Novel lipoic acid analogues that inhibit nitric oxide synthase

被引:45
作者
Harnett, JJ
Auguet, M
Viossat, I
Dolo, C
Bigg, D
Chabrier, PE
机构
[1] Inst Henri Beaufour, Beaufour Ipsen Res Labs, Dept Med Chem, F-91966 Les Ulis, France
[2] Inst Henri Beaufour, Beaufour Ipsen Res Labs, Dept Biol, F-91966 Les Ulis, France
关键词
D O I
10.1016/S0960-894X(02)00216-0
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The synthesis and biological activity of novel lipoic acid analogues are reported. Lipoic acid and structural homologues coupled to arylthiophene amidine via carboxamide linkers are metabolic antioxidants capable of protecting neuronal cells against glutamate cytotoxicity, preventing loss of intracellular glutathione, and inhibit nitric oxide synthase. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:1439 / 1442
页数:4
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