras association domain-containing protein 5

Q52LW3 RHG29 HUMAN Rho GTPase -activating protein 29

Q13464 ROCK 1 HUMAN Rho -associated protein kinase 1

075116 ROCK2 HUMAN Rho -associated protein kinase 2

Q9H0H5 RGAP1 HUMAN Rac GTPase -activating protein 1

Q12802 AKP 13 HUMAN A-kinase anchor protein 13

Q5VT25 MRCKA HUMAN Serine/threonine-protein kinase MRCK alpha

Pleckstrin homology domain -containing family

Q9Y4G2 PKHMl HUMAN M member 1

Q8NEN9 PDZD8 HUMAN PDZ domain-containing protein 8

Q13459 MY09B HUMAN Unconventional myosin-IXb

Q6DT37 MRCKG HUMAN Serine/threonine-protein kinase MRCK gamma

Q9Y5S2 MRCKB HUMAN Serine/threonine-protein kinase MRCK beta

B2RTY4 MY09A HUMAN Unconventional myosin-IXa

Q15139 KPCD1 HUMAN Serine/threonine-protein kinase Dl

Q9BZL6 KPCD2 HUMAN Serine/threonine-protein kinase D2

Q05655 KPCD HUMAN Protein kinase C delta type

SH3 and cysteine -rich domain-containing

Q99469 STAC HUMAN protein

SH3 and cysteine -rich domain-containing

Q96MF2 STAC3 HUMAN protein 3

SH3 and cysteine -rich domain-containing

Q6ZMT1 STAC2 HUMAN protein 2

P52735 VAV2 HUMAN Guanine nucleotide exchange factor VAV2

Q9UKW4 VAV3 HUMAN Guanine nucleotide exchange factor VAV3

Q9UPW8 UN 13 A_HUMAN Protein unc-13 homolog A

Q8NB66 UN 13C HUMAN Protein unc-13 homolog C Uniprot Gene Name

UN 13B HUMAN

Protein unc-13

014795 homolog B

Q63HR2 TNS2 HUMAN Tensin-2

P15498 VAV HUMAN Proto-oncogene vav

The term "therapeutically effective amount" as used herein, refers to that amount of one or more compounds of the formula (1A), (I), (II), (III), (IV) and/or (V) that elicits a biological or medicinal response in a tissue system, animal or human, that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease or disorder being treated. The therapeutically effective amount can be that which may treat or alleviate the disease or symptoms of the disease at a reasonable benefit/risk ratio applicable to any medical treatment. However, it is to be understood that the total daily usage of the compounds and compositions described herein can be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically-effective dose level for any particular patient will depend upon a variety of factors, including the condition being treated and the severity of the condition; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, gender and diet of the patient: the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidentally with the specific compound employed; and like factors well known to the researcher, veterinarian, medical doctor or other clinician. It is also appreciated that the therapeutically effective amount can be selected with reference to any toxicity, or other undesirable side effect, that might occur during administration of one or more of the compounds described herein.

The present disclosure also contemplates compounds of the formula (IA), (I)-(V) having a activity EC50 value of less than 250 μΜ, less than 150 μΜ, less than 100 μΜ, less than 50 μΜ, less than 25 μΜ, less than 10 μΜ, less than 1 μΜ, less than 500 nM; or from about 1 nM to about 1 μΜ, about 1 μΜ to about 50 μΜ, about 1 μΜ to about 20 μΜ, about 1 nM to about 200 nM, about 50 nM to about 500 nM or about 10 nM to about 150 nM.

The present disclosure also contemplates compounds of the formula (IA), (I)-(V) having a % inhibition of at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 99%; or about 20% to about 100%, about 30% to about 90%, about 40% to about 95%, about 50% to about 90% or about 70% to about 95%. The present disclosure also contemplates compounds of the formula (IA), (I)-(V) having a combination of the two of the aforementioned EC50 values and % inhibition.

Values expressed in a range format should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range were explicitly recited. For example, a range of "about 0.1% to about 5%" or "about 0.1% to 5%" should be interpreted to include not just about 0.1% to about 5%, but also the individual values (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.1% to 0.5%, l . l% to 2.2%, 3.3% to 4.4%) within the indicated range. The statement "about X to Y" has the same meaning as "about X to about Y," unless indicated otherwise. Likewise, the statement "about X, Y, or about Z" has the same meaning as "about X, about Y, or about Z," unless indicated otherwise.

In this document, the terms "a," "an," or "the" are used to include one or more than one unless the context clearly dictates otherwise. The term "or" is used to refer to a nonexclusive "or" unless otherwise indicated. In addition, it is to be understood that the phraseology or terminology employed herein, and not otherwise defined, is for the purpose of description only and not of limitation. Any use of section headings is intended to aid reading of the document and is not to be interpreted as limiting. Further, information that is relevant to a section heading may occur within or outside of that particular section. Furthermore, all publications, patents, and patent documents referred to in this document are incorporated by reference herein in their entirety, as though individually incorporated by reference.

In the methods described herein, the steps can be carried out in any order without departing from the spirit of this disclosure, except when a temporal or operational sequence is explicitly recited. Furthermore, specified steps can be carried out concurrently unless explicit claim language recites that they be carried out separately. For example, a claimed step of doing X and a claimed step of doing Y can be conducted simultaneously within a single operation, and the resulting process will fall within the literal scope of the claimed process.

The term "about" as used herein can allow for a degree of variability in a value or range, for example, within 10%, within 5%, or within 1% of a stated value or of a stated limit of a range.

The term "substituted" as used herein in conjunction with a molecule or an organic group as defined herein refers to the state in which one or more hydrogen atoms contained therein are replaced by one or more non-hydrogen atoms. The term "functional group" or "substituent" as used herein refers to a group that can be or is substituted onto a molecule or onto an organic group. Examples of substituents or functional groups include, but are not limited to, a halogen (e.g., F, CI, Br, and I); an oxygen atom in groups such as hydroxy groups, alkoxy groups, aryloxy groups, aralkyloxy groups, oxo(carbonyl) groups, carboxyl groups including carboxylic acids, carboxylates, and carboxylate esters; a sulfur atom in groups such as thiol groups, alkyl and aryl sulfide groups, sulfoxide groups, sulfone groups, sulfonyl groups, and sulfonamide groups; a nitrogen atom in groups such as amines, hydroxyamines, nitriles, nitro groups, N-oxides, hydrazides, azides, and enamines; and other heteroatoms in various other groups. Non-limiting examples of substituents that can be bonded to a substituted carbon (or other) atom include F, CI, Br, I, OR, OC(0)N(R) ₂ , CN, NO, N0 ₂ , ON0 ₂ , azido, CF ₃ , OCF ₃ , R, O (oxo), S (thiono), C(O), S(O), methylenedioxy, ethylenedioxy, N(R) ₂ , SR, SOR, S0 ₂ R, S0 ₂ N(R) ₂ , S0 ₃ R, C(0)R, C(0)C(0)R, C(0)CH ₂ C(0)R, C(S)R, C(0)OR, OC(0)R,

C(0)N(R) ₂ , OC(0)N(R) ₂ , C(S)N(R) ₂ , (CH ₂ ) ₀ - ₂ N(R)C(O)R, (CH ₂ ) ₀ - ₂ N(R)N(R) ₂ , N(R)N(R)C(0)R, N(R)N(R)C(0)OR, N(R)N(R)CON(R) ₂ , N(R)S0 ₂ R, N(R)S0 ₂ N(R) ₂ , N(R)C(0)OR, N(R)C(0)R, N(R)C(S)R, N(R)C(0)N(R) ₂ , N(R)C(S)N(R) ₂ , N(COR)COR, N(OR)R, C(=NH)N(R) ₂ , C(0)N(OR)R, and C(=NOR)R, wherein R can be hydrogen or a carbon-based moiety; for example, R can be hydrogen, (Ci-Cioo)hydrocarbyl, alkyl, acyl, cycloalkyl, aryl, aralkyl, heterocyclyl, heteroaryl, or heteroarylalkyl; or wherein two R groups bonded to a nitrogen atom or to adjacent nitrogen atoms can together with the nitrogen atom or atoms form a heterocyclyl.

The term "alkyl" as used herein refers to straight chain and branched alkyl groups and cycloalkyl groups having from 1 to 40 carbon atoms, 1 to about 20 carbon atoms, 1 to 12 carbons or, in some embodiments, from 1 to 8 carbon atoms. Examples of straight chain alkyl groups include those with from 1 to 8 carbon atoms such as methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n- heptyl, and n-octyl groups. Examples of branched alkyl groups include, but are not limited to, isopropyl, iso-butyl, sec-butyl, t-butyl, neopentyl, isopentyl, and 2,2-dimethylpropyl groups. As used herein, the term "alkyl" encompasses n-alkyl, isoalkyl, and anteisoalkyl groups as well as other branched chain forms of alkyl. Representative substituted alkyl groups can be substituted one or more times with any of the groups listed herein, for example, amino, hydroxy, cyano, carboxy, nitro, thio, alkoxy, and halogen groups.

The term "alkenyl" as used herein refers to straight and branched chain and cyclic alkyl groups as defined herein, except that at least one double bond exists between two carbon atoms. Thus, alkenyl groups have from 2 to 40 carbon atoms, or 2 to about 20 carbon atoms, or 2 to 12 carbon atoms or, in some embodiments, from 2 to 8 carbon atoms. Examples include, but are not limited to vinyl, -CH=CH(CH ₃ ), -CH=C(CH ₃ ) ₂ , -C(CH ₃ )=CH ₂ , -C(CH ₃ )=CH(CH ₃ ), - C(CH ₂ CH ₃ )=CH ₂ , cyclohexenyl, cyclopentenyl, cyclohexadienyl, butadienyl, pentadienyl, and hexadienyl among others.

The term "organic group" as used herein refers to any carbon-containing functional group. Examples can include an oxygen-containing group such as an alkoxy group, aryloxy group, aralkyloxy group, oxo(carbonyl) group; a carboxyl group including a carboxylic acid, carboxylate, and a carboxylate ester; a sulfur-containing group such as an alkyl and aryl sulfide group; and other heteroatom-containing groups. Non-limiting examples of organic groups include OR, OOR,

OC(0)N(R) ₂ , CN, CF ₃ , OCF ₃ , R, C(O), methylenedioxy, ethylenedioxy, N(R) ₂ , SR, SOR, S0 ₂ R, S0 ₂ N(R) ₂ , S0 ₃ R, C(0)R, C(0)C(0)R, C(0)CH ₂ C(0)R, C(S)R, C(0)OR, OC(0)R, C(0)N(R) ₂ , OC(0)N(R) ₂ , C(S)N(R) ₂ , (CH ₂ )o- ₂ N(R)C(0)R, (CH ₂ ) ₀ - ₂ N(R)N(R) ₂ , N(R)N(R)C(0)R,

N(R)N(R)C(0)OR, N(R)N(R)CON(R) ₂ , N(R)S0 ₂ R, N(R)S0 ₂ N(R) ₂ , N(R)C(0)OR, N(R)C(0)R, N(R)C(S)R, N(R)C(0)N(R) ₂ , N(R)C(S)N(R) ₂ , N(COR)COR, N(OR)R, C(=NH)N(R) ₂ , C(0)N(OR)R, C(=NOR)R, and substituted or unsubstituted (Ci-Cioo)hydrocarbyl, wherein R can be hydrogen (in examples that include other carbon atoms) or a carbon-based moiety, and wherein the carbon-based moiety can be substituted or unsubstituted.

The term "alkynyl" as used herein refers to straight and branched chain alkyl groups, except that at least one triple bond exists between two carbon atoms. Thus, alkynyl groups have from 2 to 40 carbon atoms, 2 to about 20 carbon atoms, or from 2 to 12 carbons or, in some embodiments, from 2 to 8 carbon atoms. Examples include, but are not limited to -C≡CH, -C≡C(CH ₃ ), - C≡C(CH ₂ CH ₃ ), -CH ₂ C≡CH, -CH ₂ C≡C(CH ₃ ), and -CH ₂ C≡C(CH ₂ CH ₃ ) among others.

As used herein, the term "alkynylenyl" broadly refers to substituted or unsubstituted divalent straight chain and branched alkynylenyl groups having from 1 to 40 carbon atoms (C1-C40), from 1 to about 20 carbon atoms (Ci-C ₂ o), from 1 to 12 carbons (Ci-Ci ₂ ), from 1 to 8 carbon atoms (Ci-Cs), or, in some examples, from 1 to 6 carbon atoms (Ci-Ce). Examples of straight chain divalent alkynylenyl groups include those with from 1 to 8 carbon atoms such as ethynyl (-C≡C-CH ₂ -), n-propynyl (-C≡C- CH ₂ -), and the like.

The term "cycloalkyl" as used herein refers to cyclic alkyl groups such as, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl groups. In some embodiments, the cycloalkyl group can have 3 to about 8-12 ring members, whereas in other embodiments the number of ring carbon atoms range from 3 to 4, 5, 6, or 7. Cycloalkyl groups further include polycyclic cycloalkyl groups such as, but not limited to, norbornyl, adamantyl, bornyl, camphenyl, isocamphenyl, and carenyl groups, and fused rings such as, but not limited to, decalinyl, and the like. Cycloalkyl groups also include rings that are substituted with straight or branched chain alkyl groups as defined herein. Representative substituted cycloalkyl groups can be mono-substituted or substituted more than once, such as, but not limited to, 2,2-, 2,3-, 2,4- 2,5- or 2,6-disubstituted cyclohexyl groups or mono-, di- or tri-substituted norbornyl or cycloheptyl groups, which can be substituted with, for example, amino, hydroxy, cyano, carboxy, nitro, thio, alkoxy, and halogen groups. The term "cycloalkenyl" alone or in combination denotes a cyclic alkenyl group.

The term "acyl" as used herein refers to a group containing a carbonyl moiety wherein the group is bonded via the carbonyl carbon atom. The carbonyl carbon atom is bonded to a hydrogen forming a "formyl" group or is bonded to another carbon atom, which can be part of an alkyl, aryl, aralkyl cycloalkyl, cycloalkylalkyl, heterocyclyl, heterocyclylalkyl, heteroaryl, heteroarylalkyl group or the like. An acyl group can include 0 to about 12, 0 to about 20, or 0 to about 40 additional carbon atoms bonded to the carbonyl group. An acyl group can include double or triple bonds within the meaning herein. An acryloyl group is an example of an acyl group. An acyl group can also include heteroatoms within the meaning herein. A nicotinoyl group (pyridyl-3-carbonyl) is an example of an acyl group within the meaning herein. Other examples include acetyl, benzoyl, phenylacetyl, pyridylacetyl, cinnamoyl, and acryloyl groups and the like. When the group containing the carbon atom that is bonded to the carbonyl carbon atom contains a halogen, the group is termed a "haloacyl" group. An example is a trifluoroacetyl group.

The term "aryl" as used herein refers to cyclic aromatic hydrocarbon groups that do not contain heteroatoms in the ring. Thus, aryl groups include, but are not limited to, phenyl, azulenyl, heptalenyl, biphenyl, indacenyl, fluorenyl, phenanthrenyl, triphenylenyl, pyrenyl, naphthacenyl, chrysenyl, biphenylenyl, anthracenyl, and naphthyl groups. In some embodiments, aryl groups contain about 6 to about 14 carbons in the ring portions of the groups. Aryl groups can be unsubstituted or substituted, as defined herein. Representative substituted aryl groups can be mono-substituted or substituted more than once, such as, but not limited to, a phenyl group substituted at any one or more of 2-, 3-, 4-, 5-, or 6-positions of the phenyl ring, or a naphthyl group substituted at any one or more of 2- to 8-positions thereof.

The term "aralkyl" and "arylalkyl" as used herein refers to alkyl groups as defined herein in which a hydrogen or carbon bond of an alkyl group is replaced with a bond to an aryl group as defined herein. Representative aralkyl groups include benzyl and phenylethyl groups and fused (cycloalkylaryl)alkyl groups such as 4-ethyl-indanyl. Aralkenyl groups are alkenyl groups as defined herein in which a hydrogen or carbon bond of an alkyl group is replaced with a bond to an aryl group as defined herein.

The term "arylenyl" as used herein refers to divalent groups that are derived by removing two hydrogen atoms from an "arylalkyl" group. Examples of arylenenyl groups include the group:

wherein the wavy lines represent the points of attachment.

The term "heterocyclyl" as used herein refers to substituted or unsubstituted aromatic and non- aromatic ring compounds containing 3 or more ring members, of which, one or more is a heteroatom such as, but not limited to, N, O, and S. Thus, a heterocyclyl can be a cycloheteroalkyl, or a heteroaryl, or if polycyclic, any combination thereof. Heterocyclyl groups can include 3 to about 20 ring members, whereas other such groups have 3 to about 15 ring members. Heterocyclyl groups include heterocyclyl groups that include 3 to 8 carbon atoms (C3-Cs), 3 to 6 carbon atoms (C3-Ce) or 6 to 8 carbon atoms (Ce-Cs). A heterocyclyl group designated as a C2-heterocyclyl can be a 5 -ring with two carbon atoms and three heteroatoms, a 6-ring with two carbon atoms and four heteroatoms and so forth. Likewise, a C/rheterocyclyl can be a 5-ring with one heteroatom, a 6-ring with two heteroatoms, and so forth. The number of carbon atoms plus the number of heteroatoms equals the total number of ring atoms. A heterocyclyl ring can also include one or more double bonds. A heteroaryl ring is an example of a heterocyclyl group. The phrase "heterocyclyl group" includes fused ring species including those that include fused aromatic and non-aromatic groups. Representative heterocyclyl groups include, but are not limited to piperidynyl, piperazinyl, morpholinyl, furanyl, pyrrolidinyl, pyridinyl, pyrazinyl, pyrimidinyl, triazinyl, thiophenyl, tetrahydrofuranyl, pyrrolyl, oxazolyl, imidazolyl, triazyolyl, tetrazolyl, benzoxazolinyl, and benzimidazolinyl groups.

The term "alkoxy" as used herein refers to an oxygen atom connected to an alkyl group, including a cycloalkyl group, as are defined herein. Examples of linear alkoxy groups include but are not limited to methoxy, ethoxy, propoxy, butoxy, pentyloxy, hexyloxy, and the like. Examples of branched alkoxy include but are not limited to isopropoxy, sec-butoxy, tert-butoxy, isopentyloxy, isohexyloxy, and the like. Examples of cyclic alkoxy include but are not limited to cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, and the like. An alkoxy group can include about 1 to about 12, about 1 to about 20, or about 1 to about 40 carbon atoms bonded to the oxygen atom, and can further include double or triple bonds, and can also include heteroatoms. For example, an allyloxy group or a methoxyethoxy group is also an alkoxy group within the meaning herein, as is a methylenedioxy group in a context where two adjacent atoms of a structure are substituted therewith.

The term "amine" as used herein refers to primary, secondary, and tertiary amines having, e.g., the formula N(group)3 wherein each group can independently be H or non-H, such as alkyl, aryl, and the like. Amines include but are not limited to R-NEb, for example, alkylamines, arylamines, alkylarylamines; R2NH wherein each R is independently selected, such as dialkylamines,

diarylamines, aralkylamines, heterocyclylamines and the like; and R3N wherein each R is

independently selected, such as trialkylamines, dialkylarylamines, alkyldiarylamines, triarylamines, and the like. The term "amine" also includes ammonium ions as used herein.

The terms "halo," "halogen," or "halide" group, as used herein, by themselves or as part of another substituent, mean, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom.

The term "haloalkyl" group, as used herein, includes mono-halo alkyl groups, poly-halo alkyl groups wherein all halo atoms can be the same or different, and per-halo alkyl groups, wherein all hydrogen atoms are replaced by halogen atoms, such as fluoro. Examples of haloalkyl include trifluoromethyl, 1, 1-dichloroethyl, 1,2-dichloroethyl, l,3-dibromo-3,3-difluoropropyl, perfluorobutyl, and the like.

As used herein, the term "hydrocarbyl" refers to a functional group derived from a straight chain, branched, or cyclic hydrocarbon, and can be alkyl, alkenyl, alkynyl, aryl, cycloalkyl, acyl, or any combination thereof. Hydrocarbyl groups can be shown as (C _a -Cb)hydrocarbyl, wherein a and b are integers and mean having any of a to b number of carbon atoms. For example, (Ci- C hydrocarbyl means the hydrocarbyl group can be methyl (Ci), ethyl (C2), propyl (C3), or butyl (C4), and (Co-Cb)hydrocarbyl means in certain embodiments there is no hydrocarbyl group.

As used herein, the term "salts" and "pharmaceutically acceptable salts" refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic groups such as amines; and alkali or organic salts of acidic groups such as carboxylic acids. Pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, and nitric; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2- acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, and isethionic, and the like.

Pharmaceutically acceptable salts can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. In some instances, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, the disclosure of which is hereby incorporated by reference.

The term "solvate" means a compound, or a salt thereof, that further includes a stoichiometric or non-stoichiometric amount of solvent bound by non-covalent intermolecular forces. Where the solvent is water, the solvate is a hydrate.

The term "prodrug" means a derivative of a compound that can hydrolyze, oxidize, or otherwise react under biological conditions (in vitro or in vivo) to provide an active compound, particularly a compound according to the instant disclosure. Examples of prodrugs include, but are not limited to, derivatives and metabolites of compounds described herein that include biohydrolyzable moieties such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, biohydrolyzable ureides, and biohydrolyzable phosphate analogues. Specific prodrugs of compounds with carboxyl functional groups are the lower alkyl esters of the carboxylic acid. The carboxylate esters are conveniently formed by esterifying any of the carboxylic acid moieties present on the molecule. Prodrugs can typically be prepared using well-known methods, such as those described by Burger's Medicinal Chemistry and Drug Discovery 6th ed. (Donald J. Abraham ed., 2001, Wiley) and Design and Application of Prodrugs (H. Bundgaard ed., 1985, Harwood Academic Publishers GmbH). EXAMPLES

The following examples are offered by way of illustration. But the present disclosure is not limited to the examples given herein.

Example 1

The Ligand Binding Landscape of Diacylglycerol Kinases

Introduction

Diacylglycerols (DAGs) and phosphatidic acid (PA) play roles in biology as basic components of membranes, intermediates in lipid metabolism, and secondary messengers in cellular signaling (Carrasco and Merida, 2007; Fang et al., 2001). Cells regulate intracellular DAG and PA levels through metabolic networks that utilize distinct enzymes to produce or consume these secondary messengers/metabolites (Brown et al., 2017; Carrasco and Merida, 2007; Hsu et al., 2012; Shulga et al., 2011). One such enzymatic pathway of signal transduction is adenosine triphosphate (ATP)-dependent phosphorylation of DAGs to biosynthesize phosphatidic acid (PA, Figure 1A) by a set of lipid kinases collectively known as diacylglycerol kinases (Shulga et al., 2011) (DGKs). DAG and PA are lipid messengers that alter localization (Takai et al, 1979), activation (Newton and Koshland, 1989), and protein-protein interactions (Fang et al., 2001) of distinct sets of receptor proteins. Consequently, disruption of the same DGK protein in different cell types can result in opposing effects that can be leveraged, for example, in cancer to simultaneously block tumor growth and activate antitumor immunity (Merida et al., 2017; Sakane et al., 2016). Since DAG and PA serve as intermediates in lipid metabolism, DGKs are uniquely positioned as regulators of the structural, bio-energetic, and signaling demands of cells.

Ten mammalian DGKs have been identified and classified into five subtypes based on structural features elucidated from primary sequence analysis (Figure IB). At the N-terminus, DGKs contain at least two cysteine-rich zinc finger-like motifs similar to CI domains found in protein kinase C (Carrasco and Merida, 2007) (PKC). DGKs contain a C-terminal catalytic domain composed of a conserved catalytic region (SMART domain (Schultz et al., 1998) DAGKc, SM000046), which is present in other eukaryotic lipid kinases and DGKs from Gram-positive bacteria (Adams et al., 2016), followed by an accessory subdomain (DAGKa, SM000045) of unknown function (Merida et al., 2017). While DGKs share the same basic domain organization, individual subtypes differ in regulatory domains proposed to mediate metal binding (EF hand motifs), oligomerization (SAM domain), membrane association (PH domain), subcellular localization (MARCKS domain), or protein-protein interactions (ankyrin repeats, PDZ domain) (Shulga et al., 2011). Given the chemical diversity of DAG and PA lipids (Yetukuri et al., 2008), understanding the cross-talk between regulatory and catalytic domains of DGKs will be allow for assigning metabolic and signaling functions to individual isoforms.

Attempts to define the function of individual DGK domains have resulted in inconclusive results. ATP-binding motifs corresponding to the glycine-rich loops found in protein kinases (GxGxxG consensus sequence (Hanks et al., 1988; Hemmer et al., 1997)) were identified in the first CI and catalytic domains of DGKs (Sakane et al., 1990; Schaap et al., 1994). Mutation of lysines in these motifs, which abolishes ATP binding and protein kinase activity, did not affect catalytic function of DGKs and led others to hypothesize the existence of a DGK-specific ATP binding motif that remains to be defined (Sakane et al., 1996; Schaap et al., 1994). The role of CI domains in DGK function is also enigmatic. With the exception of gamma and beta isoforms (Shindo et al., 2003), the CI domains of DGKs lack conserved residues identified as being required for DAG binding in other proteins including PKC (Hurley and Misra, 2000). In vitro biochemical studies measuring activity of CI truncation mutants have produced conflicting reports with regards to whether CI motifs are required (Abe et al., 2003; Houssa et al., 1997; Santos et al., 2002) or dispensable (Merino et al., 2007; Sakane et al., 1996) for maximal DGK catalytic activity.

Thus, DGK active sites remain ill-defined and, combined with the lack of crystal structures for mammalian DGKs, have limited the understanding of substrate and inhibitor binding. As a result, current DGK inhibitors consist of compounds with poor specificity within the DGK superfamily (de Chaffoy de Courcelles et al., 1989; de Chaffoy de Courcelles et al., 1985) or lack selectivity measurements against other lipid and protein kinases (Boroda et al., 2017; Liu et al., 2016; Purow, 2015). Thus, methods that provide information on small molecule binding mode and selectivity are needed to guide development of isoform-selective DGK inhibitors. Selective DGK inhibitors are needed to study isoforms where knockout mice viability is an issue (Crotty et al., 2006) and to help realize the translational potential of targeting specific forms, e.g. DGK-alpha (DGKa), for anticancer (Dominguez et al., 2013) and immunotherapy applications (Prinz et al., 2012).

Here, ATP acyl phosphate activity-based probes (Patricelli et al., 2011; Patricelli et al., 2007) and quantitative mass spectrometry were used to discover ATP- and inhibitor-binding sites of representative members of all five principal DGK subtypes. The findings define, for the first time, the ATP binding motif of DGKs that is distinct from protein kinases and identifies the DAGKa subdomain as a novel region mediating ATP binding. A fragment of the DGKa inhibitor ritanserin was discovered that shows conservation of binding mode and enhanced selectivity against protein kinases, supporting the concept that the atypical CI and accessory region of the catalytic domain (DAGKa) are ligand- binding sites for developing DGKa -selective inhibitors. The studies demonstrate the utility of chemical proteomics to map ligand binding sites for fragment-based discovery of lipid kinase inhibitors.

Materials and Methods

Reagents REAQEN7 RESOURCE SOURCE

Recorafainani DMA

Software AS¾tOitt†ras

Cell Culture

HEK293T cells were cultured in DMEM with 10% FBS (U.S. Source, Omega Scientific) and 1% L-glutamine (Thermo Fisher Scientific) in 10cm ² plates. SILAC HEK293T cells were cultured in DMEM for SILAC (Fisher Scientific) supplemented with 10% dialyzed FBS (Omega Scientific) and either 'Light' ¹² C, ¹⁴ N-labeled lysine and arginine or 'Heavy' ¹ C, ¹⁵ N-labeled lysine and arginine (lOOug/mL) in 10cm ² plates. Light or heavy amino acids were incorporated for at least 5 passages prior to utilizing SILAC HEK293T cells for experiments. All cells were grown to -80% confluency in a 37°C incubator with 5% CO ² .

Transient transfection.

Recombinant DGK proteins were produced by transient transfection of HEK293T cells with recombinant DNA. pDONR223-DGKK was a gift from William Hahn & David Root (Addgene plasmid # 23487). pCSF 107mT-GATEWAY-3 '-FLAG was a gift from Todd Stukenberg (Addgene plasmid # 67619). pCSF107mT-DGKK-FLAG construct was generated by recombination of the Addgene plasmids using the Gateway cloning system (Invitrogen). All other vectors were gifted to Dr. Kevin Lynch (University of Virginia, School of Medicine) by Dr. Kaoru Goto (Y amagata University, School of Medicine) and Dr. Fumio Sakane (Chiba University) and were kindly shared with us: pcDNA3 -FLAG-DGKA (rat), pCMV-Tag2B-FLAG-DGKQ (human), pcDNA3-DGKE- 3xFlag (human), and pCMV-SPORT6-HA-DGKZ (human). HEK293T cells were plated at a concentration of 400,000 cells in complete DMEM and grown to 50-60% confluency. A

polyethyleneimine (PEI) stock solution was prepared (lmg/mL, pH 7.4) and filter sterilized. Serum- free DMEM (600 μί) was mixed gently with 2.6 μg DNA and 20 of sterile PEI (1 mg/mL, pH 7.4) in a sterile microfuge tube. Mixtures were incubated for 30 min at 25 °C. The mixture was then added drop-wise to each 10 cm ² plate, rocked back and forth to mix, and placed back in the incubator. Cell pellets were harvested after two full days of growth, snap-frozen in liquid N2, and stored at -80°C until use. Recombinant proteins were produced by transient transfection in SILAC HEK293T cells using the procedure described above, except that cells were plated at a concentration of 1 x 10 ⁶ cells per 10 cm ² plate and grown to -70% confluency prior to introducing transfection mixture.

Western blot analysis of recombinant protein expression.

Cell lysates were separated via centrifugation at 100,000 x g for 45 min at 4 °C. Proteins separated by SDS-PAGE (7.5% polyacrylamide, TGX Stain-Free Mini Gel) at 150 V for 55 min. Gel transfers were performed using the Bio-Rad Trans-Blot Turbo RTA Midi Nitrocellulose Transfer Kit with a Bio-Rad Trans-Blot Turbo Transfer System (25V, 10 min). The nitrocellulose blot was then incubated in blocking solution (30 mL, 5% Milk in TBS-T ( 1.5 M NaCl, 0.25 M Tris pH 7.4 in ddH ₂ 0)) for 1 h at 25 °C with gentle shaking. The blot was then transferred immediately to primary antibody solution (1 : 1,000 anti-FLAG or 1 : 10,000 anti-HA in TBS-T) and incubated overnight at 4°C with gentle shaking. The blot was then rinsed 5 times for 5 min in TBS-T, transferred immediately into secondary antibody solution (1: 10,000 anti-species DyLight 550 or DyLight 650 in TBS-T), and incubated for 1 h at 25 °C with gentle shaking. The blot was then rinsed 5 times for 5 min in TBS-T, transferred into ddFbO, and imaged by in-blot fluorescence scanning on a ChemiDoc MP Imaging System.

Preparation of cell lysates for gel-based chemical proteomics.

Cell pellets were resuspended in kinase buffer (Dulbecco's PBS (DPBS, Hyclone), 20 mM MgC , EDTA-free protease inhibitors (Pierce)) and then lysed by sonication (3 x 1 sec pulse, 20% amplitude). The cell lysates were then subjected to centrifugation (100,000 x g, 45 min at 4 °C) to isolate the cytosolic fraction in the supernatant and the membrane fraction as a pellet. The membrane pellet was resuspended in kinase buffer by sonication. For all further analyses, only the soluble (cytosolic) fraction was used to prevent the need for detergents, which have been shown to interfere with DGK activity (Y ada et al., 1990). The only exception was experiments involving DGKE;

recombinant DGKE protein was most prominently expressed in the membrane fraction and so this fraction was utilized to study DGKE enzyme (see Figure 8). Protein concentrations were measured using the Bio-Rad DC protein assay. Samples were stored at -80 °C until use.

Gel-based chemical proteomic assay.

Proteome concentration was adjusted to 2 mg/mL in kinase buffer. Proteomes were first pre- treated with compound (0.6 μί, 50X stock in DMSO) mixed with gentle flicking, and incubated for 30 min at 25 °C in a microfuge tube (30 reaction volume). Desthiobiotin ATP acyl phosphate nucleotide probe (0.5 mM in ddH ² 0) was then added to each sample (0.6 μί, 10 μΜ final) and incubated for 30 min at 25 °C. Reactions were then quenched with 10 μί _^ of 4X SDS-PAGE loading buffer. Protein samples (15 μί) were loaded onto 4-20% TGX Stain-Free Protein Midi Gel and resolved by SDS-PAGE at 150V for 55 min. Proteins were then transferred to a nitrocellulose blot by Bio-Rad Trans-Blot Turbo Transfer System (25V, 10 min) to enhance sensitivity. The nitrocellulose blot was then incubated in blocking solution (30 mL, 3% BSA in TBS-T) for 1 h at 25 °C with gentle shaking. The blot was then transferred immediately to antibody solution (30 mL, 5% BSA in ddH ₂ 0 with 0.1% Tween20 and 1:3000 Streptavidin DyLight 550) and incubated for 2 h at 25 °C with gentle shaking. The blot was then rinsed 5 times for 5 min in TBS-T, and then transferred into ddH ₂ 0. The blot was then imaged by in-blot fluorescence scanning on a ChemiDoc MP Imaging System.

Fluorescence intensity signals were normalized to total lane protein using the Bio-rad Stain Free imaging (Posch et al., 2013).

Preparation of cell lysates for ADP-glo assay.

The ADP-Glo DAG phosphorylation substrate assay was adapted from Sato et al (Sato et al., 2013). Transfected HEK cells expressing recombinant FLAG-DGKA were harvested in DPBS and centrifuged at 1400 x g for 3 min. Supernatant was removed and 1 mL Lysis Buffer (50 mM HEPES (pH 7.2), 150 mM NaCl, 5 mM MgCl ₂ , 1 mM DTT, 1 mM phenylmethysulfonyl chloride,

Phosphatase Inhibitor Cocktail 2 (Sigma-Aldrich), and EDTA-Free Protease Inhibitor Mini Tablets (Pierce)) was added and cells re-suspended. Solutions were sonicated (3 x 1 sec pulse, 20% amplitude) and then centrifuged at 400 x g for 5 min. Supernatant was separated and protein concentrations were measured using the Bio-Rad DC protein assay and diluted in Lysis Buffer as appropriate. Samples were stored at -80°C until use.

ADP-glo DAG phosphorylation substrate assay.

Micelles were prepared from lipid stocks as follows: Reaction Buffer (50 mM MOPS (pH

7.4), 1 mM DTT, 100 mM NaCl, 20 mM NaF, and 1 μΜ CaCl ₂ ) was prepared in ddH ₂ 0. From this stock, a solution of Reaction Buffer with 50 mM MgCl ₂ and 1 mM ATP ('Reaction Initiator') and a solution of 0.3% Triton-XlOO in Reaction Buffer ('Triton Buffer') were separately prepared. 1, 2- dioleoyl-sn-glycerol (DG) and l,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) in chloroform were mixed and then dried under nitrogen. Triton Buffer was added to the dried lipids to a final concentration of 10 mM DG and 8 mM DOPS. This solution was incubated at room temperature for 5 min with gentle shaking, followed by sonication (3 x 1 sec pulse, 20% amplitude). The micelles were then diluted 4-fold in reaction buffer to yield the final micelle buffer. 1 mg of lysate was aliquoted into each well of a 96 well plate, followed by micelle buffer to a final volume of 20 μί. \9 μί _^ οΐ this mix was added to 1 of DMSO or inhibitor solution and incubated at 30 °C for 30 min. After incubation, 5 of reaction initiator was added to each well and mixed thoroughly, followed by aliquoting 5 μί of each reaction mixture to a 96-well half area black polystyrene plate and incubated at 30 °C for 30 min. At this point the procedure for the ADP-GloTM assay (Promega) was performed. 5 μί of 'ADP-Glo Reagent' was added to each well, mixed thoroughly, and allowed to incubate at 25 °C for 40 min. Then 10 μί of the 'Kinase Detection Reagent' was added to each well, mixed thoroughly, and allowed to incubate at 25 °C for 40 min. Luminescence was measured with no filter and an integration time of 1 sec per well on a BMG Labtech CLARIOstar plate reader.

Sample preparation for quantitative LC-MS analysis using ATP acyl phosphates.

Proteomes were diluted to 2 mg/mL in kinase buffer. The light and heavy proteomes (0.5 mg, 250 μί total reaction volume) were pre-treated with vehicle or compound, respectively (5 μί, DMSO (light) or 50X stock in DMSO (heavy)), mixed gently, and incubated at 25 °C for 30 min.

Desthiobiotin ATP acyl phosphate nucleotide probe (0.5 mM in ddH ₂ 0) was then added to each sample (5 μί, 10 μΜ final), mixed gently, and allowed to incubate at 25 °C for 30 min. After incubation, matched light and heavy proteomes were transferred and mixed in a 1 : 1 ratio in a two- dram vial containing 4: 1:3 MeOH/CHCl ₃ /H ₂ 0 (2 mL MeOH, 500 μΐ, CHC1 ₃ , 1.5 mL H ₂ 0) for extraction of proteins to remove excess probe, quickly vortexed, and centrifuged at 1,400 x g for 3 min to pellet protein. Organic and aqueous layers were removed using a Pasteur pipette, and the protein pellet was transferred to a screw-top tube in 600 μί MeOH. A second extraction was performed by adding CHCh (150 μί) and H ₂ 0 (600 μί) to each sample, vortexed, and centrifuged at 1,400 x g for 3 min to pellet protein. Organic and aqueous layers were removed by pipetting, MeOH added to pellet (600 μί) and pellets were re-suspended by sonication (3 x 1 sec pulse, 20% amplitude) for a final extraction. Samples were then centrifuged at 17,000 x g for 5 min to pellet protein and MeOH was removed by pipetting. The pellets were re-suspended in 10 M urea/25 mM ammonium bicarbonate (500 mL), brought to a final volume of 1 mL with 25 mM ammonium bicarbonate, reduced with 10 mM DTT for 15 min at 65 °C, allowed to cool, and then alkylated with 40 mM iodoacetamide for 30 min at 25°C in the dark. To desalt the samples, each was transferred to a two- dram glass vial, and to the vial 4: 1:2 MeOH/CHCl ₃ /H ₂ 0 (2 mL MeOH, 500 CHC1 ₃ , 1 mL H ₂ 0) was added. The vials were vortexed quickly, spun at 1,400 x g for 3 min to pellet protein, and aqueous and organic layers were removed using a Pasteur pipette. The resulting protein pellet was transferred to a screw-top tube in 600 MeOH, and then CHCI ₃ (150 μί) and H ₂ O (600 μί) were added to extract protein a second time. The samples were vortexed quickly, centrifuged at 1,400 x g to pellet protein, and the aqueous and organic layers were removed by pipetting. Resulting protein pellet was suspended in MeOH (600 μί) via sonication (3 x lsec pulse, 20% amplitude), centrifuged at 17,000 x g for 5 min to pellet protein, and MeOH removed by pipetting. Protein pellets were then re-suspended in 25 mM ammonium bicarbonate (500 μί) and digested with 7.5 μg Trypsin Lys-C (Promega, 15 μί, 0.5 μg/μL) for 3 h at 37 °C. Avidin-agarose beads (Thermo Scientific Pierce, 100 μί aliquot per sample) were washed three times by adding 10 mL DPBS, centrifuged at 1,400 x g for 1 min, and decanting. This wash step was repeated for a total of 3 times. Digested protein samples were mixed with washed avidin beads (100 μί) and brought to a volume of 5.5 mL with DPBS in a 15 mL conical and rotated for 1 h to enrich samples for the covalent desthiobiotin modification. The beads were washed with 25 mM ammonium bicarbonate (3X with 10 mL, centrifuge at 1,400 x g for 3 min, decant) and then ¾0 (3X with 10 mL, centrifuge at 1,400 x g for 3 min, decant). Washed beads were then transferred to a low -bind microfuge tube, centrifuged at 1,400 x g for 3 min, allowed to rest for 1 min to settle beads, and then excess ¾0 was removed carefully using a gel-loading pipette tip. To elute peptides, 100 μΐ _^ of elution buffer (50% acetonitrile, ACN; 0.1% formic acid) was added to each sample and incubated for 3 min. Beads were spun down at 1,400 x g for 3 min, allowed to rest for 1 min to settle beads, and then 75 μΐ _^ of peptide-containing supernatant was removed carefully using a gel-loading pipette tip and transferred to a new low bind centrifuge tube. This step was repeated two more times with 75 μΐ _^ of elution buffer and all eluent were collected into the same centrifuge tube (-225 μί _^ total). Peptides were dried on a speed vacuum, resulting peptide samples acidified in 5% (v/v) formic acid, and stored at -80 °C until analysis.

LC-MS/MS analysis of SILAC samples.

The peptide samples were analyzed by liquid chromatography-mass spectrometry. An integrated autosampler-LC (Ultimate 3000 RSLC nanoSystem, Dionex) was used to load the peptides onto a trap column (Nano-Trap, Thermo Scientific, 2 cm, 5 μπι C 18) and washed for 2 minutes with 1% B (80% ACN, 1% formic acid). The peptides were eluted from the trap column and through a homemade nanocapillary analytical column (20 cm, 5 μπι C18 packed in 360 μπι o.d. x 75 μπι i.d. fused silica), with an integrated electrospray tip, using a 180 min 1-95% reverse-phase LC gradient (A: 0.1% formic acid; B: 80% ACN, 0.1% formic acid) with the following parameters: 0-2 min 1% B, 400 nL/min; 2-144 min to 95% B, 300 nL/min; 144.1-180 min 1% B, 400 nL/min. The eluting peptides were electrosprayed into an Orbitrap Q Exactive Plus mass spectrometer (Thermo Scientific), which was operated with a top 10 data-dependent acquisition method that consisted of one full MS 1 scan (375 - 1,500 m/z) followed by 10 MS2 scans of the most abundant ions recorded in the MSI scan. For recombinant DGKE samples, a data-independent parallel reaction monitoring (PRM) method was used to detect DGKE peptides. One full MS I scan (375 - 1,500 m/z) was followed by MS2 scans of targeted parent ions from a curated inclusion list (DGKE: EKAPSLFSSR, +2 charge state, 659.3617 m/z (light), 668.3729 m/z (heavy), 103.00-110.00 min). Data analysis was accomplished using the IP2 (Integrated Proteomics Applications) software package, in which

RawConverter was used to generate searchable MSI and MS2 data from the .raw file followed by using the ProLuCID algorithm to search the data against a modified human protein database (UniProt human protein database with rat DGKs, angiotensin I and vasoactive intestinal peptide standards; 40,660 proteins) with the following parameters: static carbamidomethyl modification of cysteine

(+57.0142 Da), differential modifications of oxidized methionine (+15.9949 Da) and desthiobiotin- labeled lysine residues (+196.1212 Da), added masses of the SILAC "heavy"-labeled amino acids (+10.0083 Da for R, +8.0142 Da for K), and trypsin enzyme specificity with 2 missed cleavages. The resulting MS2 spectra matches were assembled into protein identifications and filtered using

DTASelect 2.0 using the—mass,—modstat, and—trypstat options with a 1% peptide FDR. mzldent files corresponding to searches were generated in IP2-Integrated Proteomics Pipeline, mzXML spectra data was extracted from the raw file using RawConverter, and uploaded into Skyline -daily (Schilling et al., 2012) to determine SILAC ratios (SR) of light/heavy (vehicle/compound treated) peptides. Peptides used for analysis were assessed for quality in Skyline by the following criteria: isotope dot-product (iDOTP) > 0.8, ratio dot-product (rDOTP) > 0.8, and singletons defined by L/H ratios > 20 were set to 20. Dot-product values are measures of similarity between the precursor peak area and expected isotope distribution (iDOTP) and between the light and heavy peak area (rDOTP) as calculated in Skyline and described by Schilling et al (Schilling et al., 2012). Probe-modified peptides that met these criteria were manually inspected and integrated. Peptide ratios reported were normalized to DMSO/DMSO peptide ratios to account for potential variations in mixing and sample preparations. Additionally, reported DGK and FER peptides were verified by manual inspection of the raw data (MS I and MS2).

Sequence alignments and generation of sequence logos.

Lipid kinase sequences were obtained from Uniprot (http://www.uniprot.org/) and aligned using Clustal Omega (Goujon et al., 2010; Sievers et al., 2011). Sequence logos shown in Figure 5 were generated with WebLogo (Crooks et al., 2004; Schneider and Stephens, 1990)

(weblogo .threeplusone .com) .

DgkB monomer molecular model and alignment.

PDB model 2QV7 visualized and colored using PyMol software. Partial Structure -Aided Sequence Alignment completed as described previously (Miller et al, 2008) and added to Figure 11 using GIMP software package.

Statistical analysis and determination of IC50 values.

The percentage of enzyme activity remaining was determined by comparing integrated band intensities or luminescence of inhibitor- with DMSO-treated samples for gel-based chemical proteomic or ADP-glo assays, respectively. For both chemical proteomic and ADP-glo methods, nonlinear regression analysis was used to determine the IC ₅₀ values from a dose-response curve generated using GraphPad Prism. Data are shown as mean ± s.e.m. Determination of significance was performed by one-way ANOVA. All statistical analyses were performed using GraphPad Prism. Results

ATP acyl phosphates function as activity-based probes of DGKa.

To test whether ATP acyl phosphates (Figure 2A) can be used to profile DGK activity, the strategy was to transiently express DGKs and test recombinant enzymes directly in cell proteomes without the need for protein purification. It was reasoned that this approach would mitigate challenges with detection due to differences in endogenous DGK levels while permitting analyses on a proteomic scale. The initial studies focused on the alpha isoform (DGKa, Figure IB) given the availability of inhibitors and matching negative control compounds (Boroda et al., 2017) for the proof-of-principle experiments (Figure 2B). Overexpression of recombinant FLAG-tagged DGKa was confirmed by western blot (Figure 8) and used published DAG phosphorylation substrate assays (Sato et al., 2013) to measure recombinant DGKa activity (Figure 9A). Significantly higher DAG phosphorylation activity (~6-fold on average) was observed in DGKa- compared with mock-transfected or heat- denatured proteomes (Figure 9B). Furthermore, recombinant DGKa activity was blocked in a concentration-dependent manner using the DGKa inhibitor ritanserin (Boroda et al., 2017) compared with dimethyl sulfoxide (DMSO) vehicle-treated controls (IC ₅₀ = 25 μΜ, Figure 3A). Since ritanserin exhibits 5-HT2 receptor (5-HT2R) inhibitory activity (Barone et al., 1986), another 5-HT2R antagonist ketanserin was included (Boroda et al., 2017) (Figure 2B) to control for non-specific effects in the substrate assay. Ketanserin showed negligible activity against DGKa in the substrate assay, confirming the use of ritanserin and ketanserin as paired probes (i.e. DGK active and inactive inhibitors, respectively, at 100 μΜ; Figure 9B) suitable for testing in the chemical proteomics assay.

Next, it was determined whether one could use desthiobiotin-tagged, ATP acyl-phosphates (Patricelli et al., 2011; Patricelli et al., 2007) as a surrogate chemical proteomic assay for measuring recombinant DGKa activity in cell proteomes (Figure 2A). ATP acyl-phosphate probes enable global profiling of kinase activities by covalent attachment of reporter tags to conserved lysine residues in the ATP binding site of a wide range of kinases as well as other ATP -binding proteins (Patricelli et al., 2011; Patricelli et al., 2007). Initially, gel-based profiling experiments were preformed to allow rapid optimization of probe labeling parameters (Figure 10A). In brief, DGKot-HEK293T soluble lysates were reacted with the ATP acyl-phosphate probe, desthiobiotin-modified proteins separated by SDS-PAGE, transferred to a nitrocellulose membrane, and probe-modified proteins detected using a fluorescently-labeled streptavidin. Concentration dependent labeling of a -80 kDa fluorescent band in DGKa- but not mock-transfected HEK293T proteomes was observed (Figure 10B). It was confirmed by western blot that differences in fluorescence signals in the probe binding assay were not due to expression levels of recombinant DGKa (Bottom panel, Figure 10B).

From these studies, experimental conditions were identified where ATP acyl-phosphate labeling of DGKa was not saturating to allow competitive profiling of reversible inhibitors

(Adibekian et al, 2012) (10 μΜ ATP probe, 30 min; Figure IOC). Using these kinetically-controlled conditions, it was shown that pretreatment with ritanserin but not ketanserin resulted in concentration- dependent blockade of probe labeling (IC ₅₀ = 57 μΜ, Figure 3B and Figure S 10D). The non-selective DGK inhibitors, R59949 (de Chaffoy de Courcelles et al., 1989) and R59022 (de Chaffoy de

Courcelles et al., 1985), were analyzed to show that the gel activity assay can be used to generally profile inhibitor activity against DGKa (Figure 10E). Finally, it was shown that treatment with free ATP (1 mM) resulted in global reductions in fluorescent protein signals (Figure 3C). These results support specific detection of probe labeling events occurring in the ATP binding site of recombinant DGKa as well as other native proteins detected in HEK293T cell proteomes. In all of the probe- labeling studies, changes in fluorescent signals in compound-treated samples were not due to differences in DGKa protein levels as confirmed by western blot analysis (Bottom panels; Figure 3C, Figure 10D and E). Collectively, the comparable potency values determined using substrate- (Figure 3A) versus chemical proteomic-assays (Figure 3B) demonstrate that ATP acyl phosphates are capable of measuring authentic DGKa activity with the advantage of enabling rapid assessment of compound activity across ATP -binding sites detected in native cell proteomes (Figure 3C).

Mapping the ATP binding site of DGKa using quantitative chemical proteomics.

Results from gel profiling analyses demonstrated the probe binding of DGKa is competed by

ATP substrate. While suited for rapid screening, gel-based chemical proteomic assays do not provide information on site of binding of compounds. Thus, a liquid chromatography-mass spectrometry (LC- MS) assay was implemented to discover the ATP binding site(s) of DGKa. For these studies, DGKa was overexpressed in isotopically light and heavy amino acid-labeled HEK293T cells to enable quantitative LC-MS by stable isotope labeling with amino acids in cell culture (SILAC (Mann, 2006), Figure 4A). In brief, light and heavy DGKot-HEK293T lysates were treated differentially with DMSO vehicle or free ATP ( 1 mM) respectively, prior to addition of ATP acyl phosphate to label active site lysines. After probe labeling, light and heavy proteomes were combined, digested with trypsin protease, and desthiobiotin-modified peptides were enriched by avidin affinity chromatography and analyzed by LC-MS/MS to identify and quantify isotopically tagged active-site peptides from DGKa (Figure 4A, see Materials and Methods for more details).

Using the quantitative chemical proteomics assay, two probe-labeled peptides were identified that were highly competed with ATP treatment as determined by SILAC ratios (SR) of MSI chromatographic peak areas >5 in DMSO/ATP comparisons (Figure 4B and Table 1 and 1A. All peptides reported met quality control criteria and were observed in 2 biological replicates (see

Materials and Methods for more details). The sites of labeling for probe-modified peptides of DGKa were confirmed by identifying ions corresponding to peptide fragments that contain the modified lysine residue in MS2 spectra (red asterisk, Figure 4B). Both ATP -sensitive peptides are located within the predicted catalytic domain, albeit at different subdomain regions (K377 - DAGKc, SR = 16.3; K539 - DAGKa, SR = 16.4; Figure 4B). Comparison of these peptide sequences with ATP- binding motifs found in protein kinases (Hanks et al., 1988; Sakane et al., 1990) revealed no apparent homology, supporting previous speculation that DGKs mediate ATP binding through a non-canonical binding motif (Schaap et al., 1994). Closer inspection of the DAGKc peptide did reveal homology with ATP binding sites of DgkB from S. aureus, and placement of K377 at the homologous residue in the bacterial DGK crystal structure (threonine 12) positions this lysine in vicinity of phosphate groups of ADP (Miller et al., 2008) (Figure 11). The second ATP-sensitive peptide (K539, Figure 4B) is located in the poorly annotated DAGKa subdomain that has not been implicated in ATP binding in DGKa or any other DGK isoform. These results help explain previous findings from other groups showing that C-terminal truncations (which remove the DAGKa subdomain) result in impaired DGK catalytic activity (Los et al., 2004).

Table 1 (SEQIDNOs: 17-68)

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

EANPEKFNS Diacylglycerol kinase zeta

DGKZ DAGKa Q13574 16.7 1.4 1.8 1.1

R [Homo sapiens (Human)]

Diacylglycerol kinase

KTCGSSDVL

DGKQ CI P52824 theta [Homo sapiens 3.6 0.9 1.3 0.7

AGVR

(Human)]

LPPDSCPLLV Diacylglycerol kinase

DGKQ FVNPKSGGL DAGKc P52824 theta [Homo sapiens 7.6 1.2 1.1 0.9

K (Human)]

Diacylglycerol kinase

DGKQ EEEPGKFTSR DAGKa P52824 theta [Homo sapiens 14.4 1.1 1.4 1.2

(Human)]

Native kinases

in HEK293T

5 '-AMP -activated protein

AAPK1/AAPK DLKPENVLL kinase catalytic subunit

Lys2 Q13131 9.1 1.4 2.4 1.1 2 DAHMNAK alpha- 1 [Homo sapiens

(Human)]

B-Raf proto-oncogene

DLKSN IFLH serine/threonine-protein

BRAF Lys2 P15056 >20 1.6 1.8 1.1

EDLTVK kinase [Homo sapiens

(Human)]

Cell division control

DLKPQNLLID

CDK1 Lys2 P06493 protein 2 homolog [Homo 8.4 1.4 2.4 1.1

DKGTIK

sapiens (Human)]

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

Cell division protein

DLKPQNLLIN

CDK2 Lys2 P24941 kinase 2 [Homo sapiens >20 1.6 2.9 0.7

TEGAIK

(Human)]

Cell division protein

DLKPQNLLIN

CDK5 Lys2 Q00535 kinase 5 [Homo sapiens 10.7 1.3 1.9 1.1

R

(Human)]

Serine/threonine-protein

CHK2 VAIKIISK Lysl 096017 kinase Chk2 [Homo >20 1.6 2.2 0.2 sapiens (Human)]

VSDFGLTKE Tyrosine-protein kinase

CSK ASSTQDTGK ACT P41240 CSK [Homo sapiens 15.8 1.2 1.8 1.1

LPVK (Human)]

Interferon-induced,

DLKPSNIFLV double-stranded RNA-

E2AK2 Lys2 P19525 >20 1.3 2.8 1.2

DTK activated protein kinase

[Homo sapiens (Human)]

Proto-oncogene tyrosine-

TSVAVKTCK protein kinase FER n=2

FER Lysl P16591 19.3 1.4 7.9 1.2

EDLPQELK Tax=Homo sapiens

RepID=FER HUMAN

AIQFLHQDSP Interleukin-1 receptor-

IRAKI SLIHGDIKSS Lys2 P51617 associated kinase 1 [Homo 14.7 1.4 2.6 2.2

NVLLDER sapiens (Human)]

KCC1D LFAVKCIPK Lysl Q8IU85 Calcium/calmodulin- >20 1.5 2.3 1.1 dependent protein kinase

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

type ID [Homo sapiens

(Human)]

Calcium/calmodulin- dependent protein kinase

IPTGQEYAA

KCC2D Lysl Q13557 type II delta chain n=2 10.3 1.5 2.3 1.2

KIINTK

Tax=Euarchontoglires

RepID=KCC2D HUMAN

Calcium/calmodulin-

TSTQEYAAKI dependent protein kinase

KCC2G Lysl Q13555 14.7 1.5 2.7 1.6

INTK type II gamma chain

[Homo sapiens (Human)]

Ribosomal protein S6

LTDFGLSKE

KS6A1 ACT Q15418 kinase alpha 1 [Homo 19.5 1.4 2.1 1.3

AIDHEK

sapiens (Human)]

Ribosomal protein S6

KS6A1/KS6A2 DLKPENILLD

Lys2 Q15418 kinase alpha 1 [Homo 19.4 1.4 2.0 1.2 /KS6A3 EEGHIK

sapiens (Human)]

Ribosomal protein S6

VLGTGAYGK

KS6A4/KS6A5 ATP Loop 075676 kinase alpha 4 [Homo >20 1.3 2.2 1.1

VFLVR

sapiens (Human)]

Ribosomal protein S6

DLKPENIML kinase 1 (EC 2.7.1.37)

KS6B1 Lys2 P23443 1.3 1.0

NHQGHVK (S6K) (S6K1) (70 kDa >20 1.2

ribosomal protein S6

kinase 1) (p70 S6 kinase

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

alpha) (p70(S6K)-alpha)

[Homo sapiens (Human)]

Ribosomal protein S6

DLKPENIMLS

KS6B2 Lys2 Q9UBS0 kinase 2 [Homo sapiens 19.2 1.1 1.4 1.7

SQGHIK

(Human)]

Serine/threonine-protein

LATS1 ALYATKTLR Lysl 095835 kinase LATS 1 [Homo >20 1.2 1.8 1.4

sapiens (Human)]

Mitogen-activated protein

kinase kinase kinase 2 n=3

M3K2/M3K3 DIKGANILR Lys2 Q9Y2U5 19.2 1.1 1.2 1.0

Tax=Homo sapiens

RepID=M3 K2 HUMAN

Mitogen-activated protein

DIKGANIFLT

M3K4 Lys2 Q9Y6R4 kinase kinase kinase 4 6.8 1.2 1.9 0.8

SSGLIK

[Homo sapiens (Human)]

Mitogen-activated protein

DIKGANILLT kinase kinase kinase

M4K3 Lys2 Q8IVH8 14.2 1.4 1.8 1.1

DNGHVK kinase 3 [Homo sapiens

(Human)]

Mitogen-activated protein

M4K4/MINK1/ DIKGQNVLL kinase kinase kinase

Lys2 095819 >20 1.3 1.8 1.1 TNIK TENAEVK kinase 4 [Homo sapiens

(Human)]

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

Mitogen-activated protein

NVHTGELAA kinase kinase kinase

M4K5 Lysl Q9Y4K4 >20 1.3 2.4 0.9

VKIIK kinase 5 [Homo sapiens

(Human)]

Mitogen-activated protein

DIKGANILLT kinase kinase kinase

M4K5 Lys2 Q9Y4K4 >20 1.3 1.9 1.3

DHGDVK kinase 5 [Homo sapiens

(Human)]

MAP/microtubule affinity-

MARK3/MAR

EVAVKIIDK Lysl P27448 regulating kinase 3 [Homo >20 1.4 2.0 1.1 K4

sapiens (Human)]

Dual specificity mitogen-

MP2K1/MP2K DVKPSNILV activated protein kinase

Lys2 Q02750 >20 1.3 1.9 0.9 2 NSR kinase 1 n=4 Tax=Eutheria

RepID=MP2Kl HUMAN

Dual specificity mitogen-

DVKPSNVLI activated protein kinase

MP2K3 Lys2 P46734 19.1 1.4 1.7 1.2

NK kinase 3 [Homo sapiens

(Human)]

Dual specificity mitogen-

DIKPSNILLD activated protein kinase

MP2K4 Lys2 P45985 >20 1.3 1.6 0.9

R kinase 4 [Homo sapiens

(Human)]

HVPSGQIMA

MP2K6 Lysl P52564

VKR Dual specificity mitogen- >20 1.4 2.2 1.1 activated protein kinase

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

kinase 6 [Homo sapiens

(Human)]

Serine/threonine-protein

SKNIFLTQNG

NEK3 ACT P51956 kinase Nek3 [Homo >20 1.0 2.2 1.0

K

sapiens (Human)]

PAB -dependent poly (A) -

VMDPTKILIT specific ribonuclease

PAN3 ATP Q58A45 >20 1.3 1.8 1.3

GK subunit [Homo sapiens

(Human)]

Phosphatidylinositol-5- phosphate 4-kinase type-2

FKEYCPQVF

PI42C C2 Q8TBX8 gamma n=l Tax=Homo 6.9 1.2 1.7 0.8

R

sapiens

RepID=PI42C_HUMAN

CFEISDADTK Serine/threonine-protein

PLK1 EVFAGKIVP Lysl P53350 kinase PLK1 [Homo 12.2 1.0 1.5 0.9

K sapiens (Human)]

RAF proto-oncogene

DMKSNNIFL serine/threonine-protein

RAF 1 Lys2 P04049 >20 1.4 3.9 2.1

HEGLTVK kinase [Homo sapiens

(Human)]

CTCL tumor antigen se20-

DLKAGNILFT

SLK Lys2 Q9H2G2 9 [Homo sapiens >20 1.3 3.0 1.5

LDGDIK

(Human)]

Ratios

Labeling Uniprot

Kinase name Peptide Annotation ATP Ketanserin Ritanserin RF001 site Accession

Serine/threonine-protein

DTVTIHSVG

kinase SMG1 n=4

SMG1 GTITILPTKT ATP Q96Q15 15.9 1.3 1.7 1.0

Tax=Homo sapiens

KPK

RepID=SMGl_HUMAN

Serine/threonine-protein

DLKAGNVL

STK10 Lys2 094804 kinase 10 [Homo sapiens 7.4 1.3 1.7 1.1

MTLEGDIR

(Human)]

Serine/threonine-protein

DIKAGNILLN

STK3/STK4 Lys2 Q13188 kinase 3 [Homo sapiens >20 1.2 1.6 0.9

TEGHAK

(Human)]

Serine/threonine-protein

DTGHVYAM

STK38 Lysl Q15208 kinase 38 [Homo sapiens 5.2 1.3 2.0 1.4

KILR

(Human)]

EVVAIKCVA Unc-51-like kinase 3

ULK3 Lysl Q6PHR2 >20 2.3 1.8 1.4

K [Homo sapiens (Human)]

Table 1A (SEQ ID NOs: 69-78)

DAGKc subdomain

Finally, a probe-modified peptide located in the first CI domain of DGKa was identified (K237, Figure 4B). The CI site was competed with ATP treatments (K237, SR = 2.4, -58% inhibition; Figure 4B and Table 1 and Table 1A but with lower potency compared with probe - modified peptides from DAGKc and DAGKa subdomains (-94% competition with ATP). The difference in sensitivity to ATP competition at CI versus DAGKc/DAGKa suggests that the latter sites largely mediate ATP binding of DGKa. The partial sensitivity of CI to ATP competition suggests the existence of a distinct binding site in the CI domain that can bind ATP probe separate from interactions at the DAGKc/DAGKa sites (Figure 4C). In summary, the LC-MS findings provide evidence that ATP acyl phosphate probes can map important binding regions of DGKa domains to reveal ATP (DAGKc/DAGKa) and other ligand binding sites (CI) important for mediating catalytic functions.

Chemical proteomic profiling of the DGK superfamily using ATP acyl phosphates.

Next, it was sought to expand the chemical proteomics analysis to other DGK subtypes to identify conserved and distinguishing features of active sites in comparison with type 1 DGKa. For these studies, a representative member from each of the DGK subtypes was chosen to test: kappa (DGKK (Imai et al., 2005)), type 2; epsilon (DGKs (Tang et al., 1996)), type 3; zeta (ϋϋΚζ (Goto and Kondo, 1996)), type 4; and theta (DGK6 (Houssa et al., 1997)), type 5 (Figure IB). Recombinant DGKs were transiently transfected in light and heavy HEK293T cells, protein overexpression confirmed by western blot (Figure 8), and recombinant lysates subjected to quantitative chemical proteomics (Figure 4A). The identified probe-modified peptides for each DGK isoform and their corresponding sensitivities to ATP competition are listed in Table 1 and 1A

Akin to DGKot, probe-modified peptides in CI, DAGKc, and DAGKa binding sites of ΟϋΚζ and DGK6 were identified (Figure 5A). Treatment with free ATP resulted in potent competition at DAGKc (K596, SR = 7.6) and DAGKa (K768, SR = 14.4) sites within the catalytic domain of DGK6 (Figure 5A and Table 1 and 1A. Similar inhibition profiles were observed for ΟϋΚζ with the exception of a lower sensitivity to ATP competition at the DAGKc (K500, SR = 2.9) compared with DAGKa site (K662, SR = 16.7, Figure 5A and Table 1 and 1A. Probe-modified peptides

corresponding to CI domains of both ΟϋΚζ (K323) and DGK6 (K202) showed moderate competition with ATP (SR ~3 for both isoforms, Figure 5A and Table 1 and 1A. Of the remaining subtypes, a single probe-modified peptide in the DAGKa subdomain of DGKK and DGKs were identified that were competed with ATP with high (K892, SR = 15.0) or moderate inhibition (K392, SR = 2.6; Figure 5A and Table 1 and 1A, respectively. Based on ATP sensitivity, the findings position the primary ATP binding site within the DAGKa subdomain of type 2 (DGKK), 3 (DGKs), and 4 (ΟϋΚζ) enzymes. Similar to DGKot, type 5 DGK6 likely requires both DAGKa and DAGKc regions for ATP substrate binding.

Multiple sequence alignments and sequence logo analysis (Crooks et al., 2004; Schneider and Stephens, 1990) were performed to identify a potential DGK-specific ATP binding motif. ATP- competed peptide sequences identified in the LC-MS analyses (Table 1 and 1A were used to discover potential regions of sequence conservation across all 5 DGK subtypes tested. The analyses identified clusters of amino acid conservation in regions that contained probe-modified lysines within both DAGKc (positions 7-17, Figure 5B) and DAGKa subdomains (positions 7-19, Figure 5C). The results were used to determine whether DGKs are probe-labeled at conserved lysines in the active site, which would provide preliminary evidence of a common ATP binding orientation. Closer inspection of the data revealed that the lysine showing highest conservation in the DAGKc motif was also probe modified with the highest frequency (position 9, Figure 5B). In contrast, the correlation between conserved lysines and frequency of probe modifications at these sites was less clear in the DAGKa motif. For example, probe modification of the lysine with highest conservation (position 19) was only observed in the DGKK active site peptide (Figure 5C). The identification of probe modifications at both conserved (DAGKc) and non-conserved lysines (DAGKa) in the DGK ATP binding site is different from protein kinases, which are probe modified largely at conserved lysines in the ATP binding site (Patricelli et al., 2007).

Inhibitor profiling to determine ritanserin binding mode and selectivity. Next it was asked whether one could use quantitative chemical proteomics to determine the binding mode and selectivity of inhibitors against DGK isoforms. Ritanserin was originally tested in the clinic as a serotonin receptor antagonist for treatment of psychiatric disorders (Barone et al., 1986) and has recently generated interest as a lead DGKot inhibitor for drug repurposing to treat cancer (Boroda et al, 2017; Purow, 2015). DGKot-HEK293T soluble proteomes were treated with ritanserin or ketanserin (100 μΜ compounds, Figure 2B) followed by labeling with ATP acyl phosphate and quantitative chemical proteomics analysis (Figure 4A). Ritanserin concentrations were chosen to provide -70% blockade of DGKot activity as determined from substrate- (Figure 3 A) and chemical proteomic-assays (Figure 3B). Probe-modified peptides showing high competition, as judged by SILAC ratios, were identified as ritanserin binding sites in DMSO/ritanserin comparisons (SR > 5, Figure 6 A and Table 1 and 1A.

These criteria were used to discover that ritanserin inhibits DGKot predominantly through binding interactions at the CI (K237, SR = 7.0) and DAGKa sites (K539, SR = 7.0; Figure 6B and Table 1 and 1A). Surprisingly, minimal competition at the DAGKc domain was observed (K377, SR = 2.0; Table 1 and 1A). Ritanserin competed at common (DAGKa) as well as distinct binding sites (CI) compared with ATP substrate (Table 1 and 1A). The unusual binding mode of ritanserin identified from the LC-MS studies may help explain previous kinetic assays describing a mixed competitive mechanism of inhibition for this inhibitor; ritanserin is hypothesized to bind a DGKot -ATP complex through an unidentified binding site (Boroda et al., 2017). It is proposed that CI could be a potential site mediating ritanserin binding to DGKot distinct from the ATP pocket. Inhibitor profiling of other DGKs revealed that ritanserin showed minimal activity against other isoforms (SR < 2 at all binding sites detected, Figure 6A and Table 1 and 1A). Ritanserin competition was specific because treatment with the negative control probe ketanserin resulted in negligible competition at all probe-binding sites with the exception of a lower SILAC ratio for DGKK peptide, which indicates a potential activating effect for this isoform (Figure 6A and Table 1 and 1A).

One of the advantages of using chemical proteomics is the ability to simultaneously evaluate on- and off-target activity of inhibitors directly in cell proteomes (Chang et al., 2015; Nagano et al., 2013). Here, the selectivity of ritanserin was measured against >50 native kinases quantified in HEK293T soluble proteomes (Figure 7A). On average, >200 probe-modified peptides were detected from -85 protein and lipid kinases per individual SILAC sample. The kinome coverage is comparable with previous reports using ATP acyl phosphates and data-dependent MS scan modes (Patricelli et al., 2007). Native kinases reported in Figure 7A and Table 1 and 1A were quantified in at least 2 biological replicates across all treatment conditions and competed by treatment with free ATP (SR > 5, Table 1 and 1A). The latter criterion (i.e. ATP competition) was important for identifying non- specific probe labeling events in the studies (see Materials and Methods for more details). Kinase targets of ritanserin were defined as those active site peptides that showed SILAC ratios > 5. Based on this criterion, the most potent targets of ritanserin were DGKot and the non-receptor tyrosine protein kinase FER (Greer, 2002) (SR = 7.9; Figure 7A and B). It was confirmed that ritanserin was competing at ATP binding sites of FER by demonstrating potent competition at the same site (K591) with free ATP (SR = 19.3, Table 1 and 1A). Collectively, the studies demonstrate the use of chemical proteomics to elucidate the binding mode and selectivity of ritanserin, resulting in discovery of the CI domain as a novel ligand binding site and FER as an unanticipated off-target.

Discovery of a lead fragment inhibitor of DGKot by ritanserin deconstruction.

In an effort to improve selectivity of ritanserin for DGKot, ligand deconstruction (Hajduk et al., 2000; Kozakov et al., 2015; Lingel et al., 2017) strategies were explored to evaluate the contributions of representative fragments for binding affinity and selectivity. It was hypothesized that the 4-substituted piperidine moiety of ritanserin (highlighted in red, Figure 7C) is a likely

pharmacophore required for DGKot inhibition because of conservation of this motif across several DGKot inhibitors (Boroda et al., 2017) (Figure 10E). Here, the capacity of quantitative chemical proteomics was tested to evaluate binding mode and selectivity of a ritanserin fragment (designated RFOOl, Figure 7C) against recombinant DGKs and endogenous kinases directly in native cell proteomes.

It was confirmed that RFOOl blocked DGKot activity in a concentration-dependent manner using the DAG phosphorylation substrate assay (IC50 = 223 μΜ, Figure 7C). The data show substantially lower potency of RFOOl compared with ritanserin (~ 10-fold difference in IC50 values when comparing Figure 3A and 7C), which is expected of low molecular weight fragments (<300 Da) that typically exhibit binding affinities in the high micromolar to millimolar range (Erlanson et al., 2016). To account for differences in potency, RFOOl was tested at 10-fold higher concentrations (1 mM) in the subsequent LC-MS assays. This concentration of RFOOl was chosen to provide >80% inhibition of DGKot activity in the probe-binding assay (Figure 12). Akin to ritanserin, RFOOl treatment resulted in potent competition at CI (SR = 12.6) and DAGKa sites (SR = 9.1) while showing weak activity at the DAGKc site (SR = 1.7, Figure 7D and Table 1 and 1 A). It was also confirmed that RFOO 1 was largely inactive against other DGK subtypes as determined by low SILAC ratios at all detected DGK probe-modified sites (average SR ~1, Figure 7A and Table 1 and 1A). The similar inhibition profiles of RFOOl and ritanserin observed in the LC-MS analyses support that the ritanserin binding mode is conserved with the ritanserin fragment and that the 4-substituted piperidine group represents a core binding motif of DGKot inhibitors.

While ritanserin and RFOOl share similar inhibition profiles within the DGK family, they differed substantially in cross-reactivity against the kinome. A striking finding from the studies is the dramatic improvement in selectivity against the kinome observed with RFOOl compared with ritanserin (Figure 7A). Specifically, the potent FER off-target activity observed with ritanserin was largely eliminated using RF001 (SR = 1.2, Figure 7B). In fact, RF001 showed potent activity (SR >_5) against a single kinase target, DGKot, across all detectable kinases (native and recombinant DGKs) quantified in the chemical proteomics studies (Figure 7A and Table 1 and 1A). Closer inspection of the data revealed that unlike ritanserin, RFOO 1 maintained good selectivity even for kinase targets that show moderate to weak inhibitory activity (25 versus 3 kinase targets that show SR >_2 for ritanserin versus RFOOl, respectively; Figure 7E).

Discussion

ATP acyl phosphates and quantitative LC-MS were used to map ligand-binding regions corresponding to the active site of mammalian DGKs. It was defined, for the first time, the location of the ATP binding site of representative isoforms from all five principal DGK subtypes (Figure 5). Inspection of the DGK ATP binding sites reveals several features that are unique to this lipid kinase family. First, ATP -sensitive, probe-modified peptides were identified from both DAGKc and DAGKa subdomains, supporting interactions between these regions within the catalytic domain to constitute a potential ATP binding cleft. Crystal structures of soluble bacterial lipid kinases with homology to mammalian DGKs have also been found with active sites located in an interdomain cleft (Bakali et al., 2007). The finding that the DAGKa region is involved in substrate binding was important for assigning a catalytic role to this domain and helps explain previous reports that C-terminal truncations impair DGK enzymatic activity (Los et al., 2004). Second, conserved sequences corresponding to ATP binding sites of DGKs (Figure 5B and C) are not homologous with glycine-rich loops mediating ATP binding of protein kinases (Hanks et al., 1988; Hemmer et al., 1997). The data provide the first experimental evidence in support of a unique DGK ATP binding motif that was postulated over 20 years ago (Schaap et al., 1994). Finally, it is speculated that detection of a single ATP binding site (as opposed to 2 sites in other DGKs) for DGKK and DGKs is a reflection of functional differences in substrate binding of DGK subtypes (Figure 5A). In support of this hypothesis, DGKK, along with other type 2 members, contain an unusual peptide motif that physically separates the DAGKc and DAGKa subdomains (Imai et al., 2005). DGKs, the sole type 3 member, is the only subtype that lacks regulatory domains and shows acyl chain preference in DAG substrate assays in vitro (Tang et al., 1996). It is noted that DGKK and DGKs showed lower recombinant protein expression compared with other isoforms (Figure 8) and so one cannot rule out the possibility of detection limits using the LC- MS approach.

Clues to domain binding sites of DGKs and how to exploit these regions for development of DGKot -selective inhibitors were also discovered. The identification of a probe-modified site at CI domain provided the first evidence of a ligand binding site remote from the ATP binding region of DGKs. Although one cannot rule out the possibility of alternative mechanisms, e.g. probe binding due to domain- (Nordin et al., 2015) or protein-interactions (Okerberg et al., 2014), evidence is provided that the CI domain serves as a ligand binding site for ritanserin distinct from the ATP binding region of DGKa (Figure 5 A and 6A). The overlapping (DAGKa) and distinct (CI) binding sites of ritanserin compared with ATP helps explain previous kinetic findings of a mixed competitive mechanism of inhibition whereby ritanserin prefers to bind a DGKot-ATP complex (Boroda et al., 2017). It was investigated how the binding mode of ritanserin affects selectivity against other DGK isoforms as well as >50 native kinases detected in cell proteomes. While ritanserin showed good selectivity within the DGK superfamily, discovered substantial cross-reactivity against protein kinases was discovered, including the non-receptor tyrosine kinase FER that was inactivated to a similar magnitude as DGKa (SR = 7.9, Figure 7A and B). An unexpected finding was the discovery that a ritanserin fragment (RFOOl) functioned as a DGKa inhibitor that retained binding at CI and DAGKa sites (Figure 7D) and largely removed FER and other kinase off-target activity (Figure 7A and E). Conservation of fragment binding mode is characteristic of ligand-binding hotspots (Hall et al., 2015; Kozakov et al., 2015) of proteins suitable for fragment-based lead and drug discovery (Erlanson et al., 2016).

Conclusion

The studies describe the first functional proteomic map of ligand-binding regions that mediate substrate (ATP) and inhibitor binding in the poorly annotated active site of the mammalian diacylglycerol kinase (DGK) superfamily. Given the dearth of lipid kinase inhibitors available in the clinic and the emerging role of DGKs as anticancer and immunotherapy targets, it is believed that the findings offer new prospects for chemical probes to study and target lipid kinases. It is defined, for the first time, the location of the ATP binding site of representative isoforms from all five principal DGK subtypes (type 1 - 5). Inspection of DGK ATP binding sites identify conserved features that are distinct from protein kinases, providing the first experimental evidence in support of a DGK-specific ATP binding motif that was postulated over 20 years ago. Clues to domain regions of DGKs important for inhibitor development were discovered by identifying probe-modified sites in CI and accessory (DAGKa) domains that serve as primary binding sites for the DGKa inhibitor ritanserin.

An unexpected finding was the discovery that a fragment of ritanserin (RFOOl) functioned as a DGKa inhibitor that retained binding at CI and DAGKa domains and largely removed protein kinase off- target activity. While few examples have been reported, conservation of fragment binding mode is characteristic of ligand-binding hotspots of proteins suitable for fragment-based lead discovery. Thus, it is believed that the CI and DAGKa sites are key binding regions of DGKs to enable development of high affinity, isoform-selective inhibitors of this lipid kinase superfamily.

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Example 2

Ritanserin is a CRAF Inhibitor with Cytotoxicity against Small Cell Lung Cancer Cells

Introduction

Ritanserin is a serotonin (5-hydroxytryptamine, 5-HT) receptor antagonist with specificity for the 5-HT2 subtype (Leysen, 1985). As a drug candidate, ritanserin was tested for treatment of several neuropsychiatric disorders but never received approval for clinical use (31). The oral bioavailability (~40-hour half-life) and lack of adverse side effects in humans has since prompted studies to explore ritanserin for clinical applications beyond serotonin signaling (Purow, 2015). For example, ritanserin was discovered to function as a diacylglycerol kinase-alpha (DGKa) inhibitor, which shifted focus towards use of this compound for modulation of lipid signaling in cancer (Boroda, 2017; Purow, 2015) (Figure 14). As demonstrated herein, quantitative chemical proteomics was used to evaluate ritanserin selectivity against the kinome and it was discovered that the non-receptor tyrosine protein kinase FER is an additional potent target (Franks, 2017). Epidermal growth factor receptor (EGFR) signaling activates FER resulting in phosphorylation and activation of the guanine nucleotide exchange factor (GEF) Vav2 to enhance cell migration, invasion, and tumor metastasis of lung cancer cells (Ahn, 2013). Thus, ritanserin is capable of disrupting lipid and protein pathways mediating oncogenic signaling and can serve as a useful candidate for targeting broad tumor cell types. Here, ritanserin cytotoxicity and kinome-wide selectivity in lung cancer cells that differed by subtype and mutational status is evaluated.

Materials and Methods

Materials. Desthiobiotin ATP acyl phosphate nucleotide probe was obtained from

ThermoFisher Scientific (PI88311). Ritanserin and ketanserin tartrate were purchased from Tocris Bioscience. WST-1 reagent kits were purchased from Cayman Chemical. Trypan Blue was purchased from ThermoFisher Scientific. CaspaseGlo Assay kits were purchased from Promega.

WST-1 Cell Proliferation Assays. Tumor cells were plated in transparent tissue-culture treated 96-well plates at a density of 100,000 cells/mL (A549, H1650) or 200,000 cells/mL (H82) in a volume of 100 per well. Cells were treated with dimethyl sulfoxide (DMSO) vehicle or inhibitors dissolved in DMSO at the indicated concentrations (final DMSO concentration of 0.5%). Cells were allowed to grow for indicated times at 37 °C under 5% CO ₂ . Afterwards, equal parts of WST-1 developer reagent and electron mediator solution were mixed and 10 of the resulting solution ('WST-1 reagent') were added to each well. Plates were shaken in an orbital shaker for 60 s and then returned to the incubator for two hrs. Plates were again shaken followed measurement of absorbance at 450 nm. Data were normalized to DMSO-treated wells and significance values determined with one-way ANOVA.

Cell Counts. Tumor cells were plated in 60 mm plates at a density of 100,000 cells/mL (A549, H1650) or 200,000 cells/mL (H82) and a volume of 3.5 mL/plate. Cells were treated with inhibitors at the indicated concentrations (final DMSO concentration of 0.5%) for 48 hrs at 37 °C under 5% CO2. After incubation, adherent cells were washed and detached with trypsin and all cells were collected and concentrated by spinning at 400 x g for 3 min followed by aspiration of media. Cells were resuspended in 10 nM Trypan Blue and 10 of this solution counted via a

hemocytometer. Dead cells were excluded from all counts. Data were normalized to DMSO-treated wells and significance values determined with one-way ANOVA.

Caspase Glo Assays. Assays were performed as directed by the manufacturer (Promega). Briefly, tumor cells were plated in black tissue-culture treated transparent-bottom 96 well plates at a density of 200,000 cells/mL (A549, H1650) or 400,000 cells/mL (H82) in a volume of 50 nL/well. Cells were treated with inhibitors at the indicated concentrations (final DMSO concentration of 0.5%) for 24 hrs at 37 °C under 5% C0 ₂ . Afterwards, 50 of the prepared CaspaseGlo reagent was added to each well. The reaction was allowed to proceed at 37 °C under 5% CO ₂ for 1 hr, at which point the cells were shaken in an orbital shaker at 500 rpm for 60 s and then luminescence was read for each well. Data were normalized to DMSO-treated wells and significance values determined with one-way ANOVA. LC-MS analysis of SILAC samples using ATP acyl phosphates. Quantitative chemoproteomics was performed as previously described (Franks et al, 2017; McCloud et al., 2018).

Computational Methods. Data for A549 and H82 cell lines were searched with IP2 and manually validated using the methods previously described (Franks et al., 2017). Data for

Desthiobiotin-tagged ATP acyl-phosphate probes and ATP competitive peptides were compared and clustered. Ritanserin and ketanserin inhibition profiles were compared using SILAC ratios and normalized to DMSO. The kinase profiles were displayed as a heatmap and clustered with hierarchical clustering using R package d3heatmaps (blog.rstudio.org/2015/06/24/d3heatmap/) as previously described (Franks et al., 2017).

Lipid kinase phylogenetic tree. Phylogenetic tree of human lipid kinases was generated using

MUSCLE multiple sequence alignment (Edgar, 2004) of annotated lipid kinases and a least squared distance method for determining evolutionary distance. Calculations were conducted using the EMBOSS software suite (Rice et al., 2000).

Statistical analysis and determination of IC50 values. For all cell viability measurements, results were normalized to values obtained from DMSO treated cells. For CaspaseGlo assays, raw luminescence values are reported. All significance values for Cell Viability and CaspaseGlo assays were calculated with one-way ANOVA. All statistical analyses were performed using GraphPad Prism.

Results and Discussion

Ritanserin mediates apoptotic cell death of lung cancer cells independent of serotonin signaling

Cell viability assays were conducted to determine the impact of ritanserin treatments on survival of NSCLC and SCLC cells. H1650 and A549 were chosen as the non-small cell lung cancer (NSCLC) cell models to compare sensitivity of cells with different gene mutations to ritanserin exposure. HI 650 express EGFR receptors contain activating mutations in the kinase domain (exon 19 deletion E746-A750 (Irmer, 2007 #4631)) of this receptor tyrosine kinase. A549 cells express wild- type EGFR but harbor mutant KRAS (G12S)(Kharbanda, 2014). H82 cells (Jahchan, 2013) were also included in the studies to evaluate ritanserin activity in small cell lung cancer (SCLC). Ketanserin (Franks, 2017; Boroda, 2017) was used alongside ritanserin to control for potential 5-HT ₂ R activity and other non-specific pharmacological effects in cell biology. Cells were treated with varying ritanserin concentrations (5-50 μΜ) and cell viability measured using established WST-1 metabolic assays (Kepp, 2011). Concentration-dependent decreases in viability in cells exposed to ritanserin but not ketanserin treatments was observed (Figure 15 A, Figure 18A and B). At a moderate concentration of ritanserin (25 μΜ), >70% inhibition of cell growth across all NSCLC and SCLC lines exposed to compound was observed (Figure 15A). At lower concentrations (5 μΜ), ritanserin showed enhanced cytotoxicity against the SCLC H82 (-50% cell death) cells compared with NSCLC cells (-5-15% cell death across A549 and H1650 cells, Figure 15A). Cell killing with ritanserin was rapid with >50% of cell death occurring after 1 day and near-maximal cytotoxicity after 2 days of treatment in all cell lines (25 μΜ dose, Figure 15B). The lack of activity using ketanserin under the same treatment conditions further supports that ritanserin-mediated cytotoxicity of lung cancer cells is not due to antagonism of 5-HT2R receptors (Figure 15, Figure 18A and B). In contrast to pan-kinase inhibitor staurosporine, which showed general cytotoxicity across all cells tested (Figure 15B and Figure 18C), ritanserin showed negligible cell killing against noncancerous primary cells even at the highest concentration tested (50 μΜ, Figure 19C). Collectively, the results demonstrate that ritanserin is not generally cytotoxic but displays potent cell killing of NSCLC and SCLC cells.

Since changes in cell metabolism can occur from non-lethal perturbations (Kepp, 2011), live cell counts were used to further support cytotoxicity of lung cancer cells with ritanserin treatments

(Figure 16A). Akin to results from cell viability assays, significant cell killing was observed across all lung cancer cell lines exposed to ritanserin but not ketanserin (Figure 16A). Potent cell killing (-70%) was observed even at the lower dose tested (10 μΜ, Figure 16A). Next, caspase activity was measured in treated cells to determine whether ritanserin mediates cell killing through activation of apoptosis. Cells treated with ritanserin showed significantly enhanced caspase 3/7 activity after 24 hours compared with vehicle controls (Figure 16B). Caspase activation by ritanserin was specific because ketanserin treatments under the same experiments conditions did not induce these effects (Figure 16B). Ritanserin effects were compared directly with staurosporine, which has been show in previous reports to activate apoptosis in lung cancer cells (Bartling, 2004; Wang, 2009). In both HI 650 and H82 cells, comparable activation of caspase 3/7 compared with staurosporine was observed (Figure 16B). While ritanserin treatment of A549 cells resulted in a lower degree of activation, the increase in caspase 3/7 was significant compared with vehicle and ketanserin treated cells (Figure 16B). In summary, the cell viability and caspase activation data support ritanserin induction of apoptotic cell death against lung cancer cells that differ in mutation status (EGFR, KRAS) and subtype (NSCLC vs SCLC).

Chemical proteomics to elucidate ritanserin targets in NSCLC and SCLC cell proteomes

Based on previous chemical proteomics (Franks, 2017), it was hypothesized that ritanserin is functioning as a kinase inhibitor to mediate cytotoxicity in the lung cancer cell models. Since A549 and H1650 displayed similar sensitivities to ritanserin in the cell viability assays, A549 and H82 were selected for chemical proteomic evaluation of ritanserin targets in NSCLC and SCLC proteomes, respectively. To test this hypothesis, desthiobiotin-tagged, ATP acyl-phosphates (Patricelli et al., 2011; Patricelli et al., 2007) were used to measure selectivity of compounds against native kinases detected in lung cancer proteomes. ATP acyl-phosphate probes permit global profiling of kinase activities by covalent attachment of reporter tags to conserved lysines in the ATP binding site of protein lipid kinases as well as other ATP -binding proteins (Patricelli et al., 2011; Patricelli et al.,

2007). For these studies, NSCLC and SCLC cells were cultured in isotopically light and heavy amino acids to enable quantitative chemical proteomics (Chang, 2015) by stable isotope labeling with amino acids in cell culture (SILAC, Figure 17A). Light and heavy cell proteomes were treated with DMSO vehicle or compound, respectively, prior to addition of ATP acyl phosphate to label active site lysines. After probe labeling, light and heavy proteomes were combined, digested with trypsin protease, and desthiobiotin-modified peptides enriched by avidin affinity chromatography and analyzed by LC- MS/MS to identify and quantify isotopically tagged active-site peptides from native kinases as previously described(Franks, 2017) (Figure 17A).

Using quantitative chemical proteomics assay described herein, kinase activity profiles between A549 and H82 cell proteomes were compared. Kinases included in the comparisons were quantified across at least 2 biological replicates and showed potent competition with free ATP (SR > 5, Figure 17A). The latter criterion was used to distinguish specific probe binding at ATP -binding sites versus non-specific labeling of surface lysines. Hierarchical clustering of the over 120 kinases separated into three distinct groups: overlapping, enriched for NSCLC and enriched for SCLC subtypes (Figure 17A). Specifically, activity-dependent enrichment of several kinases was observed (AKT 1/2/3 and IKKA) in A549 proteomes that is consistent with enhanced PI3K/AKT signaling in NSCLC subtypes containing KRAS mutations (Castellano, 2013) (Figure 17A). A similar analysis of SCLC kinase profiles reveals enrichment of kinases involved in RAF signaling as well as the DNA damage response (Figure 17A). In particular, the abundance of probe -modified active site peptides of CRAF was ~3 fold higher in H82 compared with A549 cell proteomes (Figure 17B). These findings support previous observations that CRAF is one of several proto-oncogenes that are highly expressed in SCLC cells and tumor tissues (Graziano, 1991). Collectively, the kinase activity-based profiling studies reveal differences in signaling pathways that differentiate NSCLC and SCLC subtypes.

Next, ATP probe assay was used to determine the kinase targets of ritanserin in A549 and H82 proteomes (Figure 17). Ketanserin was included in the LC-MS studies to discern ritanserin- specific from general non-specific activity of 5-HT ₂ R antagonists against the kinome. The rationale for choosing to test a drug concentration (100 μΜ) 10-fold higher than required for potent cell killing (10 μΜ, Figure 16A) is to account for potential shifts in potency of reversible inhibitors due to irreversible labeling kinetics of ATP acyl phosphate probe (Patricelli, 2011). Kinase targets of ritanserin were defined as those active site peptides that showed SILAC ratios > 5. Based on this criterion, the most potent targets of ritanserin were FER, TLK2 and CRAF (Figure 17). FER was identified as a potent target of ritanserin in previous chemical proteomic studies (Franks, 2017).

Filtering by a three-fold change cutoff show BRAF inhibition by ritanserin. The combined inhibition of both RAF proteins suggests a mechanism for cancer cell cytotoxicity and presents the possibility of ritanserin treatment overcoming paradoxical CRAF activation in response to BRAF inhibition (Holderfield et al., 2013 Cancer Cell). It was confirmed that ritanserin was competing at ATP binding sites of target kinases by demonstrating potent competition at the same sites with free ATP. Discovery that ritanserin is a direct inhibitor of RAF 1 catalytic activity

To further confirm that ritanserin is a CRAF inhibitor, a targeted parallel reaction monitoring method (PRM) was developed to evaluate compound activity against CRAF and other members of the RAF family (ARAF and BRAF). Targeted PRM was needed because of the low abundance of CRAF compared with ARAF and BRAF). Using the PRM approach, it was confirmed that ritanserin shows potent activity against CRAF with negligible activity against ARAF and BRAF in H82 proteomes (Figure 17D). Ritanserin activity was also measured against RAF kinases in A549 proteomes using the targeted LC-MS method. It was found that one could not detect CRAF in A549 proteomes despite using a more sensitive LC-MS approach. The data further support previous findings that this RAF member is enriched in SCLC cells (REF). Collectively, it was confirmed that by using more sensitive LC-MS methods that ritanserin shows enhanced potency against CRAF among the RAF family of kinases.

Given the potential for indirect inhibitory effects in the competition studies in lysates, ritanserin activity was tested in a CRAF substrate assay. Ritanserin inhibition was measured against recombinant RAF1 using commercial substrate assays. These studies were validated the chemical proteomic findings by demonstrating that ritanserin could block RAFl catalytic activity. RAF1 was overexpressed in HEK293T cells and measured recombinant RAF 1 activity by comparing with non- transfected HEK293T (i.e. mock) proteomes. An increase was observed in RAF1-HEK293T compared with mock proteomes, which was specific because heat denaturation reduced activity back to mock levels. Pretreatment with ritanserin but not ketanserin resulted in concentrations dependent blockade of recombinant RAFl activity. In summary, the results confirm agreement between chemical proteomics and biochemical substrate assays that ritanserin is a RAFl inhibitor.

Conclusion

Ritanserin was tested in the clinic as a serotonin receptor (5-HT2R) antagonist but recently emerged as a novel kinase inhibitor with potential applications in cancer. Here, it is shown that ritanserin treatment induced apoptotic cell death of non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) but not noncancerous cells. Treatment with a structurally analogous 5-HT2R antagonist ketanserin did not impact cell viability, supporting a ritanserin-specific and serotonin- independent effect. Chemical proteomics and quantitative mass spectrometry was used to identify putative kinase targets of ritanserin across the lung cancer kinome. Correlation of target engagement profiles with cytotoxicity resulted in discovery of CRAF as a putative target to explain enhanced sensitivity of SCLC cells to ritanserin treatment. Substrate assays using recombinant CRAF confirmed that ritanserin is a direct inhibitor of this oncogene. Thus, ritanserin has use as a drug repurposing in cancer. Novel activity of ritanserin in diverse lung cancer types segregated by type and mutation status has been shown. Provided herein is evidence that ritanserin functions as a kinase inhibitor with broad action against diverse lung cancer types. Ritanserin is identified as a novel inhibitor of RAF kinases with enhanced potency for RAF 1.

Example 3

[A] Labeling HEK293T cell proteomes to determine target proteins of JWB003 in vitro

1. HEK293T cells were harvested in cold PBS.

a. Cells were transferred to Eppendorf tube .

2. Cells were lysed via tip sonicator.

3. Cells were fractionated into membrane and soluble fraction.

a. 100,000xG for 45 minutes at 4 degree.

b. Supernatant was separated from cell pellet.

4. Dilute proteomes to 1 mg/mL in PBS and aliquot appropriate reaction volume (49 for probe only; 48 for competition + probe)

5. Cells were treated with 5 OX inhibitor.

a. Incubated for lHr at 37 degree.

6. Cells were treated with 50X Probe (JWB003).

a. Incubated for lHr at 37 degree.

7. Add 6 of master mix to each alkyne probe -labeled sample.

a. 1 of 1.25 mM Rh-N ₃

b. Ι μΙ, of fresh 50 mM TCEP

c. 3 μί of 1.7 mM TBTA stock

d. 1 μΕ οί 50 ηιΜ Οι80 ₄

8. Vortex samples.

9. Incubate at room temperature for 1 hr

10. Quench with 17 μΐ, of 4X SDS-PAGE loading buffer + βΜΕ and vortex tubes.

1 1. Analyze 30 μί _^ samples by SDS-PAGE immediately.

[B] Labeling HEK293T cells to determine target proteins of JWB003 in live cells (in situ)

1. Complete media was removed from HEK293T cells and replaced with serum free media containing JWB003 at the appropriate final concentration

a. Cells were placed in incubator for appropriate time at 37 degree 5% CO ₂

2. Cells were washed

a. 2x warm PBS

b. 2x cold PBS

c. Harvest cells in cold PBS

3. Cells were transferred to Eppendorf tube

4. Cells were lysed via tip sonicator

5. Cells were fractionated into membrane and soluble fraction a. 100,000xG for 45 minutes at 4 degrees

b. Supernatant was separated from cell pellet.

6. Dilute proteomes to 1 mg/mL and aliquot appropriate reaction volume (50 μΚ)

7. Add 6 of master mix to each alkyne probe-labeled sample.

a. 1 μί. of 1.25 mM Rh-N ₃

b. Ι μΙ, of fresh 50 mM TCEP

c. 3 of 1.7 mM TBTA stock

d. 1 μΕ οί 50 ηιΜ Οι80 ₄

8. Vortex samples.

9. Incubate at room temperature for 1 hr.

10. Quench with 17 μΐ, of 4X SDS-PAGE loading buffer + βΜΕ and vortex tubes.

1 1. Analyze 30 μί _^ samples by SDS-PAGE immediately.

[C] Screening activity of compounds against target kinases using a JWB003 live cell labeling assay

1. Complete media was removed from HEK293T cells and replaced with serum free media containing inhibitor or DMSO at the appropriate final concentration

a. Cells were placed in incubator for lHr at 37 degree 5% C02

2. Cells were treated with JWB003 ( 1000X stock)

a. Cells were placed in incubator for lHr at 37 degree 5% C02

3. Cells were washed

a. 2x warm PBS

b. 2x cold PBS

c. Harvest cells in cold PBS

4. Cells were transferred to Eppendorf tube

5. Cells were lysed via tip sonicator

6. Cells were fractionated into membrane and soluble fraction

a. 100,000xG for 45 minutes at 4 degrees

b. Supernatant was separated from cell pellet.

7. Dilute proteomes to 1 mg/mL and aliquot appropriate reaction volume (50 μί)

8. Add 6 μΐ _^ of master mix to each alkyne probe-labeled sample.

a. 1 μί of 1.25 mM Rh-N ₃

b. Ι μΙ, of fresh 50 mM TCEP

c. 3 μί of 1.7 mM TBTA stock

d. 1 μΕ οί 50 ηιΜ Οι80 ₄

9. Vortex samples.

10. Incubate at room temperature for 1 hr. 1 1. Quench with 17 μί of 4X SDS-PAGE loading buffer + βΜΕ and vortex tubes.

12. Analyze 30 samples by SDS-PAGE immediately.

[D] Labeling HEK293T cell proteomes to determine target proteins of JWB017 in vitro

1. HEK293T cells were harvested in cold PBS

a. Cells were transferred to Eppendorf tube

2. Cells were lysed via tip sonicator

3. Cells were fractionated into membrane and soluble fraction

a. 100,000xG for 45 minutes at 4 degree

b. Supernatant was separated from cell pellet.

4. Dilute proteomes to 1 mg/mL and aliquot appropriate reaction volume (49 for probe only;

48 for competition + probe)

5. Cells were treated with 50X Probe (JWB003)

a. Incubated for appropriate time point at 37 degree

6. Add 6 μΐ _^ of master mix to each alkyne probe-labeled sample.

a. 1 μί of 1.25 mM Rh-N ₃

b. Ι μΙ, of fresh 50 mM TCEP

c. 3 μί of 1.7 mM TBTA stock

d. 1 μΕ οί 50 ηιΜ Οι80 ₄

7. Vortex samples.

8. Incubate at room temperature for 1 hr.

9. Quench with 17 μΐ, of 4X SDS-PAGE loading buffer + βΜΕ and vortex tubes.

10. Analyze 30 μί _^ samples by SDS-PAGE immediately.

[E] JWB017 fluorescent polarization assay for high-throughput screening (HTS) of purified rat DGKa

1. Rat DGKa was diluted to 1 mg/ml in buffer (50mM Tris 8.0, 150mM NaCL, and 0,01%

Pluronic F-127)

2. 9 μί _^ οΐ 4uM of purified rat DGKa was aliquoted into 384 well plate (7 well)

3. \ μί _^ of DMSO or 10X probe was added to each well

4. Incubate at room temperature for appropriate time point

5. Read Fluorescence polarization

Synthesis of RF001

tert-butyl 4-(bis(4-fluorophenyl)(hydroxy)methyl)piperidine-l-carboxyla te

Molecular Weight: 403.4698

1. 1-Boc isonipecotic acid ester ( 1 eq) was dissolved in anhydrous THF and cold to 0 degree a. 4-fluorophenylmagnesium bromide (2.5 eq) was added dropwise via syringe

2. Flask allowed to warm to room temperature and stirred overnight

3. Reaction as quenched with saturated ammonium chloride

a. Extract in EtOAC

b. Wash with sodium bicarbonate

c. Wash with brine

4. Concentrated on rotary evaporator

5. Triturated several times with Cold EtOAC and hexanes

a. Collected final product as white solid

RF001

1. tert-butyl 4-(bis(4-fluorophenyl)(hydroxy)methyl)piperidine-l -carboxylate

a. Dissolved in 1 : 1 mix of DCM and Trifluoroacetic acid

i . Stir at room temperature for two hours

b. Concentration on rotary evaporate

6. Triturate several times with Triturated several times with Cold EtOAC and hexane

JWB003

(E)-4-(4-(2-((tert-butoxycarbonyl)amino)ethyl)piperazin-l-yl )but-2-enoic acid

1. tert-butyl (2-(piperazin-l-yl)ethyl)carbamate ( 1.1 eq) was dissolved in THF

a. Diisopropyl ethyl amine (eq) was added

2. (E)-4-bromobut-2-enoic acid ( 1) was dissolved in THF and added to reaction flask

3. Flask was allowed to stir overnight

4. Sample was concentrated via rotary evaporator and carried on to next step without further purification. tert-butyl (E)-(2-(4-(4-(4-(bis(4-fluorophenyl)methylene)piperidin-l-yl )-4-oxobut-2-en-l- yl)piperazin-l-yl)ethyl)carbamate

1. (E)-4-(4-(2-((tert-butoxycarbonyl)amino)ethyl)piperazin-l -yl)but-2-enoic acid (leq) was dissolved in 2ml of anhydrous DMF.

2. HATU (2.2eq) was added to the reaction flask and allowed to stir for one minute

3. RFOO l ( 1.5eq) and DIEA (3eq) were dissolved in anhydrous DMF and added to the reaction flask

4. Reaction was allowed to stir overnight

5. Reaction was concentrated on rotary evaporator.

6. Purified via column chromatography 5-10% methanol in dichloromethane

JWB003

1. Reaction was dissolved in 4M HCl/dioxanes for two hours

2. Reaction was dried on rotary evaporator.

3. pent-4-ynoyl bromide (1.5 eq) was dissolved into THF with DIEA (3 eq)

4. Reaction was allowed to stir overnight

5. Reaction was washed quenched with sodium bicarbonate

a. Extracted into ethyl acetate

b. Washed with brine

6. Sample was dried over magnesium sulfate

7. Concentrated on rotary evaporator

8. Sample was purified via RP-HPLC

JWB019

(2E)-4-Bromobut-2-enoic Acid Chloride

1. (2E)-4-Bromobut-2-enoic Acid (1 eq) was dissolved in anhydrous THF

2. Thionyl chloride (1.5 eq) was added dropwise to the reaction flask

a. Catalytic drop of DMF was added to the reaction flask

3. Reaction stirred for 3 hour at RT

4. Concentration on rotary evaporation

5. Carry to next step without further purification

JWB018

1. RF001 ( 1 eq) was dissolved in anhydrous THF

a. Triethyl amine (3 eq) was added to flask

b. Sample was cooled to -20 degree

2. (2E)-4-Bromobut-2-enoic Acid Chloride ( 1.3 eq) was dissolved in anhydrous THF

a. Add dropwise over 15 minutes

b. Allowed to stir at -20 degree for 30 minutes

3. Reaction was quenched with sodium bicarbonate

a. Extracted in ethyl acetate

b. Washed with brine

c. Dried with magnesium sulfate

4. Concentrate on rotary evaporator

5. Purified via column chromatography ( 1 :3 ethyl acetate : hexane s)

1. JWB018 (1 eq) was dissolved in THF

a. Cooled on ice

2. Propargyl amine (1.5 eq) was dissolved In THF with DIEA (3 eq) and added to the reaction flask slowly.

3. Reaction was allowed to warm to room temperature and stirred overnight

4. Reaction was quenched with sodium bicarbonate

a. Extracted in ethyl acetate

b. Washed with brine

5. Concentrated on rotary evaporator

6. Purified via column chromatography (2% methanol in DCM) PROBE UTILITY: For example, JWB003 is a cysteine reactive covalent probe that broadly targets CI -domain containing proteins and may be used to study the lipid response and activity of protein and lipid kinases. As another example, JWB017, a rhodamine analog of JWB003, can be used to discover new inhibitors of CI domain proteins through fluorescent polarization high throughput screening (HTS) assays.

JWB003 covalently labels hDGKa in situ. Time dependent labeling of HEK293T cells transiently transfected with recombinant hDGKa shows time dependent labeling with JWB003 at 25 μΜ with prominent labeling in the membrane fraction of cell proteome. Probe labeling appears to saturate at 60 minutes.

Competition experiments to support JWB003 labeling of CI domain cysteines of hDGKa in vitro.

Probe labeling is inhibited by CI domain inhibitors such as ritanserin and phorbol esters (PMA), but not catalytic domain inhibitors such as adenosine triphosphate (ATP). JWB003 labeling is inhibited by the general cysteine inhibitor iodoacetamide, giving evidence that the probe covalently modifies cysteine. The sensitivity to PMA and unique ability to label at the CI domain of kinases allows JWB003 to probe lipid activation of lipid kinases including DGKs.

JWB003 labels all ten isoforms of recombinant DGKs in situ. HEK293T cells were transiently transfected to express distinct recombinant DGK isoforms (total of 10). JWB003 treatment shows effective labeling of all ten proteins in live cells. The ability to label all DGK isoforms expands the utility of the probe to study lipid recognition of all ten DGK isoforms.

JWB003 labels protein kinases that contain CI domains. HEK293T cells were transiently transfected to express human PKCa (hPKCa). JWB003 treatment showed labeling of hPKCa in the membrane but not soluble fraction of the cell proteome. The significance of this finding is hPKCa is membrane localized after activation by lipid signals in cell signaling. Data shows that PMA (mimics DAG lipid secondary messengers) activation of hPKCa-HEK293T cells results in prominent hPKCa expression in the membrane, which can be detected by JWB003.

Gel-based activity based protein profiling analysis shows time dependent labeling of purified rat DGKa (rDGKa) using JWB017, a rhodamine analog of JWB003. Gel-based experiments were used to optimize JWB017 labeling conditions of purified rDGKa for fluorescence polarization assay. Data show that -50% labeling of protein was achieved at 60 min.

JWB017 can be used to discover new inhibitors of CI domain proteins through fluorescent polarization high throughput screening (HTS) assays. Fluorescent polarization assay (FluoPol Assay) showing time dependent labeling of pure rat DGKa (rDGKa). When excited with plane-polarized light, fluorophore emit light parallel to the plane of excitation unless it rotates in the excited-state. The speed of molecular rotation results in depolarization. When free in solution, the fluorophore emits depolarized light, but when bound by a protein, the fluorophore rotates much more slowly and emits highly polarized light. Using the parameters optimized in the in-gel assay above, pure rat DGKa was treated to determine if the probe could meet the necessary conditions for a fluorescence polarization assay: (1) probe labeling in the 50-100 nM range, (2) efficient labeling in a reasonable amount of time (0.5-2.0 hours) and (3) labeling of the protein at room temperature. It was determined that enzyme alone does not give appreciable background signals (JWB017 vs DMSO). The fluorescence polarization (FP) signal is observed to be 2-4X higher in JWB017 + rDGKa samples when compared to JWB017 probe alone. Protein labeling was effectively seen with 100 nM of JWB017, optimal labeling is observed at the 60-minute time point, and FP signal is enzyme dependent. In a HTS assay, pretreatment with inhibitor libraries will identify compounds that bind at rDGKa CI domain because they will outcompete JWB017 labeling, which results in lower FP signals. Bibliography

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Example 4

The compounds of the various embodiments can be synthesized as described in the following examples.

JWB002 & JWB003

JWB007

101

102

The disclosure provides for the following additional embodiments and clauses, the numbering of which is not to be construed as designating levels of importance:

Embodiment 1 : A biiunctional inhibitor that incorporates RFOO 1 into its structure to mediate selective blockade of target kinases that contain both a regulatory domain (e.g. C I) and kinase domain in the same protein:

• ritanserin inactivates DGKA through binding of CI and DAGKc site of kinase domain (Franks et al. Cell Chemical Biology 2017)

• ritanserin inactivates FER through binding of kinase domain and a potential additional domain (Franks et al. Cell Chemical Biology 2017)

• ritanserin inactivates CRAF, which contains a C I and kinase domain (Fig. 20)

• RFOO l inactivates DGKA through binding of CI and DAGKc site of kinase domain (Franks et al. Cell Chemical Biology 2017)

• RFOO l inactivates CRAF, which contains a C I and kinase domain (Fig. 20).

Embodiment 2: RFOO l serves as an activator of CHK2 through binding of a protein domain. Embodiment 3 : Ritanserin, RFOO l, and RFOOl analogs are novel anticancer agents for treatment of small cell and non-small cell lung cancer cells.

Embodiment 4: RFOO l is a CRAF (Uniprot P04049) inhibitor through proposed bifunctional inhibitor mechanism.

Clauses

Clause 1. A compound according to formula (I), formula (II), formula (III), formula (IV), or formula (V):

104

(V),

or a pharmaceutically acceptable salt, polymorph, prodrug, or solvate thereof;

wherein:

X is selected from the group consisting of: -CR ¹⁹ R ¹³ -, -NR ³⁵ -;

Y is selected from the group consisting of: -CR ¹² R ²⁰ -, -NR ³⁶ -;

and X is selected from the group consisting of: I , or I ;

Rl p2 p3 p4 p5 p6 p7 p8 p9 p 10 pll p 12 p 13 p 14 p 15 p 16 p 17 p 18 p 19 p20 p21 p22

_R 22 _R 23 _R 24 _R 25 _R 26 _R 27 _R 28 _R 29 _R 30 _R 31 _R 32 _R 33 _R 34 _R 35 _R 36 _R 37 ^ _R 38 independently, are selected from the group consisting of -H, -F, -CI, -Br and substituted or unsubstituted (C ₁ -C ₁₀₀ ) hydrocarbyl.

Clause 2. The compound of clause 1, wherein R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ , R ¹⁰ , p 11 pl2 pl3 pl4 p 15 p 16 p 17 p 18 p 19 p20 p21 p22 p22 p23 p24 p25 p26 p27 p28 p29 p30 p31

R ³² , R ³³ and R ³⁴ , independently, are selected from the group consisting of: substituted or unsubstituted (Ci-Cioo)alkyl, (Ci-Cioo)alkenyl, (Ci-Cioo)alkynyl, (Ci-Cioo)acyl, (Ci-C ₂ o)cycloalkyl, (Ci-C ₂ o)aryl, (Ci- C ₂ o)aralkly, (Ci-Cioo)alkoxy, an amine, or (Ci-Cioo)haloalkyl. Clause 3. The compound of clause 1 or 2, wherein R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , R ⁸ , R ⁹ ,

RIO Pll Pl2 Dl3 pl4 p 15 p 16 p 17 p 18 p 19 p20 p21 p22 p22 p23 p24 p25 p26 p27 p28 p29 p30

R ³¹ , R ³² , R ³³ and R ³⁴ , independently, are selected from the group consisting of: substituted or unsubstituted (Ci-C4o)alkyl, (Ci-C4o)alkenyl, (Ci-C4o)alkynyl, (Ci-C4o)acyl, (Ci-Cio)cycloalkyl, (Ci- Cio)aryl, (Ci-Cio)aralkly, (Ci-C4o)alkoxy, an amine, or (Ci-C4o)haloalkyl.

Clause 4. The compound of any one of clauses 1-3, wherein R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ ,

R8 p9 plO pll pl2 p 13 p 14 p 15 p 16 p 17 p 18 p 19 p20 p21 p22 p22 p23 p 24 p25 p26 p27 p28 p29

R ³⁰ , R ³¹ , R ³² , R ³³ and R ³⁴ , independently, are selected from the group consisting of: -F, -CI, -Br, -CH3, -CF ₃ , -OCF ₃ , -OCH ₃ , -CH ₂ F, -NH ₂ , -NHS02CH ₂ CH ₂ CH ₃ , -CONHCH ₃ , -C(CH ₃ ) ₃ , -NHCH(CH ₃ ) ₂ , - -COC5H11N, -COOH, -OH,

Clause 5. The compound of any one of clauses 1-4, wherein the structure according to formula (I) is selected from the group consisting of:

107

Clause 6. The compound of any one of clauses 1-5, wherein the structure according to formula (II) is selected from the group consisting of:

109

Clause 7. The compound of any one of clauses 1 -5, wherein the structure according to formula (III) is

Clause 8. The compound of any one of clauses 1-5, wherein the structure according to formula (IV) is

Clause 9. The compound of any one of clauses 1-5, wherein the structure according to formula (V) is

Clause 14. A pharmaceutical composition comprising a compound of any one of clauses 1-9 and a pharmaceutically acceptable excipient.

Clause 15. A method for treating cancer comprising administering an effective amount of at least one compound of formula (I), (II), (III), (IV), or (V) according to any one of clauses 1-13 or the pharmaceutical composition of clause 14 to a subject in need thereof.

Clause 16. The method of clause 15, wherein the cancer is selected from the group consisting of liver cancer, lung cancer, intestinal cancer, kidney cancer, brain cancer, prostate cancer, testes cancer, ovarian cancer, breast cancer, pancreatic cancer, melanoma, lymphoma, leukemia, B- cell cancer or a combination thereof.

Clause 17. The method of clause 16, wherein the lung cancer is small-cell lung or non- small cell lung cancer.

Clause 18. A method for treating a neuropsychiatric disorder comprising administering an effective amount of at least one compound of formula (I), (II), (III), (IV), or (V) according to any one of clauses 1-13 or the pharmaceutical composition of clause 14 to a subject in need thereof.

Clause 19. The method of clause 18, wherein the neuropsychiatric disorder is selected from bipolar disorder, depression, schizophrenia and obsessive-compulsive disorder.

Clause 20. A method to active T-cells comprising contacting an inactive T-cell with an effective amount of at least one compound of formula (I), (II), (III), (IV), or (V) according to any one of clauses 1-13 or the pharmaceutical composition of clause 14.

Clause 21. A method to selectively inhibit a kinase comprising contacting the kinase with an effective amount of at least one compound of formula (I), (II), (III), (IV), or (V) according to any one of clauses 1-13 or the pharmaceutical composition of clause 14.

Clause 22. The method of clause 21, wherein the kinase comprises a regulatory domain and a kinase domain in the same protein.

Clause 23. The method or clause 22, wherein the regulatory domain is a CI domain.

Clause 24. A method to method to screen for inhibitors of kinase activity comprising: a) contacting a kinase with a putative inhibitor;

b) contacting the kinase and putative inhibitor of a) with at least one fluorescently labeled compound of formula (I), (II), (III), (IV), or (V) according to any of clauses 1-13; and c) remove any unbound fluorescently labeled compound and then measure fluorescent signals;

wherein a lower fluorescent signal indicates that the putative inhibitor is an inhibitor of kinase activity.

Clause 25. The method of clause 24, wherein the kinase has a CI domain.