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Bioorganic & Medicinal Chemistry|March 29, 2008
Design and synthesis of benzofuranic derivatives as new ligands at the melatonin-binding site MT3Mohamed Ettaoussi, Basile Péres, Fréderique Klupsch, et al.
Bioorganic & Medicinal Chemistry|January 15, 2014
New melatonin (MT1/MT2) ligands: design and synthesis of (8,9-dihydro-7H-furo[3,2-f]chromen-1-yl) derivativesElodie Landagaray, Mohamed Ettaoussi, Véronique Leclerc, et al.
European Journal of Medicinal Chemistry|December 4, 2012
Synthesis, antiproliferative activity and tubulin targeting effect of acridinone and dioxophenothiazine derivativesValérie Verones, Nathalie Flouquet, Marie Lecoeur, et al.
Bioorganic & Medicinal Chemistry|September 10, 2008
Synthesis of 3-phenylnaphthalenic derivatives as new selective MT(2) melatoninergic ligandsSophie Poissonnier-Durieux, Mohamed Ettaoussi, Basile Pérès, et al.
European Journal of Medicinal Chemistry|May 21, 2018
Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitorsBruno Oyallon, Marie Brachet-Botineau, Cédric Logé, et al.
Bioorganic & Medicinal Chemistry|March 31, 2009
Design and synthesis of 3-phenyltetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands. Part IISophie Durieux, Angéline Chanu, Christophe Bochu, et al.
European Journal of Medicinal Chemistry|June 14, 2017
Anti-diabetic activity of fused PPARγ-SIRT1 ligands with limited body-weight gain by mimicking calorie restriction and decreasing SGK1 expressionCeline Pirat, Catherine Dacquet, Veronique Leclerc, et al.
Bioorganic & Medicinal Chemistry|May 7, 2010
Design, synthesis and pharmacological evaluation of novel naphthalenic derivatives as selective MT(1) melatoninergic ligandsChristophe Mésangeau, Basile Pérès, Carole Descamps-François, et al.
Chemmedchem|October 11, 2012
Effect of oxime ether incorporation in acyl indole derivatives on PPAR subtype selectivityMorgan Le Naour, Veronique Leclerc, Amaury Farce, et al.
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