http://www.cnr.it/ontology/cnr/individuo/prodotto/ID237319
Analogues of perillaketone as highly potent agonists of TRPA1 channel (Articolo in rivista)
- Type
- Label
- Analogues of perillaketone as highly potent agonists of TRPA1 channel (Articolo in rivista) (literal)
- Anno
- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.foodchem.2013.05.063 (literal)
- Alternative label
Bassoli, A., Borgonovo, G., Morini, G., De Petrocellis, L., Schiano Moriello, A., Di Marzo, V. (2013)
Analogues of perillaketone as highly potent agonists of TRPA1 channel
in Food chemistry; elsevier B.V., Amsterdam (Paesi Bassi)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bassoli, A., Borgonovo, G., Morini, G., De Petrocellis, L., Schiano Moriello, A., Di Marzo, V. (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
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- Note
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- Department of Food, Environment and Nutritional Sciences, University of Milano, Via Celoria 2, Milano 20133, Italy
University of Gastronomic Sciences, Pollenzo (CN), Italy
Endocannabinoid Research Group, Institute of Cybernetics, ''Eduardo Caianiello'', CNR, Pozzuoli (NA), Italy
Endocannabinoid Research Group, Institute of Biomolecular Chemistry, CNR, Pozzuoli (NA), Italy (literal)
- Titolo
- Analogues of perillaketone as highly potent agonists of TRPA1 channel (literal)
- Abstract
- Transient receptor potential (TRP) channels represent interesting molecular target structures involved in
a number of different physiological and pathophysiological systems. In particular, TRPA1 channel is
involved in nociception and in sensory perception of many pungent chemesthetic compounds, which
are widespread in spices and food plants, including Perilla frutescens. A natural compound from P. frutescens
(isoegomaketone) and 16 synthetic derivatives of perillaketone have been prepared and tested
in vitro on rTRPA1 expressed in HEK293 cells and their potency, efficacy and desensibilisation activity
measured. Most derivatives proved to be high potency agonists of TRPA1, with a potency higher than
most natural agonists reported in the literature. These furylketones derivatives, represent a new class
of chemical structures active on TRPA1 with many potential applications in the agrifood and pharmaceutical
industry. (literal)
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