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TitleN-benzylpiperidinol derivatives as novel USP7 inhibitors: Structure-activity relationships and X-ray crystallographic studies.
Journal, issue, pagesEur. J. Med. Chem., Vol. 199, Page 112279-112279, Year 2020
Publish dateFeb 26, 2020 (structure data deposition date)
AuthorsLi, M. / Liu, S. / Chen, H. / Zhou, X. / Zhou, J. / Zhou, S. / Yuan, H. / Xu, Q.L. / Liu, J. / Cheng, K. ...Li, M. / Liu, S. / Chen, H. / Zhou, X. / Zhou, J. / Zhou, S. / Yuan, H. / Xu, Q.L. / Liu, J. / Cheng, K. / Sun, H. / Wang, Y. / Chen, C. / Wen, X.
External linksEur. J. Med. Chem. / PubMed:32497973
MethodsX-ray diffraction
Resolution2.255 Å
Structure data

PDB-6m1k:
USP7 in complex with a novel inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.255 Å

Chemicals

ChemComp-EZF:
methyl 4-[[4-[[3-[4-(aminomethyl)phenyl]-2-methyl-7-oxidanylidene-pyrazolo[4,3-d]pyrimidin-6-yl]methyl]-4-oxidanyl-piperidin-1-yl]methyl]-3-chloranyl-benzoate

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Inhibitor / Complex / USP7 / HYDROLASE / HYDROLASE-HYDROLASE INHIBITOR complex

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