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The Journal of Infectious Diseases|November 1, 1995
Weak binding of VX-478 to human plasma proteins and implications for anti-human immunodeficiency virus therapyD J Livington, S Pazhanisamy, D J Porter, et al.Journal of Pharmaceutical Sciences|July 2, 1998
Metabolism of amprenavir in liver microsomes: role of CYP3A4 inhibition for drug interactionsC J Decker, L M Laitinen, G W Bridson, et al.Journal of Immunology (Baltimore, Md. : 1950)|March 15, 1993
Immunosuppressive activity of [MeBm2t]1-, D-diaminobutyryl-8-, and D-diaminopropyl-8-cyclosporin analogues correlates with inhibition of calcineurin phosphatase activityP A Nelson, Y Akselband, A Kawamura, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2000
Novel inhibitors of HIV protease: design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffoldsA Spaltenstein, M R Almond, W J Bock, et al.Journal of Medicinal Chemistry|October 16, 1992
Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural productP D Williams, M G Bock, R D Tung, et al.The Journal of Pharmacology and Experimental Therapeutics|January 1, 1991
In vitro pharmacological profile of a novel structural class of oxytocin antagonistsD J Pettibone, B V Clineschmidt, E V Lis, et al.Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Design, synthesis, and conformational analysis of a novel series of HIV protease inhibitorsC T Baker, F G Salituro, J J Court, et al.Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Design and synthesis of novel conformationally restricted HIV protease inhibitorsF G Salituro, C T Baker, J J Court, et al.Acta Crystallographica. Section D, Biological Crystallography|July 1, 1995
Design, synthesis and structure of non-macrocyclic inhibitors of FKBP12, the major binding protein for the immunosuppressant FK506D M Armistead, M C Badia, D D Deininger, et al.Pageof 1