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Journal of Medicinal Chemistry|February 28, 2009
Synthesis and pharmacological characterization of beta2-adrenergic agonist enantiomers: zilpaterolChristopher Kern, Thorsten Meyer, Serge Droux, et al.Journal of Medicinal Chemistry|December 17, 2008
Synthesis and evaluation of benzothiazole-based analogues as novel, potent, and selective fatty acid amide hydrolase inhibitorsXueqing Wang, Katerina Sarris, Karen Kage, et al.Journal of Medicinal Chemistry|December 17, 2008
Design and synthesis of a cyclic double mutant peptide (cyclo(87-99)[A91,A96]MBP87-99) induces altered responses in mice after conjugation to mannan: implications in the immunotherapy of multiple sclerosisMaria Katsara, George Deraos, Theodore Tselios, et al.Journal of Medicinal Chemistry|December 17, 2008
Synthesis and biological evaluation of vinca alkaloids and phomopsin hybridsQuoc Anh Ngo, Fanny Roussi, Anthony Cormier, et al.Journal of Medicinal Chemistry|December 17, 2008
Discovery of a new class of potential multifunctional atypical antipsychotic agents targeting dopamine D3 and serotonin 5-HT1A and 5-HT2A receptors: design, synthesis, and effects on behaviorStefania Butini, Sandra Gemma, Giuseppe Campiani, et al.Journal of Medicinal Chemistry|March 24, 2009
Role of the hydrogen bonding heteroatom-Lys53 interaction between the p38alpha mitogen-activated protein (MAP) kinase and pyridinyl-substituted 5-membered heterocyclic ring inhibitorsBassam Abu Thaher, Pierre Koch, Verena Schattel, et al.Journal of Medicinal Chemistry|March 24, 2009
Design, synthesis, and evaluation of novel fluoroquinolone-aminoglycoside hybrid antibioticsVarvara Pokrovskaya, Valery Belakhov, Mariana Hainrichson, et al.Journal of Medicinal Chemistry|March 24, 2009
Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: a series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylasesSiavosh Mahboobi, Stefan Dove, Andreas Sellmer, et al.Journal of Medicinal Chemistry|March 25, 2009
Evaluation of antioxidant properties of monoaromatic derivatives of pulvinic acidsDamien Habrant, Stéphane Poigny, Muriel Ségur-Derai, et al.Journal of Medicinal Chemistry|March 25, 2009
Development of novel aminoglycoside (NB54) with reduced toxicity and enhanced suppression of disease-causing premature stop mutationsIgor Nudelman, Annie Rebibo-Sabbah, Marina Cherniavsky, et al.Pageof 3,141