Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism (Articolo in rivista)

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Label
  • Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism (Articolo in rivista) (literal)
Anno
  • 2008-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/jm800978m (literal)
Alternative label
  • Giorgio Ortar; Tiziana Bisogno; Alessia Ligresti; Enrico Morera; Marianna Nalli; Vincenzo Di Marzo. (2008)
    Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism
    in Journal of medicinal chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Giorgio Ortar; Tiziana Bisogno; Alessia Ligresti; Enrico Morera; Marianna Nalli; Vincenzo Di Marzo. (literal)
Pagina inizio
  • 6970 (literal)
Pagina fine
  • 6979 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://pubs.acs.org/doi/pdf/10.1021/jm800978m (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 51 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 21 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza UniVersita` di Roma, piazzale Aldo Moro 5, 00185 Roma, Italy, Endocannabinoid Research Group, Institute of Biomolecular Chemistry, Consiglio Nazionale delle Ricerche, Via dei Campi Flegrei 34, 80078 Pozzuoli (Napoli), Italy (literal)
Titolo
  • Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism (literal)
Abstract
  • A series of 21 analogues of tetrahydrolipstatin (THL, 1) were synthesized and tested as inhibitors of the formation or hydrolysis of the endocannabinoid 2-arachidonoylglycerol (2-AG). Three of the novel compounds, i.e., 11, 13, and 15, inhibited 2-AG formation via the diacylglycerol lipase R (DAGLR) with IC50 values lower than 50 nM (IC50 of THL ) 1 µM) and were between 23- and 375-fold selective vs 2-AG hydrolysis by monoacylglycerol lipase (MAGL) as well as vs cannabinoid CB1 and CB2 receptors and anandamide hydrolysis by fatty acid amide hydrolase (FAAH). Three other THL analogues, i.e., 14, 16, and 18, were slightly more potent than THL against DAGLR and appreciably selective vs MAGL, CB receptors, and FAAH (15-26-fold). One compound, i.e., 8, was a potent inhibitor of MAGL-like activity (IC50 ) 0.41 µM), and relatively (~7-fold) selective vs the other targets tested. (literal)
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