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TitleA Novel Potent Oral Series of VEGFR2 Inhibitors Abrogate Tumor Growth by Inhibiting Angiogenesis.
Journal, issue, pagesJ. Med. Chem., Vol. 59, Page 132-146, Year 2016
Publish dateNov 20, 2015 (structure data deposition date)
AuthorsBold, G. / Schnell, C. / Furet, P. / McSheehy, P. / Bruggen, J. / Mestan, J. / Manley, P.W. / Druckes, P. / Burglin, M. / Durler, U. ...Bold, G. / Schnell, C. / Furet, P. / McSheehy, P. / Bruggen, J. / Mestan, J. / Manley, P.W. / Druckes, P. / Burglin, M. / Durler, U. / Loretan, J. / Reuter, R. / Wartmann, M. / Theuer, A. / Bauer-Probst, B. / Martiny-Baron, G. / Allegrini, P. / Goepfert, A. / Wood, J. / Littlewood-Evans, A.
External linksJ. Med. Chem. / PubMed:26629594
MethodsX-ray diffraction
Resolution2.5 Å
Structure data

PDB-5ew3:
Human Vascular Endothelial Growth Factor Receptor 2 (KDR) Kinase Domain in complex with AAL993
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-5T2:
2-(pyridin-4-ylmethylamino)-~{N}-[3-(trifluoromethyl)phenyl]benzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / kdr / kinase domain / ATP-binding site / VEGFR2 inhibitors

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