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咪唑烷二酮衍生物的明确合成及抗疟预防活性

Unambiguous synthesis and prophylactic antimalarial activities of imidazolidinedione derivatives.

作者信息

Zhang Quan, Guan Jian, Sacci John, Ager Arba, Ellis William, Milhous Wilbur, Kyle Dennis, Lin Ai J

机构信息

Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Silver Spring, Maryland 20910, USA.

出版信息

J Med Chem. 2005 Oct 6;48(20):6472-81. doi: 10.1021/jm0504252.

Abstract

WR182393, a guanidinoimidazolidinedione derivatives with potent causal prophylactic antimalarial activity by intramuscular injection, was previously prepared by treatment of chloroproguanil and diethyl oxalate, yielding a mixture of two closely related isomers. Poor solubility of the mixture made the separation and purification impossible. To overcome the separation problem, new and facile unambiguous syntheses of the two active components were reported. The new synthetic methods facilitate the synthesis of not only the active components, but also their derivatives. To search for compounds with good oral efficacy, a series of carbamate derivatives of the active components were prepared by the new procedure, many of which showed profound causal prophylactic antimalarial activity against Plasmodium yoelii in mouse by oral administration.

摘要

WR182393是一种胍基咪唑烷二酮衍生物,通过肌肉注射具有强效的病因性预防抗疟活性,它先前是由氯胍和草酸二乙酯反应制备的,得到了两种紧密相关的异构体的混合物。该混合物的溶解度差,使得分离和纯化无法进行。为了解决分离问题,人们报道了两种活性成分的新的、简便且明确的合成方法。这些新的合成方法不仅有助于活性成分的合成,也有助于其衍生物的合成。为了寻找具有良好口服疗效的化合物,通过新方法制备了一系列活性成分的氨基甲酸酯衍生物,其中许多通过口服给药对约氏疟原虫显示出强效的病因性预防抗疟活性。

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