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Title2-Amino-2,3-dihydro-1H-indene-5-carboxamide-Based Discoidin Domain Receptor 1 (DDR1) Inhibitors: Design, Synthesis, and in Vivo Antipancreatic Cancer Efficacy.
Journal, issue, pagesJ. Med. Chem., Vol. 62, Page 7431-7444, Year 2019
Publish dateSep 19, 2018 (structure data deposition date)
AuthorsZhu, D. / Huang, H. / Pinkas, D.M. / Luo, J. / Ganguly, D. / Fox, A.E. / Arner, E. / Xiang, Q. / Tu, Z.C. / Bullock, A.N. ...Zhu, D. / Huang, H. / Pinkas, D.M. / Luo, J. / Ganguly, D. / Fox, A.E. / Arner, E. / Xiang, Q. / Tu, Z.C. / Bullock, A.N. / Brekken, R.A. / Ding, K. / Lu, X.
External linksJ. Med. Chem. / PubMed:31310125
MethodsX-ray diffraction
Resolution1.96 Å
Structure data

PDB-6hp9:
Structure of the kinase domain of human DDR1 in complex with a 2-Amino-2,3-Dihydro-1H-Indene-5-Carboxamide-based inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.96 Å

Chemicals

ChemComp-GKB:
(2~{R})-~{N}-[3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)phenyl]-2-(pyrimidin-5-ylamino)-2,3-dihydro-1~{H}-indene-5-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / DDR1 / Structural Genomics / Structural Genomics Consortium / SGC

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