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pubmed-article:19144517pubmed:abstractTextWe identified a series of 4-hydroxyquinolines bearing a C1 to C15 alkyl chain at the C2 position and a carbethoxy/carboxy group at the C3 position of the quinoline nucleus (MC compounds), endowed with selective inhibitory activity against the p300/CBP HAT enzymes. Enzyme inhibition was investigated using in vitro HAT assays and by western blot analysis of cellular lysates to examine the acetylation levels of histone H3 and alpha-tubulin. When tested in U937 cells, some compounds displayed pro-apoptotic or cytodifferentiating properties.lld:pubmed
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pubmed-article:19144517pubmed:year2009lld:pubmed
pubmed-article:19144517pubmed:articleTitleIdentification of 4-hydroxyquinolines inhibitors of p300/CBP histone acetyltransferases.lld:pubmed
pubmed-article:19144517pubmed:affiliationIstituto Pasteur-Fondazione Cenci Bolognetti, Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza Università di Roma, P.le A. Moro 5, 00185 Roma, Italy. antonello.mai@uniroma1.itlld:pubmed
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