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Methods in Molecular Biology (Clifton, N.J.)|September 30, 2022
Alternative Ligands at Melatonin ReceptorsCéline Legros, Said Yous, Jean A BoutinJournal of Enzyme Inhibition and Medicinal Chemistry|August 22, 2006
Homology modelling of the serotoninergic 5-HT2c receptorAmaury Farce, Sebastien Dilly, Said Yous, et al.Journal of Biochemical and Biophysical Methods|July 5, 2005
Preparative HPLC separation of methoxytetralins, ligands for melatonin receptors, containing two chiral centers with polysaccharide chiral stationary phases. Determination of enantiomeric purityEmmanuelle Lipka, Abdelhalim Guelzim, Said Yous, et al.Cancer Chemotherapy and Pharmacology|January 14, 2011
Interactions of bexarotene (LGD1069, Targretin) with the coagulation systemAnne Hespel, Najet Mejdoubi-Charef, Said Yous, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|November 27, 2007
Quantitative structure-activity relationships studies of antioxidant hexahydropyridoindoles and flavonoid derivativesAnne-Catherine Durand, Amaury Farce, Pascal Carato, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|September 29, 2004
Synthesis and evaluation of benzoxazolinonic imidazoles and derivatives as non-steroidal aromatase inhibitorsCeline Nativelle-Serpentini, Safa Moslemi, Said Yous, et al.The Journal of Pharmacology and Experimental Therapeutics|October 28, 2021
A putative new melatonin binding site in sheep brain, MTx: preliminary observations and characteristicsPreety Shabajee-Alibay, Anne Bonnaud, Benoit Malpaux, et al.Medchemcomm|December 19, 2017
Bitopic fluorescent antagonists of the A2A adenosine receptor based on pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine functionalized congenersRomain Duroux, Antonella Ciancetta, Philip Mannes, et al.European Journal of Medicinal Chemistry|October 30, 2015
Design and synthesis of fused tetrahydroisoquinoline-iminoimidazolinesValeria Moas-Héloire, Nicolas Renault, Vania Batalha, et al.European Journal of Biochemistry|January 14, 2004
New substrate analogues of human serotonin N-acetyltransferase produce in situ specific and potent inhibitorsGilles Ferry, Caroline Ubeaud, Julien Mozo, et al.Pageof 1