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Journal of Medicinal Chemistry|April 1, 1977
Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase BR Nishizawa, T Saino, T Takita, et al.Journal of Medicinal Chemistry|April 1, 1977
Mercapto heterocyclic carboxylic acids, analogues of 3-mercaptopicolinic acidB Blank, N W DiTullio, F F Owings, et al.Journal of Medicinal Chemistry|April 1, 1977
Quinazolines as inhibitors of dihydrofolate reductase. 4. Classical analogues of folic and isofolic acidsJ B Hynes, D E Eason, C M Garrett, et al.Journal of Medicinal Chemistry|June 25, 1993
Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp-Phe sequence of fibrinogen. A proposal on the nature of the binding interaction between the Arg-guanidine of RGDX mimetics and the platelet GP IIb-IIIa receptorJ A Zablocki, M Miyano, R B Garland, et al.Journal of Medicinal Chemistry|June 25, 1993
Hypoxia-selective antitumor agents. 7. Metal complexes of aliphatic mustards as a new class of hypoxia-selective cytotoxins. Synthesis and evaluation of cobalt(III) complexes of bidentate mustardsD C Ware, B D Palmer, W R Wilson, et al.Journal of Medicinal Chemistry|June 25, 1993
Structure-based design of inhibitors of purine nucleoside phosphorylase. 2. 9-Alicyclic and 9-heteroalicyclic derivatives of 9-deazaguanineJ A Secrist, S Niwas, J D Rose, et al.Journal of Medicinal Chemistry|June 25, 1993
Inhibition and inactivation of presynaptic cholinergic markers using redox-reactive choline analogsP J Patel, W S Messer, R A HudsonJournal of Medicinal Chemistry|May 1, 1977
Synthesis and anti-herpes simplex activity of analogues of phosphonoacetic acidT R Herrin, J S Fairgrieve, R R Bower, et al.Journal of Medicinal Chemistry|May 1, 1977
5,6,7,8-Tetrahydroquinolines. 5. Antiulcer and antisecretory activity of 5,6,7,8-tetrahydroquinolinethioureas and related heterocyclesD E Beattie, R Crossley, A C Curran, et al.Journal of Medicinal Chemistry|December 8, 1995
(3SR,4aRS,6SR,8aRS)-6-(1H-tetrazol-5-yl)decahydroisoquinoline-3-carboxylic acid, a novel, competitive, systemically active NMDA and AMPA receptor antagonistP L Ornstein, M B Arnold, N K Allen, et al.Pageof 3,141