15 articles for J Dubois
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
New indolizine-chalcones as potent inhibitors of human farnesyltransferase: Design, synthesis and biological evaluation.
Alexandru Ioan Cuza University
Studies on phenothiazines: New microtubule-interacting compounds with phenothiazine A-ring as potent antineoplastic agents.
Alexandru Ioan Cuza University
Highly improved antiparasitic activity after introduction of an N-benzylimidazole moiety on protein farnesyltransferase inhibitors.
Cnrs Upr2301
Novel indolizine derivatives with unprecedented inhibitory activity on human farnesyltransferase.
Alexandru Ioan Cuza University
Chemical and biological explorations of the electrophilic reactivity of the bioactive marine natural product halenaquinone with biomimetic nucleophiles.
University of Auckland
New bioactive halenaquinone derivatives from South Pacific marine sponges of the genus Xestospongia.
National Museum of Natural History
Design and Synthesis of Tubulin and Histone Deacetylase Inhibitor Based on iso-Combretastatin A-4.
Paris-Saclay University
Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds.
Alexandru Ioan Cuza University
Synthesis and biological evaluation of a new series of N-ylides as protein farnesyltransferase inhibitors.
'Al. I. Cuza' University of Iasi
Synthesis and biological evaluation of a new series of phenothiazine-containing protein farnesyltransferase inhibitors.
Al. I. Cuza University of Iasi
Synthesis and biological evaluation of new phenothiazine derivatives bearing a pyrazole unit as protein farnesyltransferase inhibitors.
'Al. I. Cuza' University of Iasi
New farnesyltransferase inhibitors in the phenothiazine series.
Al. I. Cuza University of Iasi
Towards the synthesis of bisubstrate inhibitors of protein farnesyltransferase: Synthesis and biological evaluation of new farnesylpyrophosphate analogues.
Centre De Recherche De Gif-Sur-Yvette
