Search Results - "RAMSEY, Gwendolyn"

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    Crystal structure of human cytosolic phosphoenolpyruvate carboxykinase reveals a new GTP-binding site by Dunten, Pete, Belunis, Charles, Crowther, Robert, Hollfelder, Kurt, Kammlott, Ursula, Levin, Wayne, Michel, Hanspeter, Ramsey, Gwendolyn B, Swain, Amy, Weber, David, Wertheimer, Stanley J

    Published in Journal of molecular biology (15-02-2002)
    “…We report crystal structures of the human enzyme phosphoenolpyruvate carboxykinase (PEPCK) with and without bound substrates. These structures are the first to…”
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    Discovery of benzothiazole-based adenosine A₂B receptor antagonists with improved A₂A selectivity by Firooznia, Fariborz, Cheung, Adrian Wai-Hing, Brinkman, John, Grimsby, Joseph, Gubler, Mary Lou, Hamid, Rachid, Marcopulos, Nicholas, Ramsey, Gwendolyn, Tan, Jenny, Wen, Yang, Sarabu, Ramakanth

    Published in Bioorganic & medicinal chemistry letters (01-04-2011)
    “…The highly potent but modestly selective N-(2-amino-4-methoxy-benzothiazol-7-yl)-N-ethyl-acetamide derivative 2 was selected as the starting point for the…”
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    Discovery of benzothiazole-based adenosine A sub(2B receptor antagonists with improved A) sub(2)A selectivity by Firooznia, Fariborz, Cheung, Adrian Wai-Hing, Brinkman, John, Grimsby, Joseph, Gubler, Mary Lou, Hamid, Rachid, Marcopulos, Nicholas, Ramsey, Gwendolyn, Tan, Jenny, Wen, Yang, Sarabu, Ramakanth

    Published in Bioorganic & medicinal chemistry letters (01-04-2011)
    “…The highly potent but modestly selective N-(2-amino-4-methoxy-benzothiazol-7-yl)-N-ethyl-acetamide derivative 2 was selected as the starting point for the…”
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    Journal Article
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    Discovery of benzothiazole-based adenosine A 2B receptor antagonists with improved A 2A selectivity by Firooznia, Fariborz, Cheung, Adrian Wai-Hing, Brinkman, John, Grimsby, Joseph, Gubler, Mary Lou, Hamid, Rachid, Marcopulos, Nicholas, Ramsey, Gwendolyn, Tan, Jenny, Wen, Yang, Sarabu, Ramakanth

    “…The highly potent but modestly selective N-(2-amino-4-methoxy-benzothiazol-7-yl)- N-ethyl-acetamide derivative 2 was selected as the starting point for the…”
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    Journal Article
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    C-8 Modifications of 3-alkyl-1,8-dibenzylxanthines as inhibitors of human cytosolic phosphoenolpyruvate carboxykinase by Pietranico, Sherrie L., Foley, Louise H., Huby, Nicholas, Yun, Weiya, Dunten, Pete, Vermeulen, John, Wang, Ping, Toth, Katherine, Ramsey, Gwendolyn, Gubler, Mary-Lou, Wertheimer, Stanley J.

    Published in Bioorganic & medicinal chemistry letters (15-07-2007)
    “…Enzyme and cellular assay results for a number of new modifications on the C-8 aminobenzyl unit are reported. Pyrazole sulfonic acid amide analogs are shown to…”
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    Modified 3-alkyl-1,8-dibenzylxanthines as GTP-competitive inhibitors of phosphoenolpyruvate carboxykinase by FOLEY, Louise H, PING WANG, DUNTEN, Pete, RAMSEY, Gwendolyn, GUBLER, Mary-Lou, WERTHEIMER, Stanley J

    Published in Bioorganic & medicinal chemistry letters (20-10-2003)
    “…The first non-substrate like inhibitors of human cytosolic phosphoenolpyruvate carboxykinase (PEPCK) competitive with GTP are reported. An effort to discover…”
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    X-ray structures of two xanthine inhibitors bound to PEPCK and N-3 modifications of substituted 1,8-dibenzylxanthines by FOLEY, Louise H, PING WANG, DUNTEN, Pete, RAMSEY, Gwendolyn, GUBLER, Mary-Lou, WERTHEIMER, Stanley J

    Published in Bioorganic & medicinal chemistry letters (03-11-2003)
    “…The analysis of the X-ray structures of two xanthine inhibitors bound to PEPCK and a comparison to the X-ray structure of GTP bound to PEPCK are reported. The…”
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