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Structure paper

TitleDiscovery of amido-benzisoxazoles as potent c-Kit inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 5115-5117, Year 2008
Publish dateJul 16, 2008 (structure data deposition date)
AuthorsKunz, R.K. / Rumfelt, S. / Chen, N. / Zhang, D. / Tasker, A.S. / Burli, R. / Hungate, R. / Yu, V. / Nguyen, Y. / Whittington, D.A. ...Kunz, R.K. / Rumfelt, S. / Chen, N. / Zhang, D. / Tasker, A.S. / Burli, R. / Hungate, R. / Yu, V. / Nguyen, Y. / Whittington, D.A. / Meagher, K.L. / Plant, M. / Tudor, Y. / Schrag, M. / Xu, Y. / Ng, G.Y. / Hu, E.
External linksBioorg. Med. Chem. Lett. / PubMed:18723346
MethodsX-ray diffraction
Resolution2.9 Å
Structure data

PDB-3dtw:
Crystal structure of the VEGFR2 kinase domain in complex with a benzisoxazole inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.9 Å

Chemicals

ChemComp-A96:
6-chloro-N-pyrimidin-5-yl-3-{[3-(trifluoromethyl)phenyl]amino}-1,2-benzisoxazole-7-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / angiogenesis / receptor tyrosine kinase

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