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European Journal of Medicinal Chemistry|March 25, 2000
University education of medicinal chemists: comparison of eight countriesC R Ganellin, L A Mitscher, B Clement, et al.Journal of Medicinal Chemistry|August 25, 2001
2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonistsG Spadoni, C Balsamini, G Diamantini, et al.Journal of Medicinal Chemistry|September 28, 1998
Melatonin receptor ligands: synthesis of new melatonin derivatives and comprehensive comparative molecular field analysis (CoMFA) studyM Mor, S Rivara, C Silva, et al.Bioorganic & Medicinal Chemistry|May 17, 2001
Synthesis, pharmacological characterization and QSAR studies on 2-substituted indole melatonin receptor ligandsM Mor, G Spadoni, B Di Giacomo, et al.Journal of Medicinal Chemistry|June 20, 1997
Conformationally restrained melatonin analogues: synthesis, binding affinity for the melatonin receptor, evaluation of the biological activity, and molecular modeling studyG Spadoni, C Balsamini, G Diamantini, et al.Journal of Medicinal Chemistry|September 11, 1998
2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonistsG Spadoni, C Balsamini, A Bedini, et al.Proceedings of the National Academy of Sciences of the United States of America|December 15, 2005
Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysisG Gobbi, F R Bambico, R Mangieri, et al.Journal of Medicinal Chemistry|October 6, 2000
Synthesis and SAR of new 5-phenyl-3-ureido-1,5-benzodiazepines as cholecystokinin-B receptor antagonistsA Ursini, A M Capelli, R A Carr, et al.Pageof 6