Mostrar el registro sencillo del ítem

dc.contributor.authorCruz López, Olga
dc.contributor.authorDiaz de Ceiro, Elixabet
dc.contributor.authorRubio Ruiz, Belén 
dc.contributor.authorEspejo Román, José Manuel 
dc.contributor.authorPeñalver, Pablo
dc.contributor.authorMorales Vega, Juan Carlos 
dc.contributor.authorCaboni, Maria Fiorenza
dc.contributor.authorConejo García, Ana 
dc.contributor.authorVerardo, Vito 
dc.date.accessioned2024-05-28T11:33:55Z
dc.date.available2024-05-28T11:33:55Z
dc.date.issued2024
dc.identifier.urihttps://hdl.handle.net/10481/92161
dc.description.abstractPolyunsaturated fatty acids and phenolic compounds are two families of natural products that have been widely investigated for their health benefits. The aim of this study was to prepare the novel phenolipid hydroxytyrosyl punicate (HT-PA) and evaluate its antiproliferative and antiparasitic properties. HT-PA was synthesized from hydroxytyrosol (HT) and punicic acid (PA) in a two-step chemical synthesis. HT-PA had an EC50 of 8.93 µM against non–small cell lung carcinoma A549 cells and was more active than HT or PA. It achieved a selectivity index of 11.20 for tumor cell line A549 over non-tumor cell line MCR-5. HT-PA displayed 80-fold and 60-fold greater activity against Trypanosoma brucei parasites (EC50 of 0.95 µM) compared with HT and PA, respectively, and > 100-fold selectivity for T. brucei over healthy MRC-5 cells.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleHydroxytyrosyl punicate: A first overview of a novel phenolipid with antiproliferative and antitrypanosomal activityes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.jff.2024.106249


Ficheros en el ítem

[PDF]

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 Internacional