Reaction Details |
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Target | Aurora kinase A |
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Ligand | BDBM50446982 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1291250 (CHEMBL3117035) |
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IC50 | 58±n/a nM |
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Citation | Su, Q; Ioannidis, S; Chuaqui, C; Almeida, L; Alimzhanov, M; Bebernitz, G; Bell, K; Block, M; Howard, T; Huang, S; Huszar, D; Read, JA; Rivard Costa, C; Shi, J; Su, M; Ye, M; Zinda, M Discovery of 1-methyl-1H-imidazole derivatives as potent Jak2 inhibitors. J Med Chem57:144-58 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Aurora kinase A |
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Name: | Aurora kinase A |
Synonyms: | AIK | AIRK1 | ARK1 | AURA | AURKA | AURKA_HUMAN | AYK1 | Aurora 2 | Aurora kinase A (AURA) | Aurora kinase A (AURKA) | Aurora kinase A (Aurora A) | Aurora kinase A (Aurora-2) | Aurora-related kinase 1 | Aurora/IPL1-related kinase 1 | BTAK | Breast tumor-amplified kinase | Breast-tumor-amplified kinase | IAK1 | STK15 | STK6 | Serine/threonine kinase 15 | Serine/threonine-protein kinase 6 | Serine/threonine-protein kinase aurora A | aurora-2 | hARK1 |
Type: | Serine/threonine-protein kinase |
Mol. Mass.: | 45830.98 |
Organism: | Homo sapiens (Human) |
Description: | O14965 |
Residue: | 403 |
Sequence: | MDRSKENCISGPVKATAPVGGPKRVLVTQQFPCQNPLPVNSGQAQRVLCPSNSSQRVPLQ
AQKLVSSHKPVQNQKQKQLQATSVPHPVSRPLNNTQKSKQPLPSAPENNPEEELASKQKN
EESKKRQWALEDFEIGRPLGKGKFGNVYLAREKQSKFILALKVLFKAQLEKAGVEHQLRR
EVEIQSHLRHPNILRLYGYFHDATRVYLILEYAPLGTVYRELQKLSKFDEQRTATYITEL
ANALSYCHSKRVIHRDIKPENLLLGSAGELKIADFGWSVHAPSSRRTTLCGTLDYLPPEM
IEGRMHDEKVDLWSLGVLCYEFLVGKPPFEANTYQETYKRISRVEFTFPDFVTEGARDLI
SRLLKHNPSQRPMLREVLEHPWITANSSKPSNCQNKESASKQS
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BDBM50446982 |
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n/a |
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Name | BDBM50446982 |
Synonyms: | CHEMBL3116050 |
Type | Small organic molecule |
Emp. Form. | C16H16FN9 |
Mol. Mass. | 353.3569 |
SMILES | C[C@H](Nc1nc(Nc2cn(C)cn2)c2cc[nH]c2n1)c1ncc(F)cn1 |r| |
Structure |
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