| Reaction Details |
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 | Report a problem with these data |
| Target | Serine/threonine-protein kinase pim-1 |
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| Ligand | BDBM192586 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1622453 (CHEMBL3864805) |
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| IC50 | 0.062000±n/a nM |
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| Citation |  Wurz, RP; Sastri, C; D'Amico, DC; Herberich, B; Jackson, CLM; Pettus, LH; Tasker, AS; Wu, B; Guerrero, N; Lipford, JR; Winston, JT; Yang, Y; Wang, P; Nguyen, Y; Andrews, KL; Huang, X; Lee, MR; Mohr, C; Zhang, JD; Reid, DL; Xu, Y; Zhou, Y; Wang, HL Discovery of imidazopyridazines as potent Pim-1/2 kinase inhibitors. Bioorg Med Chem Lett26:5580-5590 (2016) [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 |
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| 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) |
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| Type: | Protein |
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| Mol. Mass.: | 35681.82 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P11309 |
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| Residue: | 313 |
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| Sequence: | MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSD
NLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLIL
ERPEPVQDLFDFITERGALQEELARSFFWQVLEAVRHCHNCGVLHRDIKDENILIDLNRG
ELKLIDFGSGALLKDTVYTDFDGTRVYSPPEWIRYHRYHGRSAAVWSLGILLYDMVCGDI
PFEHDEEIIRGQVFFRQRVSSECQHLIRWCLALRPSDRPTFEEIQNHPWMQDVLLPQETA
EIHLHSLSPGPSK
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| BDBM192586 |
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| n/a |
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| Name | BDBM192586 |
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| Synonyms: | US9187486, 54 |
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| Type | Small organic molecule |
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| Emp. Form. | C23H23F2N7 |
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| Mol. Mass. | 435.4724 |
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| SMILES | C[C@@H]1[C@@H](N)CCCN1c1ccncc1Nc1ncc2ccc(nn12)-c1c(F)cccc1F |r| |
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| Structure | 
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