| Literature DB >> 23083016 |
Shakiru O Alapafuja1, Spyros P Nikas, Indu T Bharathan, Vidyanand G Shukla, Mahmoud L Nasr, Anna L Bowman, Nikolai Zvonok, Jing Li, Xiaomeng Shi, John R Engen, Alexandros Makriyannis.
Abstract
Sulfonyl fluorides are known to inhibit esterases. Early work from our laboratory has identified hexadecyl sulfonylfluoride (AM374) as a potent in vitro and in vivo inhibitor of fatty acid amide hydrolase (FAAH). We now report on later generation sulfonyl fluoride analogs that exhibit potent and selective inhibition of FAAH. Using recombinant rat and human FAAH, we show that 5-(4-hydroxyphenyl)pentanesulfonyl fluoride (AM3506) has similar inhibitory activity for both the rat and the human enzyme, while rapid dilution assays and mass spectrometry analysis suggest that the compound is a covalent modifier for FAAH and inhibits its action in an irreversible manner. Our SAR results are highlighted by molecular docking of key analogs.Entities:
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Year: 2012 PMID: 23083016 PMCID: PMC3678964 DOI: 10.1021/jm301205j
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446