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pubmed-article:12443769pubmed:abstractTextFour new analogues of Targretin where the carboxylic acid function was replaced by an N,N-dimethyl-S-aryl carbamate or N,N-dimethyl-O-arylthiocarbamate function, were synthesized. Compounds 5, 6 and 7 have shown to be more potent than the parent compound to induce apoptosis of HL-60 cells.lld:pubmed
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pubmed-article:12443769pubmed:authorpubmed-author:BaghdiguianSt...lld:pubmed
pubmed-article:12443769pubmed:authorpubmed-author:CommesThérèse...lld:pubmed
pubmed-article:12443769pubmed:authorpubmed-author:MonteroJean-L...lld:pubmed
pubmed-article:12443769pubmed:authorpubmed-author:WinumJean-Yve...lld:pubmed
pubmed-article:12443769pubmed:authorpubmed-author:LeydetAlainAlld:pubmed
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pubmed-article:12443769pubmed:pagination3529-32lld:pubmed
pubmed-article:12443769pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:12443769pubmed:articleTitleSynthesis of new Targretin analogues that induce apoptosis in leukemia HL-60 cells.lld:pubmed
pubmed-article:12443769pubmed:affiliationLaboratoire de Chimie Biomoléculaire, UMR 5032, Université Montpellier II - CNRS - Laboratoires Mayoly Spindler, ENSCM, 8 Rue de l'Ecole Normale, 34296 Montpellier Cedex, France.lld:pubmed
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