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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Mitogen-activated protein kinase 13 | ||
| Ligand | BDBM50420752 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_842608 (CHEMBL2092446) | ||
| IC50 | 12±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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| BDBM50420752 | |||
| n/a | |||
| Name | BDBM50420752 | ||
| Synonyms: | CHEMBL2087746 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C20H20F3N5O | ||
| Mol. Mass. | 403.4009 | ||
| SMILES | Cc1c(F)cc(cc1-c1c(F)cn2c(nnc2c1F)C(C)(C)N)C(=O)NC1CC1 |(3.97,.97,;5.3,1.74,;5.3,3.28,;3.97,4.05,;6.63,4.05,;7.97,3.29,;7.97,1.74,;6.63,.97,;6.63,-.57,;7.96,-1.33,;9.29,-.56,;7.95,-2.88,;6.62,-3.65,;6.29,-5.15,;4.76,-5.3,;4.14,-3.89,;5.29,-2.87,;5.29,-1.34,;3.96,-.56,;7.09,-6.45,;6.37,-7.8,;8.63,-6.4,;7.86,-7.77,;9.3,4.06,;9.29,5.6,;10.63,3.3,;11.96,4.07,;13.5,4.07,;12.73,5.4,)| | ||
| Structure | 
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