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TitleThe Design, Synthesis, and Biological Evaluation of Potent Receptor Tyrosine Kinase Inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 22, Page 4979-, Year 2012
Publish dateMay 31, 2012 (structure data deposition date)
AuthorsKim, M.H. / Tsuhako, A.L. / Co, E.W. / Aftab, D.T. / Bentzien, F. / Chen, J. / Cheng, W. / Engst, S. / Goon, L. / Klein, R.R. ...Kim, M.H. / Tsuhako, A.L. / Co, E.W. / Aftab, D.T. / Bentzien, F. / Chen, J. / Cheng, W. / Engst, S. / Goon, L. / Klein, R.R. / Le, D.T. / Mac, M. / Parks, J.J. / Qian, F. / Rodriquez, M. / Stout, T.J. / Till, J.H. / Won, K.A. / Wu, X. / Michael Yakes, F. / Yu, P. / Zhang, W. / Zhao, Y. / Lamb, P. / Nuss, J.M. / Xu, W.
External linksBioorg. Med. Chem. Lett. / PubMed:22765894
MethodsX-ray diffraction
Resolution2.33 Å
Structure data

PDB-4aw5:
Complex of the EphB4 kinase domain with an oxindole inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.33 Å

Chemicals

ChemComp-30K:
(3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(5-methoxy-1H-benzimidazol-2-yl)(phenyl)methylidene]-1,3-dihydro-2H-indol-2-one

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE

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