Source:http://linkedlifedata.com/resource/pubmed/id/19144517
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2009-2-16
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pubmed:abstractText |
We 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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1464-3405
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1132-5
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pubmed:meshHeading |
pubmed-meshheading:19144517-Combinatorial Chemistry Techniques,
pubmed-meshheading:19144517-Histone Acetyltransferases,
pubmed-meshheading:19144517-Humans,
pubmed-meshheading:19144517-Hydroxyquinolines,
pubmed-meshheading:19144517-Molecular Structure,
pubmed-meshheading:19144517-Structure-Activity Relationship,
pubmed-meshheading:19144517-p300-CBP Transcription Factors
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pubmed:year |
2009
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pubmed:articleTitle |
Identification of 4-hydroxyquinolines inhibitors of p300/CBP histone acetyltransferases.
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pubmed:affiliation |
Istituto 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.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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