Reaction Details |
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Target | Cyclin-dependent kinase 1 |
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Ligand | BDBM50164720 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_304675 (CHEMBL827874) |
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IC50 | 135±n/a nM |
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Citation | Verma, S; Nagarathnam, D; Shao, J; Zhang, L; Zhao, J; Wang, Y; Li, T; Mull, E; Enyedy, I; Wang, C; Zhu, Q; Altieri, M; Jordan, J; Dang, TT; Reddy, S Substituted aminobenzimidazole pyrimidines as cyclin-dependent kinase inhibitors. Bioorg Med Chem Lett15:1973-7 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cyclin-dependent kinase 1 |
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Name: | Cyclin-dependent kinase 1 |
Synonyms: | CDC2 | CDC28A | CDK1 | CDK1_HUMAN | CDKN1 | Cell division control protein 2 homolog | Cell division protein kinase 1 | Cyclin-dependent kinase 1 (CDK1) | P34CDC2 | p34 protein kinase |
Type: | Enzyme Subunit |
Mol. Mass.: | 34101.08 |
Organism: | Homo sapiens (Human) |
Description: | P06493 |
Residue: | 297 |
Sequence: | MEDYTKIEKIGEGTYGVVYKGRHKTTGQVVAMKKIRLESEEEGVPSTAIREISLLKELRH
PNIVSLQDVLMQDSRLYLIFEFLSMDLKKYLDSIPPGQYMDSSLVKSYLYQILQGIVFCH
SRRVLHRDLKPQNLLIDDKGTIKLADFGLARAFGIPIRVYTHEVVTLWYRSPEVLLGSAR
YSTPVDIWSIGTIFAELATKKPLFHGDSEIDQLFRIFRALGTPNNEVWPEVESLQDYKNT
FPKWKPGSLASHVKNLDENGLDLLSKMLIYDPAKRISGKMALNHPYFNDLDNQIKKM
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BDBM50164720 |
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n/a |
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Name | BDBM50164720 |
Synonyms: | (3H-Benzoimidazol-5-yl)-(4-o-tolylsulfanyl-5-trifluoromethyl-pyrimidin-2-yl)-amine | CHEMBL194124 |
Type | Small organic molecule |
Emp. Form. | C19H14F3N5S |
Mol. Mass. | 401.408 |
SMILES | Cc1ccccc1Sc1nc(Nc2ccc3nc[nH]c3c2)ncc1C(F)(F)F |
Structure |
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