http://www.cnr.it/ontology/cnr/individuo/prodotto/ID18750
First \"hybrid\" ligands of vanilloid TRPV1 and cannabinoid CB(2) receptors and non-polyunsaturated fatty acid-derived CB(2)-selective ligands. (Articolo in rivista)
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- First \"hybrid\" ligands of vanilloid TRPV1 and cannabinoid CB(2) receptors and non-polyunsaturated fatty acid-derived CB(2)-selective ligands. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.febslet.2005.12.069 (literal)
- Alternative label
Appendino G. , Cascio M.G. , Bacchiega S., Schiano Moriello A., Minassi A., Thomas A., Ross R., Pertwee R., De Petrocellis L., Di Marzo V. (2006)
First "hybrid" ligands of vanilloid TRPV1 and cannabinoid CB(2) receptors and non-polyunsaturated fatty acid-derived CB(2)-selective ligands.
in FEBS letters (Print); ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, AMSTERDAM (Paesi Bassi)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Appendino G. , Cascio M.G. , Bacchiega S., Schiano Moriello A., Minassi A., Thomas A., Ross R., Pertwee R., De Petrocellis L., Di Marzo V. (literal)
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- Dipartimento di Scienze Chimiche, Alimentari, Farmaceutiche e Farmacologiche, Via Bovio 6, 28100 Novara, Italy
b Endocannabinoid Research Group, Institute of Biomolecular Chemistry, CNR, Via Campi Flegrei 34, 80078 Pozzuoli, NA, Italy
c Department of Pharmaceutical Science, Università degli Studi di Salerno, via Ponte Don Melillo, 84084 Fisciano, SA, Italyd
e Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK (literal)
- Titolo
- First \"hybrid\" ligands of vanilloid TRPV1 and cannabinoid CB(2) receptors and non-polyunsaturated fatty acid-derived CB(2)-selective ligands. (literal)
- Abstract
- 12-Phenylacetyl-ricinoleoyl-vanillamide (phenylacetylrinvanil, PhAR, IDN5890), is an ultra-potent agonist of human vanilloid TRPV1 receptors also endowed with moderate affinity for human cannabinoid CB2 receptors. To improve its CB2 affinity and temper its potency at TRPV1, the modification of the polar headgroup and the lipophilic 12-acylgroup of PhAR was pursued. Replacement of the vanillyl headgroup of PhAR with various aromatic or alkyl amino groups decreased activity at TRPV1 receptors, although the dopamine, cyclopropylamine, 1?-(R)- and 1?-(S)-methyl-ethanolamine, and ethanolamine derivatives retained significant potency (EC50 31126nM). Within these compounds, the 12-phenylacetylricinoleyl cyclopropylamide and ethanolamide were the strongest ligands at CB2 receptors, with Ki of 22 and 44nM, and 14- and >20-fold selectivity over cannabinoid CB1 receptors, respectively. The propyl- and allyl-derivatives also exhibited high affinity at CB2 receptors (Ki=40 and 22nM, with 40 and >80-fold selectivity over CB1 receptors, respectively), but no activity at TRPV1 receptors. The cyclopropyl- and allyl-derivatives behaved as CB2 inverse agonists in the GTP-?-S binding assay. Addition of para-methoxy, -tert-butyl or -chlorine groups to the 12-phenylacetyl moiety of PhAR produced compounds that retained full potency at TRPV1 receptors, but with improved selectivity over CB2 or CB1 receptors. Thus, the manipulation of PhAR led to the development of the first CB2/TRPV1 dual ligands and of an entirely new class of inverse agonists at CB2 receptors. Both types of compounds might find application in the treatment of inflammation, and represent new molecular probes to investigate the endocannabinoidendovanilloid signalling system. (literal)
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