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European Journal of Medicinal Chemistry|August 1, 2008
N-acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues: synthesis and antiproliferative activitySara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.Bioorganic & Medicinal Chemistry|April 28, 2009
6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxisSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.European Journal of Medicinal Chemistry|October 29, 2008
Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitorsAndrea Spallarossa, Sara Cesarini, Angelo Ranise, et al.Bioorganic & Medicinal Chemistry|May 27, 2008
Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitorsSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.European Journal of Medicinal Chemistry|December 9, 2008
Parallel synthesis, molecular modelling and further structure-activity relationship studies of new acylthiocarbamates as potent non-nucleoside HIV-1 reverse transcriptase inhibitorsAndrea Spallarossa, Sara Cesarini, Angelo Ranise, et al.Journal of Medicinal Chemistry|March 12, 2010
A virtual screening hit reveals new possibilities for developing group III metabotropic glutamate receptor agonistsChelliah Selvam, Nadia Oueslati, Isabelle A Lemasson, et al.Journal of Medicinal Chemistry|May 27, 2005
Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivativesAngelo Ranise, Andrea Spallarossa, Sara Cesarini, et al.Journal of Medicinal Chemistry|February 6, 2018
Increased Potency and Selectivity for Group III Metabotropic Glutamate Receptor Agonists Binding at Dual sitesChelliah Selvam, Isabelle A Lemasson, Isabelle Brabet, et al.Pageof 2