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TitleStructure-Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5-b]Pyridin-2-one-Based p38 MAP Kinase Inhibitors: Part 2.
Journal, issue, pagesChemmedchem, Vol. 14, Page 2093-2101, Year 2019
Publish dateApr 5, 2019 (structure data deposition date)
AuthorsKaieda, A. / Takahashi, M. / Fukuda, H. / Okamoto, R. / Morimoto, S. / Gotoh, M. / Miyazaki, T. / Hori, Y. / Unno, S. / Kawamoto, T. ...Kaieda, A. / Takahashi, M. / Fukuda, H. / Okamoto, R. / Morimoto, S. / Gotoh, M. / Miyazaki, T. / Hori, Y. / Unno, S. / Kawamoto, T. / Tanaka, T. / Itono, S. / Takagi, T. / Sugimoto, H. / Okada, K. / Lane, W. / Sang, B.C. / Saikatendu, K. / Matsunaga, S. / Miwatashi, S.
External linksChemmedchem / PubMed:31697454
MethodsX-ray diffraction
Resolution2.5 Å
Structure data

PDB-6ohd:
P38 in complex with T-3220137
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-MKP:
3-(3-tert-butyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-6-yl)-4-methyl-N-(1,2-oxazol-3-yl)benzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/INHIBITOR / SBDD / P38 / kinase / PROTEIN BINDING / TRANSFERASE-INHIBITOR complex

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