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TitleDiscovery of Novel Benzimidazoles as Potent Inhibitors of TIE-2 and VEGFR-2 Tyrosine Kinase Receptors.
Journal, issue, pagesJ. Med. Chem., Vol. 50, Page 4453-4470, Year 2007
Publish dateJan 9, 2007 (structure data deposition date)
AuthorsHasegawa, M. / Nishigaki, N. / Washio, Y. / Kano, K. / Harris, P.A. / Sato, H. / Mori, I. / West, R.I. / Shibahara, M. / Toyoda, H. ...Hasegawa, M. / Nishigaki, N. / Washio, Y. / Kano, K. / Harris, P.A. / Sato, H. / Mori, I. / West, R.I. / Shibahara, M. / Toyoda, H. / Wang, L. / Nolte, R.T. / Veal, J.M. / Cheung, M.
External linksJ. Med. Chem. / PubMed:17676829
MethodsX-ray diffraction
Resolution2.05 Å
Structure data

PDB-2oh4:
Crystal structure of Vegfr2 with a benzimidazole-urea inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-GIG:
METHYL (5-{4-[({[2-FLUORO-5-(TRIFLUOROMETHYL)PHENYL]AMINO}CARBONYL)AMINO]PHENOXY}-1H-BENZIMIDAZOL-2-YL)CARBAMATE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Vascular endothelial growth factor receptor 2 / Tyrosine-protein kinase / Angiogenesis / ATP-binding / Phosphorylation / Kinase insert domain receptor / Protein-tyrosine kinase receptor Flk-1

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