首页> 外文期刊>Arzneimittel-Forschung: =Drug Research >Epoxyethane-/ethynesulfonamides with antifilarial activities. Degradation kinetics and inhibitory effect on filarial malate dehydrogenase and lactate dehydrogenase.
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Epoxyethane-/ethynesulfonamides with antifilarial activities. Degradation kinetics and inhibitory effect on filarial malate dehydrogenase and lactate dehydrogenase.

机译:具有抗丝活性的环氧乙烷/乙炔磺酰胺。对丝状苹果酸脱氢酶和乳酸脱氢酶的降解动力学和抑制作用。

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Some epoxyethane-/ethynesulfonamides had shown strong filaricidal activity with inconstant reproducibility as a result of a lack of stability in aqueous solution. The degradation in hydroxylic and aprotic solutions of two epoxyethanesulfonamides and one ethynesulfonamide was investigated using TLC, HPLC, GC and mass spectrometry. For both epoxydes, the degradation rate followed first-order kinetics and was more rapid in hydroxylic than in aprotic solutions. The degradation increased with the temperature whereas it was not modified with and without light exposure. Four kinds of degradation products were found: the first one involved the oxidation of the epoxyde bond, the second the breaking of the N-S bond, the third a desulfonation product and the fourth was not identified. In contrast, the stability of ethynesulfonamide was better than those of epoxyethanesulfonamide. These results suggest that epoxyethanesulfonamides should be kept at +4 degrees C before being injected to animals during the study of biological activity. Since epoxyde compounds are known to have inhibitory effects on parasite energy metabolism enzymes, the compunds were evaluated on two major filarial enzymes: lactate dehydrogenase (LDH) and cytoplasmic malate dehydrogenase (MDH). Both epoxyethanesulfonamides showed only a slight inhibitory effect on filarial LDH and MDH confirming the evidence that the main mode of action of these compounds remains to discover. Moreover, ethynesulfonamide and the degradation products of both epoxyethane-sulfonamides had no effect on LDH and MDH.
机译:由于在水溶液中缺乏稳定性,一些环氧乙烷/乙炔磺酰胺显示出很强的杀菌活性,并且再现性不稳定。使用TLC,HPLC,GC和质谱法研究了两种环氧乙烷磺酰胺和一种乙磺酰胺在羟基和非质子溶液中的降解。对于两种环氧,降解速率均遵循一级动力学,并且在羟基化合物中的降解速度要比在非质子溶液中的降解速度更快。降解随温度增加而增加,而在暴露和不暴露的情况下均未改变。发现了四种降解产物:第一种涉及环氧键的氧化,第二种涉及N-S键的断裂,第三种涉及脱硫产物,第四种未被鉴定。相反,乙炔磺酰胺的稳定性优于环氧乙烷磺酰胺。这些结果表明,在进行生物活性研究期间,在将环氧乙烷磺酰胺注射到动物体内之前,应将其保持在+4摄氏度。由于已知环氧化合物对寄生虫能量代谢酶具有抑制作用,因此对两种主要的丝状酶进行了评估:乳酸脱氢酶(LDH)和细胞质苹果酸脱氢酶(MDH)。两种环氧乙烷磺酰胺仅对丝状LDH和MDH表现出轻微的抑制作用,从而证实了这些化合物的主要作用方式尚待发现的证据。而且,乙炔磺酰胺和两种环氧乙烷-磺酰胺的降解产物对LDH和MDH没有影响。

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