Synthetic atpenin analogs: Potent mitochondrial inhibitors of mammalian and fungal succinate-ubiquinone oxidoreductase

被引:11
|
作者
Selby, Thomas P. [1 ]
Hughes, Kenneth A. [1 ]
Rauh, James J. [1 ]
Hanna, Wayne S. [1 ]
机构
[1] DuPont Crop Protect, Stine Haskell Res Ctr, Newark, DE 19711 USA
关键词
Synthetic atpenin analogs; Mitochondrial electron transport; Succinate-ubiquinone oxidoreductase; Complex II inhibition; Pentasubstituted pyridines; COMPLEX-II; PENICILLIUM SP; BINDING SITE; DEHYDROGENASE; REDUCTASE; ACID;
D O I
10.1016/j.bmcl.2010.01.066
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Atpenins and harzianopyridone represent a unique class of penta-substituted pyridine-based natural products that are potent inhibitors of complex II (succinate-ubiquinone oxidoreductase) in the mitochondrial respiratory chain. These compounds block electron transfer in oxidative phosphorylation by inhibiting oxidation of succinate to fumarate and the coupled reduction of ubiquinone to ubiquinol. From our investigations of complex II inhibitors as potential agricultural fungicides, we report here on the synthesis and complex II inhibition for a series of synthetic atpenin analogs against both mammalian and fungal forms of the enzyme. Synthetic atpenin 2e provided optimum mammalian and fungal inhibition with slightly higher potency than natural occurring atpenin A5. (C) 2010 Elsevier Ltd. All rights reserved.
引用
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页码:1665 / 1668
页数:4
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