| Reaction Details |
|---|
 | Report a problem with these data |
| Target | Serine/threonine-protein kinase pim-1 |
|---|
| Ligand | BDBM50434652 |
|---|
| Substrate/Competitor | n/a |
|---|
| Meas. Tech. | ChEMBL_960801 (CHEMBL2388109) |
|---|
| Ki | 1.1±n/a nM |
|---|
| 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 |
|---|
| More Info.: | Get all data from this article, Assay Method |
|---|
| |
| Serine/threonine-protein kinase pim-1 |
|---|
| 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
|
|
|
|---|
| BDBM50434652 |
|---|
| n/a |
|---|
| Name | BDBM50434652 |
|---|
| Synonyms: | CHEMBL2387467 |
|---|
| Type | Small organic molecule |
|---|
| Emp. Form. | C21H14FN5O2 |
|---|
| Mol. Mass. | 387.3666 |
|---|
| SMILES | Fc1ccc(NC(=O)c2c[nH]n3c2nc(Cc2ccc(cc2)C#N)cc3=O)cc1 |
|---|
| Structure | 
|
|---|
Search and Browse
