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European Journal of Medicinal Chemistry|December 22, 2014
Rapid synthesis of 4-arylchromenes from ortho-substituted alkynols: A versatile access to restricted isocombretastatin A-4 analogues as antitumor agentsDolor Renko, Olivier Provot, Evelia Rasolofonjatovo, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 25, 2014
Overlapping binding sites drive allosteric agonism and positive cooperativity in type 4 metabotropic glutamate receptorsXavier Rovira, Fanny Malhaire, Pauline Scholler, et al.
European Journal of Medicinal Chemistry|March 28, 2012
Conformationnally restricted naphthalene derivatives type isocombretastatin A-4 and isoerianin analogues: synthesis, cytotoxicity and antitubulin activityEvelia Rasolofonjatovo, Olivier Provot, Abdallah Hamze, et al.
European Journal of Medicinal Chemistry|July 31, 2016
Synthesis, biological evaluation and molecular modeling studies of imidazo[1,2-a]pyridines derivatives as protein kinase inhibitorsMarie Lawson, Jordi Rodrigo, Blandine Baratte, et al.
European Journal of Medicinal Chemistry|January 29, 2013
Design, synthesis and anticancer properties of 5-arylbenzoxepins as conformationally restricted isocombretastatin A-4 analogsEvelia Rasolofonjatovo, Olivier Provot, Abdallah Hamze, et al.
Chemmedchem|March 2, 2011
Discovery of isoerianin analogues as promising anticancer agentsSamir Messaoudi, Abdallah Hamze, Olivier Provot, et al.
Chemmedchem|October 13, 2011
B-ring-modified isocombretastatin A-4 analogues endowed with interesting anticancer activitiesAbdallah Hamze, Evelia Rasolofonjatovo, Olivier Provot, et al.
European Journal of Medicinal Chemistry|November 5, 2013
α- and β-hydrazino acid-based pseudopeptides inhibit the chymotrypsin-like activity of the eukaryotic 20S proteasomeAndrea Bordessa, Massaba Keita, Xavier Maréchal, et al.
British Journal of Pharmacology|November 20, 2009
Phe369(7.38) at human 5-HT(7) receptors confers interspecies selectivity to antagonists and partial agonistsThibault Varin, Hugo Gutiérrez-de-Terán, Marián Castro, et al.
Journal of Medicinal Chemistry|July 18, 2012
Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerizationLaure Dufau, Ana Sofia Marques Ressurreição, Roberto Fanelli, et al.
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