Synthesis and pharmacological activity of a potent inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerol. (Articolo in rivista)

Type
Label
  • Synthesis and pharmacological activity of a potent inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerol. (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/cmdc.200800442 (literal)
Alternative label
  • Tiziana Bisogno; James J. Burston; Ravi Rai; Marco Allarà; Bijali Saha; Anu Mahadevan; Raj K. Razdan; Jenny L. Wiley; Vincenzo Di Marzo (2009)
    Synthesis and pharmacological activity of a potent inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerol.
    in ChemMedChem (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Tiziana Bisogno; James J. Burston; Ravi Rai; Marco Allarà; Bijali Saha; Anu Mahadevan; Raj K. Razdan; Jenny L. Wiley; Vincenzo Di Marzo (literal)
Pagina inizio
  • 946 (literal)
Pagina fine
  • 950 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 4 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 6 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Endocannabinoid Research Group, Institute of Biomolecular Chemistry, Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, Comprensorio Olivetti, Pozzuoli (NA) (Italy), Fax.: (+39) 081-8041770 Department of Pharmacology and Toxicology, Virginia Commonwealth University, 410 North 12th St., Rm 746, P.O. Box 980613, Richmond, VA 23298 (USA) Organix Inc., 240 Salem St., Woburn, MA 01801 (USA) (literal)
Titolo
  • Synthesis and pharmacological activity of a potent inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerol. (literal)
Abstract
  • Biosynthesis Inhibition: O-5596, a new inhibitor of the biosynthesis of the endocannabinoid, 2-arachidonoylglycerol, was synthesized and found to be potent (IC50=100 nM) and selective versus other proteins and enzymes of the endocannabinoid system in vitro and active in vivo at reducing food intake in mice. (literal)
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