Investigations on the 4-quinolone-3-carboxylic acid motif. 4. Identification of new potent and selective ligands for the cannabinoid type 2 receptor with diverse substitution patterns and antihyperalgesic effects in mice.
J Med Chem. 2011 Aug 11; 54(15):5444-53.JM

Abstract

Experimental evidence suggests that selective CB2 receptor modulators may provide access to antihyperalgesic agents devoid of psychotropic effects. Taking advantage of previous findings on structure-activity/selectivity relationships for a class of 4-quinolone-3-carboxamides, further structural modifications of the heterocyclic scaffold were explored, leading to the discovery of the 8-methoxy derivative 4a endowed with the highest affinity and selectivity ever reported for a CB2 ligand. The compound, evaluated in vivo in the formalin test, behaved as an inverse agonist by reducing at a dose of 6 mg/kg the second phase of the formalin-induced nocifensive response in mice.

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Authors+Show Affiliations

Pasquini S
Dipartimento Farmaco Chimico Tecnologico, Università degli Studi di Siena, Siena, Italy.
De Rosa M
No affiliation info available
Pedani V
No affiliation info available
Mugnaini C
No affiliation info available
Guida F
No affiliation info available
Luongo L
No affiliation info available
De Chiaro M
No affiliation info available
Maione S
No affiliation info available
Dragoni S
No affiliation info available
Frosini M
No affiliation info available
Ligresti A
No affiliation info available
Di Marzo V
No affiliation info available
Corelli F
No affiliation info available

MeSH

4-QuinolonesAdamantaneAnalgesicsAnimalsCell SurvivalHep G2 CellsHumansLigandsMiceQuinolonesRatsReceptor, Cannabinoid, CB2

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21702498