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Structure paper

TitleStructure-based design, synthesis, and evaluation of imidazo[1,2-b]pyridazine and imidazo[1,2-a]pyridine derivatives as novel dual c-Met and VEGFR2 kinase inhibitors.
Journal, issue, pagesBioorg. Med. Chem., Vol. 21, Page 7686-7698, Year 2013
Publish dateAug 8, 2012 (structure data deposition date)
AuthorsMatsumoto, S. / Miyamoto, N. / Hirayama, T. / Oki, H. / Okada, K. / Tawada, M. / Iwata, H. / Nakamura, K. / Yamasaki, S. / Miki, H. ...Matsumoto, S. / Miyamoto, N. / Hirayama, T. / Oki, H. / Okada, K. / Tawada, M. / Iwata, H. / Nakamura, K. / Yamasaki, S. / Miki, H. / Hori, A. / Imamura, S.
External linksBioorg. Med. Chem. / PubMed:24216091
MethodsX-ray diffraction
Resolution2.1 Å
Structure data

PDB-3vw8:
Crystal structure of human c-Met kinase domain with its inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-DF6:
N-({4-[(6,7-dimethoxyquinolin-4-yl)oxy]phenyl}carbamothioyl)-2-phenylacetamide

ChemComp-CL:
Unknown entry

ChemComp-HOH:
WATER

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

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