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5HO6

CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH CMPD.

Summary for 5HO6
Entry DOI10.2210/pdb5ho6/pdb
DescriptorHepatocyte growth factor receptor, 1-(6-{[6-(4-fluorophenyl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulfanyl}-1,3-benzothiazol-2-yl)-3-[2-(morpholin-4-yl)ethyl]urea (3 entities in total)
Functional Keywordstransferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight35857.53
Authors
Vallee, F.,Houtmann, J. (deposition date: 2016-01-19, release date: 2016-11-23, Last modification date: 2019-10-16)
Primary citationUgolini, A.,Kenigsberg, M.,Rak, A.,Vallee, F.,Houtmann, J.,Lowinski, M.,Capdevila, C.,Khider, J.,Albert, E.,Martinet, N.,Nemecek, C.,Grapinet, S.,Bacque, E.,Roesner, M.,Delaisi, C.,Calvet, L.,Bonche, F.,Semiond, D.,Egile, C.,Goulaouic, H.,Schio, L.
Discovery and Pharmacokinetic and Pharmacological Properties of the Potent and Selective MET Kinase Inhibitor 1-{6-[6-(4-Fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-ylsulfanyl]benzothiazol-2-yl}-3-(2-morpholin-4-ylethyl)urea (SAR125844).
J.Med.Chem., 59:7066-7074, 2016
Cited by
PubMed: 27355974
DOI: 10.1021/acs.jmedchem.6b00280
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.97 Å)
Structure validation

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