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Journal of Medicinal Chemistry|January 23, 2004
Structural analysis and optimization of NK(1) receptor antagonists through modulation of atropisomer interconversion propertiesJeffrey S Albert, Cyrus Ohnmacht, Peter R Bernstein, et al.Journal of Medicinal Chemistry|January 23, 2004
Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognitionAlexander Weber, Angela Casini, Andreas Heine, et al.Journal of Medicinal Chemistry|January 23, 2004
SAR studies of dihydro-beta-agarofuran sesquiterpenes as inhibitors of the multidrug-resistance phenotype in a Leishmania tropica line overexpressing a P-glycoprotein-like transporterFernando Cortés-Selva, Mercedes Campillo, Carolina P Reyes, et al.Journal of Medicinal Chemistry|January 23, 2004
Synthesis and biological evaluation of 2,3,5-substituted [1,2,4]thiadiazoles as allosteric modulators of adenosine receptorsAdrianus M C H van den Nieuwendijk, Daniele Pietra, Laura Heitman, et al.Journal of Medicinal Chemistry|January 23, 2004
Design, synthesis, and biological evaluation of thio-containing compounds with serum HDL-cholesterol-elevating propertiesHassan Elokdah, Theodore S Sulkowski, Magid Abou-Gharbia, et al.Journal of Medicinal Chemistry|December 30, 2003
Design, synthesis, molecular modeling studies, and calpain inhibitory activity of novel alpha-ketoamides incorporating polar residues at the P1'-positionIsaac O Donkor, Jie Han, Xiaozhang ZhengJournal of Medicinal Chemistry|December 30, 2003
Synthesis and structure-activity relationships of 5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine derivatives: novel arginine vasopressin antagonistsHidetsura Cho, Kengo Murakami, Hiroyuki Nakanishi, et al.Journal of Medicinal Chemistry|December 30, 2003
Potent inhibitors of the Plasmodium falciparum enzymes plasmepsin I and II devoid of cathepsin D inhibitory activityKarolina Ersmark, Isabella Feierberg, Sinisa Bjelic, et al.Journal of Medicinal Chemistry|December 30, 2003
NMR structural characterization of peptide inhibitors bound to the Hepatitis C virus NS3 protease: design of a new P2 substituentNathalie Goudreau, Dale R Cameron, Pierre Bonneau, et al.Journal of Medicinal Chemistry|December 30, 2003
Synthesis, in vitro evaluation, and antileishmanial activity of water-soluble prodrugs of buparvaquoneAntti Mäntylä, Tracy Garnier, Jarkko Rautio, et al.Pageof 3,137