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Journal of Medicinal Chemistry|September 18, 1992
Development, synthesis, and biological evaluation of (-)-trans-(2S,5S)-2-[3-[(2-oxopropyl)sulfonyl]-4-n-propoxy-5-(3- hydroxypropoxy)-phenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent orally active platelet-activating factor (PAF) antagonist and its water-soluble prodrug phosphate esterN N Girotra, T Biftu, M M Ponpipom, et al.Journal of Medicinal Chemistry|November 11, 1994
Structure-activity relationships of C1 and C6 side chains of zaragozic acid A derivativesM M Ponpipom, N N Girotra, R L Bugianesi, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potentialM T Goulet, S R McAlpine, M J Staruch, et al.Biochemistry|April 23, 1999
Identification and biochemical characterization of a novel nortriterpene inhibitor of the human lymphocyte voltage-gated potassium channel, Kv1.3J P Felix, R M Bugianesi, W A Schmalhofer, et al.Transplantation|February 3, 1998
A tacrolimus-related immunosuppressant with reduced toxicityF J Dumont, S Koprak, M J Staruch, et al.Transplantation|February 3, 1998
A tacrolimus-related immunosuppressant with biochemical properties distinct from those of tacrolimusL B Peterson, J G Cryan, R Rosa, et al.Bioorganic & Medicinal Chemistry Letters|August 18, 1999
Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicityH M Armstrong, F Wong, M A Holmes, et al.Cellular Immunology|December 23, 1999
Correolide and derivatives are novel immunosuppressants blocking the lymphocyte Kv1.3 potassium channelsG C Koo, J T Blake, K Shah, et al.Pageof 2