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N-[4-(4'-硝基苯胺基)-苯基]-S-(β-羧乙基)-二硫代氨基甲酸酯与犬恶丝虫精氨酰-tRNA合成酶的寄生虫特异性相互作用。

Parasite-specific interaction of N-[4-(4'nitroanilino)-phenyl]-S-(beta-carboxyethyl)-dithiocar bamic acid-ester with arginyl-tRNA-synthetase from Dirofilaria immitis.

作者信息

Walter R D, Kuhlow F

出版信息

Trop Med Parasitol. 1985 Dec;36(4):230-2.

PMID:3841408
Abstract

A potent inhibition of arginyl-tRNA-synthetase from Dirofilaria immitis by N-[4-(4'nitroanilino)-phenyl]-S-(beta-carboxylethyl)-dith iocarbamic acid-ester (CGP 8065) is demonstrated, which indicates the charging of amino acids to tRNA as a possible target for the chemotherapeutic attack by this filaricidal compound. CGP 8065 competes with ATP; the inhibition constant was determined to be 13 micrograms ml-1 (34 microM). The Michaelis constants for arginine and ATP were found to be 5 microM and 0.4 mM, respectively. The inhibition of arginyl-tRNA-synthetase by CGP 8065 was shown to be specific for D. immitis; the isofunctional enzymes from Ascaris suum and rat liver were not affected.

摘要

已证实N-[4-(4'-硝基苯胺基)-苯基]-S-(β-羧乙基)-二硫代氨基甲酸酯(CGP 8065)对犬恶丝虫的精氨酰-tRNA合成酶有强烈抑制作用,这表明氨基酸与tRNA的结合可能是这种杀丝虫化合物化疗攻击的一个靶点。CGP 8065与ATP竞争;抑制常数测定为13微克/毫升(34微摩尔)。精氨酸和ATP的米氏常数分别为5微摩尔和0.4毫摩尔。CGP 8065对精氨酰-tRNA合成酶的抑制作用显示对犬恶丝虫具有特异性;来自猪蛔虫和大鼠肝脏的同功能酶不受影响。

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