Synthesis and Quantitative Structure−Activity Relationship of Fatty Acid Amide Hydrolase Inhibitors: Modulation at the N-Portion of Biphenyl-3-yl Alkylcarbamates
Author(s) -
Marco Mor,
Alessio Lodola,
Silvia Rivara,
Federica Vacondio,
Andrea Duranti,
Andrea Tontini,
Silvano Sanchini,
Giovanni Piersanti,
Jason R. Clapper,
Alvin R. King,
Giorgio Tarzia,
Daniele Piomelli
Publication year - 2008
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/jm801482q
Subject(s) - chemistry , biphenyl , amide , stereochemistry , structure–activity relationship , fatty acid amide hydrolase , fatty acid , hydrolase , enzyme , biochemistry , organic chemistry , in vitro , receptor , antagonist , cannabinoid receptor
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