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dc.contributor.authorRoche, Michelle
dc.contributor.authorFinn, David P.
dc.date.accessioned2014-01-07T15:30:49Z
dc.date.available2014-01-07T15:30:49Z
dc.date.issued2009
dc.identifier.citationRoche, M., Finn, D., Enna, S. J., & Bylund, D. B. (2009). 6-Iodonordihydrocapsaicin xPharm: The Comprehensive Pharmacology Reference (pp. 1-4). New York: Elsevier.en_US
dc.identifier.isbn978-0-08-055232-3
dc.identifier.urihttp://hdl.handle.net/10379/3943
dc.descriptionBook section (reference)en_US
dc.description.abstract6-Iodonordihydrocapsaicin was first synthesized by Giovanni Appendino at the Department of Chemical, Food, Pharmaceutical and Pharmacological Sciences (DiSCAFF), Novara, Italy, while developing a series of halogenated derivatives of capsaicin (Appendino et al., 2003). This compound is a potent antagonist at the vanilloid VR-1 (TRPV1) receptor in several in vitro preparations. Its activity in vivo has not been examined. Recent evidence indicates that 6-iodonordihydrocapsaicin may also antagonize transient receptor potential channels of melastatin type 8 (TRPM8) (De Petrocellis et al., 2007)en_US
dc.formatapplication/docen_US
dc.language.isoenen_US
dc.relation.ispartofXpharmen
dc.subject6-Iodonordihydrocapsaicinen_US
dc.subjectPhysiologyen_US
dc.subjectChemistryen_US
dc.title6-iodonordihydrocapsaicinen_US
dc.typeBook chapteren_US
dc.date.updated2013-07-09T15:04:51Z
dc.identifier.doi10.1016/B978-008055232-3.64025-5
dc.local.publishedsourcehttp://dx.doi.org/10.1016/B978-008055232-3.64025-5en_US
dc.description.peer-reviewedpeer-reviewed
dc.contributor.funder|~|
dc.internal.rssid4603109
dc.local.contactMichelle Roche, Dept Of Physiology, Nui Galway. 5427 Email: michelle.roche@nuigalway.ie
dc.local.copyrightcheckedNo
dc.local.versionACCEPTED
nui.item.downloads213


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