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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase 13 | ||
| Ligand | BDBM50420749 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_842608 (CHEMBL2092446) | ||
| IC50 | 6.7±n/a nM | ||
| Citation |  Aiguadé, J; Balagué, C; Carranco, I; Caturla, F; Domínguez, M; Eastwood, P; Esteve, C; González, J; Lumeras, W; Orellana, A; Preciado, S; Roca, R; Vidal, L; Vidal, B Novel triazolopyridylbenzamides as potent and selective p38a inhibitors. Bioorg Med Chem Lett22:3431-6 (2012) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Mitogen-activated protein kinase 13 | |||
| Name: | Mitogen-activated protein kinase 13 | ||
| Synonyms: | MAP kinase p38 delta | MAPK13 | MK13_HUMAN | Mitogen-activated protein kinase 13 | Mitogen-activated protein kinase 13 (MAPK13) | Mitogen-activated protein kinase p38 | Mitogen-activated protein kinase p38 delta | PRKM13 | SAPK4 | Stress-activated protein kinase 4 | p38 delta/gamma | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 42097.16 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | O15264 | ||
| Residue: | 365 | ||
| Sequence: |
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| BDBM50420749 | |||
| n/a | |||
| Name | BDBM50420749 | ||
| Synonyms: | CHEMBL2087743 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C20H19F3N4O | ||
| Mol. Mass. | 388.3863 | ||
| SMILES | CC(C)c1nnc2c(F)c(c(F)cn12)-c1cc(cc(F)c1C)C(=O)NC1CC1 |(6.05,-42.79,;6.78,-41.43,;8.32,-41.38,;5.97,-40.13,;4.44,-40.28,;3.82,-38.87,;4.97,-37.85,;4.97,-36.32,;3.64,-35.55,;6.31,-35.56,;7.64,-36.32,;8.98,-35.55,;7.63,-37.86,;6.3,-38.63,;6.32,-34.02,;7.65,-33.25,;7.65,-31.7,;6.31,-30.93,;4.98,-31.7,;3.65,-30.93,;4.98,-33.25,;3.65,-34.02,;8.98,-30.92,;8.97,-29.38,;10.31,-31.69,;11.65,-30.91,;13.18,-30.91,;12.41,-29.58,)| | ||
| Structure | 
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