Reaction Details |
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Target | Cyclin-dependent kinase 6 |
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Ligand | BDBM556330 |
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Substrate/Competitor | n/a |
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Meas. Tech. | CDK6 Inhibition Assay |
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IC50 | 2.90±n/a nM |
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Citation | Song, Y; Chen, X Substituted pyrimidines as CDK4/6 inhibitors US Patent US11351170 Publication Date 6/7/2022 |
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More Info.: | Get all data from this article, Assay Method |
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Cyclin-dependent kinase 6 |
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Name: | Cyclin-dependent kinase 6 |
Synonyms: | CDK6 | CDK6_HUMAN | CDKN6 | Cell division protein kinase 6 | Cyclin-dependent kinase 6 (CDK 6) | Serine/threonine-protein kinase PLSTIRE |
Type: | Enzyme Subunit |
Mol. Mass.: | 36937.42 |
Organism: | Homo sapiens (Human) |
Description: | Q00534 |
Residue: | 326 |
Sequence: | MEKDGLCRADQQYECVAEIGEGAYGKVFKARDLKNGGRFVALKRVRVQTGEEGMPLSTIR
EVAVLRHLETFEHPNVVRLFDVCTVSRTDRETKLTLVFEHVDQDLTTYLDKVPEPGVPTE
TIKDMMFQLLRGLDFLHSHRVVHRDLKPQNILVTSSGQIKLADFGLARIYSFQMALTSVV
VTLWYRAPEVLLQSSYATPVDLWSVGCIFAEMFRRKPLFRGSSDVDQLGKILDVIGLPGE
EDWPRDVALPRQAFHSKSAQPIEKFVTDIDELGKDLLLKCLTFNPAKRISAYSALSHPYF
QDLERCKENLDSHLPPSQNTSELNTA
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BDBM556330 |
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n/a |
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Name | BDBM556330 |
Synonyms: | N-(5-((1-ethylpiperidin-4-yl)methoxy)pyridin-2-yl)-5-fluoro-4-(5-fluoro-1,1-dimethyl-2,3-dihydro-1H-benzo[d]pyrrolo[1,2-a]imidazol-7-yl)pyridin-2-amine (Compound 60) | US11351170, Example 9 |
Type | Small organic molecule |
Emp. Form. | C30H34F2N6O |
Mol. Mass. | 532.6274 |
SMILES | CCN1CCC(COc2ccc(Nc3cc(c(F)cn3)-c3cc(F)c4nc5CCC(C)(C)n5c4c3)nc2)CC1 |
Structure |
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