Reaction Details |
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Target | Cyclin-dependent kinase 1 |
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Ligand | BDBM50214095 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_513579 (CHEMBL967075) |
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IC50 | 0.7±n/a nM |
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Citation | Bharate, SB; Mahajan, TR; Gole, YR; Nambiar, M; Matan, TT; Kulkarni-Almeida, A; Balachandran, S; Junjappa, H; Balakrishnan, A; Vishwakarma, RA Synthesis and evaluation of pyrazolo[3,4-b]pyridines and its structural analogues as TNF-alpha and IL-6 inhibitors. Bioorg Med Chem16:7167-76 (2008) [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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BDBM50214095 |
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n/a |
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Name | BDBM50214095 |
Synonyms: | CHEMBL248713 | CHEMBL511394 | N-((5-(3-(5-fluoro-1H-benzo[d]imidazol-2-yl)-1H-pyrazolo[3,4-b]pyridin-5-yl)pyridin-3-yl)methyl)ethanamine |
Type | Small organic molecule |
Emp. Form. | C21H18FN7 |
Mol. Mass. | 387.4129 |
SMILES | CCNCc1cncc(c1)-c1cnc2n[nH]c(-c3nc4ccc(F)cc4[nH]3)c2c1 |
Structure |
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