Search Results - "Harris, Ralph N."

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    Highly potent, non-basic 5-HT6 ligands. Site mutagenesis evidence for a second binding mode at 5-HT6 for antagonism by Harris, Ralph N., Stabler, Russel S., Repke, David B., Kress, James M., Walker, Keith A., Martin, Renee S., Brothers, Julie M., Ilnicka, Mariola, Lee, Simon W., Mirzadegan, Tara

    Published in Bioorganic & medicinal chemistry letters (01-06-2010)
    “…A series of 5-HT6 ligands derived from (R)-1-(amino)methyl-6-(phenyl)sulfonyltetralin was prepared that yielded several neutral, non-basic analogs having…”
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    Journal Article
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    Quaternary salts of 2-[(hydroxyimino)methyl]imidazole. 4. Effect of various side-chain substituents on therapeutic activity against anticholinesterase intoxication by Goff, Dane A, Koolpe, Gary A, Kelson, Andrew B, Vu, Huynh M, Taylor, Dorris L, Bedford, Clifford D, Harris, Ralph N, Mussalam, H. A, Koplovitz, Irwin

    Published in Journal of medicinal chemistry (01-04-1991)
    “…A series of quaternary salt derivatives of 2-[(hydroxyimino)methyl]-1-methylimidazole incorporating various side chains bearing ether, silyl, nitrile, ester,…”
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    Journal Article
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    Highly potent, non-basic 5-HT sub(6) ligands. Site mutagenesis evidence for a second binding mode at 5-HT sub(6) for antagonism by Harris, Ralph N, Stabler, Russel S, Repke, David B, Kress, James M, Walker, Keith A, Martin, Renee S, Brothers, Julie M, Ilnicka, Mariola, Lee, Simon W, Mirzadegan, Tara

    Published in Bioorganic & medicinal chemistry letters (01-06-2010)
    “…A series of 5-HT sub(6) ligands derived from (R)-1-(amino)methyl-6-(phenyl)sulfonyltetralin was prepared that yielded several non-basic analogs having…”
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    Journal Article
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    Structure-activity relationships for reactivators of organophosphorus-inhibited acetylcholinesterase: quaternary salts of 2-[(hydroxyimino)methyl]imidazole by BEDFORD, C. D, HARRIS, R. N. III, HOWD, R. A, MILLER, A, NOLEN, H. W. III, KENLEY, R. A

    Published in Journal of medicinal chemistry (01-11-1984)
    “…A series of 1,3-disubstituted-2-[(hydroxyimino)methyl]imidazolium halides were prepared and evaluated in vitro with respect to their ability to reactivate…”
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    Journal Article