beta-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol lipase.

نویسندگان

  • Marion Feledziak
  • Catherine Michaux
  • Allan Urbach
  • Geoffray Labar
  • Giulio G Muccioli
  • Didier M Lambert
  • Jacqueline Marchand-Brynaert
چکیده

A library of 30 beta-lactams has been prepared from (3R,4R)-3-[(R)-1'-(tbutyldimethylsilyloxy)-ethyl]-4-acetoxy-2-azetidinone, and the corresponding deacetoxy derivative, by sequential N- and O-functionalizations with various omega-alkenoyl and omega-arylalkanoyl chains. All compounds were selective inhibitors of hFAAH versus hMGL, and IC(50) values in the nanomolar range (5-14 nM) were recorded for the best representatives. From time-dependent preincubation and rapid dilution studies, and from docking analyses in a homology model of the target enzyme, a reversible mechanism of inhibition of hFAAH is proposed.

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عنوان ژورنال:
  • Journal of medicinal chemistry

دوره 52 22  شماره 

صفحات  -

تاریخ انتشار 2009