Reaction Details |
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Target | Serine/threonine-protein kinase pim-1 |
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Ligand | BDBM50434666 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_960801 (CHEMBL2388109) |
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Ki | 0.009000±n/a nM |
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Citation | Wang, X; Magnuson, S; Pastor, R; Fan, E; Hu, H; Tsui, V; Deng, W; Murray, J; Steffek, M; Wallweber, H; Moffat, J; Drummond, J; Chan, G; Harstad, E; Ebens, AJ Discovery of novel pyrazolo[1,5-a]pyrimidines as potent pan-Pim inhibitors by structure- and property-based drug design. Bioorg Med Chem Lett23:3149-53 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Serine/threonine-protein kinase pim-1 |
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Name: | Serine/threonine-protein kinase pim-1 |
Synonyms: | PIM-1 Kinase | PIM1 | PIM1_HUMAN | Proto-oncogene serine/threonine-protein kinase Pim-1 | Serine/threonine-protein kinase (PIM1) | Serine/threonine-protein kinase PIM | Serine/threonine-protein kinase PIM1 | Serine/threonine-protein kinase pim-1 (PIM1) |
Type: | Protein |
Mol. Mass.: | 35681.82 |
Organism: | Homo sapiens (Human) |
Description: | P11309 |
Residue: | 313 |
Sequence: | MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSD
NLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLIL
ERPEPVQDLFDFITERGALQEELARSFFWQVLEAVRHCHNCGVLHRDIKDENILIDLNRG
ELKLIDFGSGALLKDTVYTDFDGTRVYSPPEWIRYHRYHGRSAAVWSLGILLYDMVCGDI
PFEHDEEIIRGQVFFRQRVSSECQHLIRWCLALRPSDRPTFEEIQNHPWMQDVLLPQETA
EIHLHSLSPGPSK
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BDBM50434666 |
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n/a |
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Name | BDBM50434666 |
Synonyms: | CHEMBL2387471 |
Type | Small organic molecule |
Emp. Form. | C26H24F2N8O |
Mol. Mass. | 502.5186 |
SMILES | Fc1cccc(F)c1-c1cnc2[nH]cc(NC(=O)c3cnn4ccc(NCC5CCNCC5)nc34)c2c1 |
Structure |
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