Design, synthesis and biological evaluation of novel β-substituted indol-3-yl ethylamido melatoninergic analogues

dc.contributor.author	Βαρβαρέσου, Αθανασία	el
dc.contributor.author	Ιακώβου, Κρίτων	el
dc.contributor.author	Κουρουνάκη, Αγγελική Π.	el
dc.contributor.author	Stead, K.	en
dc.contributor.author	Sugden, David	el
dc.date.accessioned	2015-04-29T16:16:03Z
dc.date.available	2015-04-29T16:16:03Z
dc.date.issued	2015-04-29
dc.identifier.uri	http://hdl.handle.net/11400/9273
dc.rights	Αναφορά Δημιουργού-Μη Εμπορική Χρήση-Όχι Παράγωγα Έργα 3.0 Ηνωμένες Πολιτείες	*
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/3.0/us/	*
dc.source	http://onlinelibrary.wiley.com	en
dc.source	http://onlinelibrary.wiley.com/doi/10.1211/0022357021771869/abstract	en
dc.subject	Καλλυντικά
dc.subject	Χημικά παρασκευάσματα
dc.subject	Cosmetics
dc.subject	Chemical preparations
dc.title	Design, synthesis and biological evaluation of novel β-substituted indol-3-yl ethylamido melatoninergic analogues	en
heal.type	journalArticle
heal.classification	Aesthetics
heal.classification	Chemistry
heal.classification	Αισθητική
heal.classification	Χημεία
heal.classificationURI	http://id.loc.gov/authorities/subjects/sh85001441
heal.classificationURI	http://id.loc.gov/authorities/subjects/sh85022986
heal.classificationURI	N/A-Αισθητική
heal.classificationURI	N/A-Χημεία
heal.contributorName	Τσοτίνης, Ανδρέας	el
heal.identifier.secondary	10.1211/0022357021771869
heal.language	en
heal.access	campus
heal.recordProvider	Τεχνολογικό Εκπαιδευτικό Ίδρυμα Αθηνών. Σχολή Επαγγελμάτων Υγείας και Πρόνοιας. Τμήμα Αισθητικής και Κοσμητολογίας	el
heal.publicationDate	2010-02-18
heal.bibliographicCitation	Iakovou, K., Varvaresou, A., Kourounaki, Α.P., Stead, K., Sugden, D. et al. (2002) Design, synthesis and biological evaluation of novel β-substituted indol-3-yl ethylamido melatoninergic analogues. "Journal of Pharmacy and Pharmacology" 54 (1), p.147-156	en
heal.abstract	A series of new melatonin analogues have been synthesized. Interestingly, two of the new compounds, 11c and 11e, which did not show any appreciable affinity for the melatonin receptor, were found to be potent inhibitors of lipid peroxidation in rat liver microsomes. Analogue 11c, in particular, is a better antioxidant than melatonin.	en
heal.publisher	Wiley	en
heal.journalName	Journal of Pharmacy and Pharmacology	en
heal.journalType	peer-reviewed
heal.fullTextAvailability	false