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Bioorganic & Medicinal Chemistry|August 25, 2009
Synthesis, structure-affinity relationships, and modeling of AMDA analogs at 5-HT2A and H1 receptors: structural factors contributing to selectivityJitesh R Shah, Philip D Mosier, Bryan L Roth, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2012
Discovery of diphenyl lactam derivatives as N-type calcium channel blockersGeorge A Doherty, Pramila Bhatia, Timothy A Vortherms, et al.
Journal of Medicinal Chemistry|August 18, 2006
Binding of sulfonyl-containing arylalkylamines at human 5-HT6 serotonin receptorsDonald Sikazwe, Mikhail L Bondarev, Małgorzata Dukat, et al.
ACS Chemical Neuroscience|January 15, 2015
The first structure-activity relationship studies for designer receptors exclusively activated by designer drugsXin Chen, Hyunah Choo, Xi-Ping Huang, et al.
The Journal of Physiology|September 18, 2013
Modulation of the autonomic nervous system and behaviour by acute glial cell Gq protein-coupled receptor activation in vivoCendra Agulhon, Kristen M Boyt, Alison Xiaoqiao Xie, et al.
Journal of the American Chemical Society|May 26, 2011
Design, synthesis, and validation of a β-turn mimetic library targeting protein-protein and peptide-receptor interactionsLandon R Whitby, Yoshio Ando, Vincent Setola, et al.
Bioorganic & Medicinal Chemistry Letters|August 10, 2010
N-tetrahydrothiochromenoisoxazole-1-carboxamides as selective antagonists of cloned human 5-HT2BYoon Jin Kwon, Simon Saubern, James M Macdonald, et al.
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