Reaction Details | |||
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Target | Mitogen-activated protein kinase 13 | ||
Ligand | BDBM50420750 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_842608 (CHEMBL2092446) | ||
IC50 | 10±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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BDBM50420750 | |||
n/a | |||
Name | BDBM50420750 | ||
Synonyms: | CHEMBL2087744 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H17F3N4O | ||
Mol. Mass. | 386.3704 | ||
SMILES | Cc1c(F)cc(cc1-c1c(F)cn2c(nnc2c1F)C1CC1)C(=O)NC1CC1 |(17.06,-33.61,;18.39,-32.84,;18.39,-31.3,;17.06,-30.53,;19.72,-30.53,;21.06,-31.29,;21.06,-32.84,;19.73,-33.62,;19.73,-35.16,;21.05,-35.92,;22.39,-35.15,;21.04,-37.46,;19.71,-38.23,;19.38,-39.73,;17.85,-39.88,;17.23,-38.47,;18.38,-37.45,;18.38,-35.92,;17.05,-35.14,;20.19,-41.03,;20.24,-42.56,;21.54,-41.75,;22.39,-30.52,;22.38,-28.98,;23.73,-31.28,;25.06,-30.51,;26.59,-30.51,;25.82,-29.18,)| | ||
Structure |