Reaction Details | |||
---|---|---|---|
Report a problem with these data | |||
Target | Mitogen-activated protein kinase 11 | ||
Ligand | BDBM50122922 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_124648 (CHEMBL731909) | ||
IC50 | 64±n/a nM | ||
Citation | Colletti, SL; Frie, JL; Dixon, EC; Singh, SB; Choi, BK; Scapin, G; Fitzgerald, CE; Kumar, S; Nichols, EA; O'Keefe, SJ; O'Neill, EA; Porter, G; Samuel, K; Schmatz, DM; Schwartz, CD; Shoop, WL; Thompson, CM; Thompson, JE; Wang, R; Woods, A; Zaller, DM; Doherty, JB Hybrid-designed inhibitors of p38 MAP kinase utilizing N-arylpyridazinones. J Med Chem46:349-52 (2003) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Mitogen-activated protein kinase 11 | |||
Name: | Mitogen-activated protein kinase 11 | ||
Synonyms: | MAP Kinase p38 beta | MK11_MOUSE | Mapk11 | Mitogen-activated protein kinase 11 | Mitogen-activated protein kinase p38 beta | Prkm11 | p38B | ||
Type: | Enzyme | ||
Mol. Mass.: | 41390.66 | ||
Organism: | Mus musculus (mouse) | ||
Description: | Q9WUI1 | ||
Residue: | 364 | ||
Sequence: |
| ||
BDBM50122922 | |||
n/a | |||
Name | BDBM50122922 | ||
Synonyms: | 6-[2-(2-Chloro-4-fluoro-phenyl)-imidazo[1,2-a]pyridin-3-yl]-2-(2,6-dichloro-phenyl)-2H-pyridazin-3-one | CHEMBL118768 | ||
Type | Small organic molecule | ||
Emp. Form. | C23H12Cl3FN4O | ||
Mol. Mass. | 485.725 | ||
SMILES | Fc1ccc(-c2nc3ccccn3c2-c2ccc(=O)n(n2)-c2c(Cl)cccc2Cl)c(Cl)c1 |(2.33,-8.2,;3.67,-7.43,;3.51,-5.89,;4.77,-5,;6.17,-5.63,;7.4,-4.74,;8.87,-5.23,;9.78,-3.99,;11.32,-3.83,;11.95,-2.43,;11.04,-1.17,;9.52,-1.34,;8.89,-2.73,;7.42,-3.2,;6.1,-2.41,;4.76,-3.18,;3.43,-2.41,;3.44,-.87,;2.11,-.1,;4.77,-.12,;6.1,-.87,;4.77,1.42,;6.1,2.19,;7.44,1.42,;6.1,3.75,;4.77,4.52,;3.44,3.73,;3.44,2.19,;2.1,1.42,;6.32,-7.16,;7.73,-7.79,;5.09,-8.06,)| | ||
Structure |