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TitleSynthesis, SAR study, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase (FAAH) inhibitors.
Journal, issue, pagesBioorg. Med. Chem., Vol. 21, Page 28-41, Year 2013
Publish dateSep 28, 2012 (structure data deposition date)
AuthorsKono, M. / Matsumoto, T. / Kawamura, T. / Nishimura, A. / Kiyota, Y. / Oki, H. / Miyazaki, J. / Igaki, S. / Behnke, C.A. / Shimojo, M. / Kori, M.
External linksBioorg. Med. Chem. / PubMed:23218778
MethodsX-ray diffraction
Resolution2.91 Å
Structure data

PDB-4hbp:
Crystal Structure of FAAH in complex with inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.91 Å

Chemicals

ChemComp-17J:
4-(3-phenyl-1,2,4-thiadiazol-5-yl)-N-(pyridin-3-yl)piperazine-1-carboxamide

ChemComp-HOH:
WATER

Source
  • rattus norvegicus (Norway rat)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Fatty Acid Amide Hydrolase / Amidase activity / HYDROLASE-HYDROLASE INHIBITOR complex

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