amoscanate与曼氏血吸虫、盘尾丝虫和牛心脏中环amp -磷酸二酯酶的相互作用。

Tropenmedizin und Parasitologie Pub Date : 1984-06-01
R D Walter, E J Albiez
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引用次数: 0

摘要

驱虫化合物amoscanate(4-异硫氰酸酯-4'-硝基二苯胺)及其衍生物CGP 6140和CGP 8045是血吸虫和丝虫的环amp -磷酸二酯酶活性的有效抑制剂,也是牛心脏钙调素依赖性酶和非依赖性酶的有效抑制剂。如CGP 8045所示,对底物的抑制类型是非竞争性的,对寄生虫和哺乳动物酶的抑制常数在50微克/毫升范围内。有人提出,氨甘酸及其衍生物对环AMP-磷酸二酯酶活性的抑制——导致环AMP的积累——可能随后导致由环AMP依赖性蛋白激酶控制的代谢区域的调节紊乱,如糖原代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction of amoscanate with the cyclic AMP-phosphodiesterases from Schistosoma mansoni, Onchocerca volvulus and bovine heart.

The anthelmintic compounds amoscanate (4-isothiocyanato-4'-nitrodiphenylamine) and its derivatives CGP 6140 and CGP 8045 are potent inhibitors of the activities of cyclic AMP-phosphodiesterases from schistosomal and filarial worms as well as from both the calmodulin-dependent and the -independent enzyme of bovine heart. As shown for CGP 8045 the type of inhibition is non-competitive with respect to the substrate and the inhibition constants were determined to be in the range of 50 micrograms/ml for the enzymes of parasites and mammalian. It is proposed that the inhibition of cyclic AMP-phosphodiesterase-activity by amoscanate and derivatives - resulting in accumulation of cyclic AMP - might subsequently lead to disturbances in the regulation of metabolic areas like glycogen metabolism which are controlled by cyclic AMP-dependent protein kinases.

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