Search Results - "Britcher, Susan F"

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    HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: An investigation into the role of the P1' side chain on structure-activity by Young, Steven D, Payne, Linda S, Thompson, Wayne J, Gaffin, Neil, Lyle, Terry A, Britcher, Susan F, Graham, Samuel L, Schultz, Thomas H, Deana, Albert A

    Published in Journal of medicinal chemistry (01-05-1992)
    “…A systematic investigation was undertaken to determine the role of the P1' sidechain in a series of hydroxyethylene isostere based inhibitors of HIV-1…”
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    Journal Article
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    Structure and activity of hydrogenated derivatives of (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801) by Lyle, Terry A, Magill, Catherine A, Britcher, Susan F, Denny, George H, Thompson, Wayne J, Murphy, Joan S, Knight, Antony R, Kemp, John A, Marshall, George R

    Published in Journal of medicinal chemistry (01-03-1990)
    “…Several hydrogenated derivatives of the potent NMDA antagonist 1 have been prepared and evaluated as competitive inhibitors of [3H]-1 binding. These compounds…”
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    Synthesis and orexigenic activity of some 1-methyl-4-piperidylidene-substituted pyrrolo[2,1-b][3]benzazepine and dibenzocycloheptene derivatives by Remy, David C, Britcher, Susan F, Anderson, Paul S, Belanger, Patrice C, Girard, Yves, Clineschmidt, B. V

    Published in Journal of medicinal chemistry (01-03-1982)
    “…The synthesis and orexigenic activity of some unsubstituted and Bz-carboxylic acid substituted 1-methyl-4-piperidylidenepyrrolo[2,1-b][3]benzazepine and…”
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    2-Heterocyclic indole-3-sulfones as inhibitors of HIV-1 reverse transcriptase by Young, Steven D., Amblard, Muriel C., Britcher, Susan F., Grey, Vanessa E., Tran, Lee O., Lumma, William C., Huff, Joel R., Schleif, William A., Emini, Emilio E., O'Brien, Julie A., Pettibone, Douglas J.

    Published in Bioorganic & medicinal chemistry letters (02-03-1995)
    “…A variety of 2-heterocycle substituted 3-phenysulfonyl-5-chloroindoles were investigated as replacements for the 2-carboxamide functionality of the potent…”
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    Journal Article