Reaction Details |
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Target | Cyclin-dependent kinase 2 |
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Ligand | BDBM24627 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_763157 (CHEMBL1819980) |
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IC50 | 185000±n/a nM |
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Citation | Bamborough, P; Brown, MJ; Christopher, JA; Chung, CW; Mellor, GW Selectivity of kinase inhibitor fragments. J Med Chem54:5131-43 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cyclin-dependent kinase 2 |
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Name: | Cyclin-dependent kinase 2 |
Synonyms: | CDK2 | CDK2-Kinase | CDK2_HUMAN | CDKN2 | Cell division protein kinase 2 | Cyclin-dependent kinase 2 (CDK2) | Protein cereblon/Cyclin-dependent kinase 2 | p33 protein kinase |
Type: | Enzyme Subunit |
Mol. Mass.: | 33938.17 |
Organism: | Homo sapiens (Human) |
Description: | P24941 |
Residue: | 298 |
Sequence: | MENFQKVEKIGEGTYGVVYKARNKLTGEVVALKKIRLDTETEGVPSTAIREISLLKELNH
PNIVKLLDVIHTENKLYLVFEFLHQDLKKFMDASALTGIPLPLIKSYLFQLLQGLAFCHS
HRVLHRDLKPQNLLINTEGAIKLADFGLARAFGVPVRTYTHEVVTLWYRAPEILLGCKYY
STAVDIWSLGCIFAEMVTRRALFPGDSEIDQLFRIFRTLGTPDEVVWPGVTSMPDYKPSF
PKWARQDFSKVVPPLDEDGRSLLSQMLHYDPNKRISAKAALAHPFFQDVTKPVPHLRL
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BDBM24627 |
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n/a |
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Name | BDBM24627 |
Synonyms: | 1H-indazole | Indazole, 5 | Indazole, 6 |
Type | Small organic molecule |
Emp. Form. | C7H6N2 |
Mol. Mass. | 118.1359 |
SMILES | c1n[nH]c2ccccc12 |
Structure |
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