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Journal of Separation Science|April 28, 2007
HPLC retention behavior on hydride-based stationary phasesJoseph J Pesek, Maria T Matyska, Susan LarrabeeBMC Medical Education|September 2, 2022
A student-led interprofessional virtual outreach program for people with HIV during the Covid-19 pandemic: a pilot program at an academic medical center in BostonDaniel A Solomon, Susan Larrabee, Joshua Ellis, et al.Drug Development and Industrial Pharmacy|July 10, 2008
Physicochemical properties of the nucleoside prodrug R1626 leading to high oral bioavailabilityMichael Brandl, Xiaoyang Wu, Marites Holper, et al.Bioorganic & Medicinal Chemistry Letters|August 28, 2009
Non-nucleoside inhibitors of HCV polymerase NS5B. Part 4: structure-based design, synthesis, and biological evaluation of benzo[d]isothiazole-1,1-dioxidesJavier de Vicente, Robert T Hendricks, David B Smith, et al.Journal of Medicinal Chemistry|March 3, 2006
Discovery of S-[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2,3-dihydroxypropoxy)phenyl]methanone (RO3201195), an orally bioavailable and highly selective inhibitor of p38 MAP kinaseDavid M Goldstein, Tom Alfredson, Jay Bertrand, et al.Bioorganic & Medicinal Chemistry Letters|May 22, 2009
Non-nucleoside inhibitors of HCV polymerase NS5B. Part 2: Synthesis and structure-activity relationships of benzothiazine-substituted quinolinedionesJavier de Vicente, Robert T Hendricks, David B Smith, et al.Pageof 1