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Bioorganic & Medicinal Chemistry Letters|November 30, 2005
Designing rapid onset selective serotonin re-uptake inhibitors. Part 1: Structure-activity relationships of substituted (1S,4S)-4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydro-1-naphthaleneamineDonald S Middleton, Mark Andrews, Paul Glossop, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2008
Designing rapid onset selective serotonin re-uptake inhibitors. 2: structure-activity relationships of substituted (aryl)benzylaminesDonald S Middleton, Mark Andrews, Paul Glossop, et al.Experimental and Clinical Psychopharmacology|October 4, 2016
Initial feasibility and validity of a prospective memory training program in a substance use treatment populationMary M Sweeney, Olga Rass, Patrick S Johnson, et al.Bioorganic & Medicinal Chemistry Letters|September 3, 2011
Discovery of PF-184563, a potent and selective V1a antagonist for the treatment of dysmenorrhoea. The influence of compound flexibility on microsomal stabilityPatrick S Johnson, Thomas Ryckmans, Justin Bryans, et al.Journal of Medicinal Chemistry|January 18, 2014
Design of potent and selective inhibitors to overcome clinical anaplastic lymphoma kinase mutations resistant to crizotinibQinhua Huang, Ted W Johnson, Simon Bailey, et al.Pageof 5