Please use this identifier to cite or link to this item: http://elea.unisa.it/xmlui/handle/10556/2229
Title: Design and synthesis of modulators of apoptotic activity
Authors: Di Sarno, Veronica
Sbardella, Gianluca
Campiglia, Pietro
Keywords: P53;MDM2;SM13
Issue Date: 23-Mar-2016
Publisher: Universita degli studi di Salerno
Abstract: p53 is a transcription factor with tumour suppressor properties, which is able to induce mitochondrial apoptosis independently of its transcriptional activity. Analogues of the spiro[imidazo[1,5-c] thiazole-3,3′-indoline] -2′,5,7(6H,7aH) -trione, previously synthesized from my research group, as p53 modulators were synthesized during my PhD, aiming to explore new structural requirements at the thiazolidine domain to increase the antiproliferative activity and improve p53 modulation. Derivative 5-bromo-3′- (cyclohexane carbonyl) -1-methyl-2oxospiro[indoline-3,2′-thiazolidine] (SM13) emerged as the most potent compound of all series, inhibiting, in vitro, 30% of p53−MDM2 interaction at 5 μM and the cell growth of different human tumor cells at nanomolar concentrations... [edited by author]
Description: 2014 - 2015
URI: http://hdl.handle.net/10556/2229
Appears in Collections:Scienze farmaceutiche

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