Search Results - "Wilkerson, WW"

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  1. 1

    A quantitative structure—activity relationship analysis of a series of 2′-(2,4-difluorophenoxy)-4′-substituted methanesulfonilides by Wilkerson, WW

    “…A series of antiinflammatory 2′-(2,4-difluorophenoxy)-4′-substituted methanesulfonilides was subjected to quantitative structure—activity relationship (QSAR)…”
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    Journal Article
  2. 2

    Acetylcholine release enhancers related to linopirdine: A structure—activity relationship study. II by Wilkerson, WW, Earl, RA, Calabrese, JC, Drammond, S, Teleha, CA, Voss, ME, Zaczek, R

    “…Several series of α,α-disubstituted polycyclic compounds were found to enhance the stimulus-induced release of neurotransmitters, especially acetylcholine, in…”
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  3. 3

    Antiinflammatory 4,5-Diarylpyrroles. 2. Activity as a Function of Cyclooxygenase-2 Inhibition by Wilkerson, Wendell Wilkie, Copeland, Robert A, Covington, Maryanne, Trzaskos, James M

    Published in Journal of medicinal chemistry (01-09-1995)
    “…The antiinflammatory activity of a series of 2-substituted- and 2,3-disubstituted-4-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-1H- pyrroles was previously…”
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    Journal Article
  4. 4

    Nonsymmetrically Substituted Cyclic Urea HIV Protease Inhibitors by Wilkerson, Wendell W, Dax, Scott, Cheatham, Walter W

    Published in Journal of medicinal chemistry (05-12-1997)
    “…A series of nonsymmetrically substituted cyclic ureacarboxamides was synthesized and evaluated for antiviral activity as a function of the inhibition of…”
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  5. 5

    HIV Protease Inhibitory Bis-benzamide Cyclic Ureas:  A Quantitative Structure−Activity Relationship Analysis by Wilkerson, Wendell W, Akamike, Emeka, Cheatham, Walter W, Hollis, Andrea Y, Collins, R. Dale, DeLucca, Indawati, Lam, Patrick Y. S, Ru, Yu

    Published in Journal of medicinal chemistry (11-10-1996)
    “…A series of N,N‘-disubstituted cyclic urea 3-benzamides has been synthesized and evaluated for HIV protease inhibition and antiviral activity. Some of these…”
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  6. 6

    Antiinflammatory 4,5-Diarylpyrroles: Synthesis and QSAR by Wilkerson, Wendell W, Galbraith, William, Gans-Brangs, Kathleen, Grubb, Mary, Hewes, Walter E, Jaffee, Bruce, Kenney, J. P, Kerr, Janet, Wong, Nancy

    Published in Journal of medicinal chemistry (01-04-1994)
    “…A series of 2-substituted- and 2,3-disubstituted-4-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-1H- pyrroles was synthesized and found to be active in the rat…”
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    Journal Article
  7. 7

    A bis-[N-3-(1-hydroxy-1-methyl-ethyl)-benzyl)-cyclic urea as a HIV protease inhibitor by Wilkerson, Wendell W., Hollis, Andrea Y., Cheatham, Walter W., Lam, Gilbert N., Erickson-Viitanen, Susan, Bacheler, Lee, Cordova, Beverly C., Klabe, Ronald M., Meek, James L.

    Published in Bioorganic & medicinal chemistry letters (21-12-1995)
    “…Synthetic efforts to overcome the metabolic oxidative degradation of the HIV protease inhibitory cyclic urea DMP323, a benzyl alcohol, have led to the…”
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  8. 8

    3-Substituted 3-(4-pyridinylmethyl)-1,3-dihydro-1-phenyl-2H-indol-2-ones as acetylcholine release enhancers: synthesis and SAR by Wilkerson, Wendell W, Kergaye, Ahmed A, Tam, S. William

    Published in Journal of medicinal chemistry (01-10-1993)
    “…A series of 3-substituted, 3-(4-pyridinylmethyl)-1,3-dihydro-1-phenyl-2H-indol-2-ones was synthesized and found to enhance the stimulus-induced release of…”
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    Bovine prothrombin fragment 1, segment 1-10. Synthesis and immunological investigation by Ten Kortenaar, P B, Wilkerson, W W, Boggs, 3rd, N T, Madar, D A, Koehler, K A, Hiskey, R G

    “…The N-terminal decapeptide methyl ester, H-Ala-Asn-Lys-Gly-Phe-Leu-Gla-Gla-Val-Arg-OCH3 (16) of bovine prothrombin fragment 1 has been prepared by standard…”
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