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Journal of Medicinal Chemistry|May 26, 2006
Novel antitrypanosomal agents based on palladium nitrofurylthiosemicarbazone complexes: DNA and redox metabolism as potential therapeutic targetsLucía Otero, Marisol Vieites, Lucía Boiani, et al.Journal of Medicinal Chemistry|May 26, 2006
Structure-activity relationships of new 1H-imidazo[4,5-c]quinolin-4-amine derivatives as allosteric enhancers of the A3 adenosine receptorAnikó Göblyös, Zhan-Guo Gao, Johannes Brussee, et al.Journal of Medicinal Chemistry|May 26, 2006
Discovery of a novel, orally active, small molecule gonadotropin-releasing hormone (GnRH) receptor antagonistHaitao Li, Kenna L Anderes, Eugenia A Kraynov, et al.Journal of Medicinal Chemistry|May 26, 2006
5-(Dimethoxymethyl)-2'-deoxyuridine: a novel gem diether nucleoside with anti-orthopoxvirus activityXuesen Fan, Xinying Zhang, Longhu Zhou, et al.Journal of Medicinal Chemistry|May 26, 2006
Discovery of huperzine A-tacrine hybrids as potent inhibitors of human cholinesterases targeting their midgorge recognition sitesSandra Gemma, Emanuele Gabellieri, Paul Huleatt, et al.Journal of Medicinal Chemistry|February 1, 1991
Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1 ,6] naphthyridines at alpha-adrenoceptorsR D Clark, D B Repke, J Berger, et al.Journal of Medicinal Chemistry|February 1, 1991
Conformationally defined neurotransmitter analogues. Selective inhibition of glutamate uptake by one pyrrolidine-2,4-dicarboxylate diastereomerR J Bridges, M S Stanley, M W Anderson, et al.Journal of Medicinal Chemistry|July 11, 2006
Iron binding dendrimers: a novel approach for the treatment of haemochromatosisTao Zhou, Hendrik Neubert, Ding Yong Liu, et al.Journal of Medicinal Chemistry|July 11, 2006
Docking and three-dimensional quantitative structure-activity relationship (3D QSAR) analyses of nonsteroidal progesterone receptor ligandsAnnu A Söderholm, Pekka T Lehtovuori, Tommi H NyrönenJournal of Medicinal Chemistry|July 11, 2006
C-(4,5,6-trimethoxyindan-1-yl)methanamine: a mescaline analogue designed using a homology model of the 5-HT2A receptorThomas H McLean, James J Chambers, Jason C Parrish, et al.Pageof 3,134