Search Results - "Klingbeil, Kristina M"

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    The antitumor activity of novel pyrazoloquinoline derivatives by Wentland, Mark P., Aldous, Suzanne C., Gruett, Monte D., Perni, Robert B., Powles, Ronald G., Danz, Deborah W., Klingbeil, Kristina M., Peverly, A.Danielle, Robinson, Ronald G., Corbett, Thomas H., Rake, James B., Coughlin, Susan A.

    Published in Bioorganic & medicinal chemistry letters (16-02-1995)
    “…Mammalian topoisomerase II inhibition activity has been identified in a series of novel pyrazoloquinoline derivatives; potency for two analogues containing…”
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    3-benzyl-quinolones: Novel, potent inhibitors of mammalian topoisomerase II by Eissenstat, Michael A., Kuo, Gee-Hong, Weaver, John D., Wentland, Mark P., Robinson, Ronald G., Klingbeil, Kristina M., Danz, Deborah W., Corbett, Thomas H., Coughlin, Susan A.

    Published in Bioorganic & medicinal chemistry letters (04-05-1995)
    “…Replacement of the 3-carboxy group of quinolone topoisomerase II inhibitors by hydroxy substituted benzyl groups resulted in potent topoisomerase II…”
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    Cyclic variations of SR 233377 (WIN 33377) and effects on antitumor activity by Wentland, Mark P., Perni, Robert B., Huang, Jianhua I., Powles, Ronald G., Aldous, Suzanne C., Klingbeil, Kristina M., Danielle Peverly, A., Robinson, Ronald G., Corbett, Thomas H., Jones, Julie L., Rake, James B., Coughlin, Susan A.

    Published in Bioorganic & medicinal chemistry letters (18-06-1996)
    “…Novel derivatives of SR 233377 ( 1, WIN 33377) where a pyrazolo ring fusion has been incorporated at the 1- and 9-positions of the thioxanthone ring displayed…”
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    Potent mammalian topoisomerase II inhibitors: 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(2,6-dimethyl-4-pyridinyl)-4-substituted-quinolines by Kuo, Gee-Hong, Eissenstat, Michael A., Wentland, Mark P., Robinson, Ron G., Klingbeil, Kristina M., Danz, Debbie W., Coughlin, Susan A.

    Published in Bioorganic & medicinal chemistry letters (16-02-1995)
    “…A series of novel 4-substituted-1,4-dihydro-quinolines 3 were prepared and found to exhibit moderate to excellent mammalian topo II inhibitory activity. Among…”
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