Search Results - "Belonga, Kenneth L."

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    Novel 21-aminosteroids that inhibit iron-dependent lipid peroxidation and protect against central nervous system trauma by Jacobsen, E. Jon, McCall, John M, Ayer, Donald E, VanDoornik, Fred J, Palmer, John R, Belonga, Kenneth L, Braughler, J. Mark, Hall, Edward D, Houser, David J

    Published in Journal of medicinal chemistry (01-04-1990)
    “…A novel class of 21-aminosteroids has been developed. Compounds within this series are potent inhibitors of iron-dependent lipid peroxidation in rat brain…”
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    Journal Article
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    2-(Aminomethyl)chromans that inhibit iron-dependent lipid peroxidation and protect against central nervous system trauma and ischemia by Jacobsen, E. Jon, VanDoornik, Fred J, Ayer, Donald E, Belonga, Kenneth L, Braughler, J. Mark, Hall, Edward D, Houser, David J

    Published in Journal of medicinal chemistry (01-11-1992)
    “…A series of 2-(aminomethyl)chromans was developed as potent inhibitors of iron-dependent lipid peroxidation. Compounds within this class are extremely…”
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    Journal Article
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    Piperazine Imidazo[1,5-a]quinoxaline Ureas as High-Affinity GABAA Ligands of Dual Functionality by Jacobsen, E. Jon, Stelzer, Lindsay S, TenBrink, Ruth E, Belonga, Kenneth L, Carter, Donald B, Im, Haesook K, Im, Wha Bin, Sethy, Vimala H, Tang, Andy H, VonVoigtlander, Philip F, Petke, James D, Zhong, Wei-Zhu, Mickelson, John W

    Published in Journal of medicinal chemistry (08-04-1999)
    “…A series of imidazo[1,5-a]quinoxaline piperazine ureas appended with a tert-butyl ester side chain at the 3-position was developed. Analogues within this…”
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    Journal Article
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    3-Phenyl-Substituted Imidazo[1,5-a]quinoxalin-4-ones and Imidazo[1,5-a]quinoxaline Ureas That Have High Affinity at the GABAA/Benzodiazepine Receptor Complex by Jacobsen, E. Jon, Stelzer, Lindsay S, Belonga, Kenneth L, Carter, Donald B, Im, Wha Bin, Sethy, Vimala H, Tang, Andrew H, VonVoigtlander, Philip F, Petke, James D

    Published in Journal of medicinal chemistry (13-09-1996)
    “…A series of imidazo[1,5-a]quinoxalin-4-ones and imidazo[1,5-a]quinoxaline ureas containing substituted phenyl groups at the 3-position was developed. Compounds…”
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    Journal Article
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