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TitleDesign, synthesis, and evaluation of 5-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine derivatives: novel VEGFR2 kinase inhibitors binding to inactive kinase conformation.
Journal, issue, pagesBioorg. Med. Chem., Vol. 18, Page 7260-7273, Year 2010
Publish dateAug 24, 2011 (structure data deposition date)
AuthorsOguro, Y. / Miyamoto, N. / Okada, K. / Takagi, T. / Iwata, H. / Awazu, Y. / Miki, H. / Hori, A. / Kamiyama, K. / Imamura, S.
External linksBioorg. Med. Chem. / PubMed:20833055
MethodsX-ray diffraction
Resolution1.55 Å
Structure data

PDB-3vhe:
Crystal structure of human VEGFR2 kinase domain with a novel pyrrolopyrimidine inhibitor.
Method: X-RAY DIFFRACTION / Resolution: 1.55 Å

Chemicals

ChemComp-42Q:
1-{2-fluoro-4-[(5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yl)oxy]phenyl}-3-[3-(trifluoromethyl)phenyl]urea

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / KINASE DOMAIN / KINASE / TRANSFERASE-TRANSFERASE INHIBITOR complex

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