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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cyclin-dependent kinase 9 | ||
| Ligand | BDBM307808 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | TR-FRET Kinase Assay | ||
| IC50 | 22.0±n/a nM | ||
| Citation |  Mastracchio, A; Bruncko, M; Lai, C; Miyashiro, JM; Tao, Z; Woods, KW; Penning, TD; Souers, AJ Pyridine CDK9 kinase inhibitors US Patent US9650358 Publication Date 5/16/2017 | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Cyclin-dependent kinase 9 | |||
| Name: | Cyclin-dependent kinase 9 | ||
| Synonyms: | C-2K | CDC2L4 | CDK9 | CDK9_HUMAN | Cell division cycle 2-like protein kinase 4 | Cell division protein kinase 9 | Cyclin-Dependent Kinase 9 (CDK9) | Cyclin-dependent kinase 9 (CDK9) | Serine/threonine-protein kinase PITALRE | TAK | Tat-associated kinase complex catalytic subunit | ||
| Type: | Enzyme Subunit | ||
| Mol. Mass.: | 42789.13 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | n/a | ||
| Residue: | 372 | ||
| Sequence: |
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| BDBM307808 | |||
| n/a | |||
| Name | BDBM307808 | ||
| Synonyms: | BDBM307918 | BDBM307919 | N-{5-chloro-4-[1-(3-fluorobenzyl)-1H-benzimidazol-6-yl]pyridin-2-yl}-6-azaspiro[3.5]nonan-2-amine | US9650358, Example 104 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C27H27ClFN5 | ||
| Mol. Mass. | 475.988 | ||
| SMILES | Fc1cccc(Cn2cnc3ccc(cc23)-c2cc(NC3CC4(C3)CCCNC4)ncc2Cl)c1 |(2.76,10.77,;3.23,9.31,;4.74,8.99,;5.22,7.52,;4.19,6.38,;2.68,6.7,;1.65,5.55,;2.13,4.09,;1.22,2.84,;2.13,1.6,;3.59,2.07,;4.92,1.3,;6.26,2.07,;6.26,3.61,;4.92,4.38,;3.59,3.61,;7.59,4.38,;7.59,5.92,;8.92,6.69,;8.92,8.23,;10.26,9,;10.66,10.49,;12.14,10.09,;11.75,8.6,;13.48,9.32,;14.81,10.09,;14.81,11.63,;13.48,12.4,;12.14,11.63,;10.26,5.92,;10.26,4.38,;8.92,3.61,;8.92,2.07,;2.2,8.16,)| | ||
| Structure | 
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