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Journal of Medicinal Chemistry|October 17, 2003
Thienyl and phenyl alpha-halomethyl ketones: new inhibitors of glycogen synthase kinase (GSK-3beta) from a library of compound searchingSantiago Conde, Daniel I Pérez, Ana Martínez, et al.Journal of Medicinal Chemistry|October 17, 2003
Receptor-guided alignment-based comparative 3D-QSAR studies of benzylidene malonitrile tyrphostins as EGFR and HER-2 kinase inhibitorsShantaram Kamath, John K BuolamwiniJournal of Medicinal Chemistry|October 17, 2003
Structure-activity relationships of the p38alpha MAP kinase inhibitor 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)naph- thalen-1-yl]urea (BIRB 796)John Regan, Alison Capolino, Pier F Cirillo, et al.Journal of Medicinal Chemistry|October 17, 2003
Design and synthesis of 4-azaindoles as inhibitors of p38 MAP kinaseAlejandra Trejo, Humberto Arzeno, Michelle Browner, et al.Journal of Medicinal Chemistry|October 17, 2003
Potent inhibition of NTPase/helicase of the West Nile Virus by ring-expanded ("fat") nucleoside analoguesNing Zhang, Huan-Ming Chen, Verena Koch, et al.Journal of Medicinal Chemistry|October 31, 2003
Discovery of (aryloxopropenyl)pyrrolyl hydroxyamides as selective inhibitors of class IIa histone deacetylase homologue HD1-AAntonello Mai, Silvio Massa, Riccardo Pezzi, et al.Journal of Medicinal Chemistry|October 31, 2003
Dissociation of antibacterial and hemolytic activities of an amphipathic peptide antibioticChuanguang Qin, Xiaofen Zhong, Xianzhang Bu, et al.Journal of Medicinal Chemistry|October 31, 2003
Large dimeric ligands with favorable pharmacokinetic properties and peroxisome proliferator-activated receptor agonist activity in vitro and in vivoPer Sauerberg, Paul S Bury, John P Mogensen, et al.Journal of Medicinal Chemistry|October 31, 2003
Prazosin-related compounds. Effect of transforming the piperazinylquinazoline moiety into an aminomethyltetrahydroacridine system on the affinity for alpha1-adrenoreceptorsMichela Rosini, Alessandra Antonello, Andrea Cavalli, et al.Journal of Medicinal Chemistry|October 31, 2003
Structure-activity relationships of gamma-MSH analogues at the human melanocortin MC3, MC4, and MC5 receptors. Discovery of highly selective hMC3R, hMC4R, and hMC5R analoguesPreeti Balse-Srinivasan, Paolo Grieco, Minying Cai, et al.Pageof 3,141