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2-胍基-4-氧代咪唑啉衍生物的合成及抗疟活性。

Synthesis and antimalarial activity of 2-guanidino-4-oxoimidazoline derivatives.

机构信息

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

出版信息

J Med Chem. 2011 Jul 14;54(13):4523-35. doi: 10.1021/jm200111g. Epub 2011 May 31.

Abstract

A series of 2-guanidino-4-oxoimidazoline (deoxo-IZ) derivatives was prepared and showed potent antimalarial activities in rodent and Rhesus models. Compound 8e, the most potent analogues of this series, is the first non-8-aminoqinoline antimalarial that demonstrated radical curative activity in non-human primate by oral route and showed causal prophylactic activity comparable to that of the commonly used clinical drugs in Rhesus monkeys infected with sporozoites of Plasmodium cynomolgi. The metabolic stability and metabolites profile indicated that the new deoxo-IZ derivatives (8) may act as prodrugs of the corresponding IZ (1 and 2) derivatives.

摘要

一系列 2-胍基-4-氧代咪唑啉(去氧 IZ)衍生物被制备出来,并在啮齿动物和恒河猴模型中表现出很强的抗疟活性。化合物 8e 是该系列中最有效的类似物,它是第一个非 8-氨基喹啉类抗疟药,通过口服途径在非人类灵长类动物中显示出根治活性,并表现出与常用临床药物相当的因果预防活性,在感染疟原虫孢子的恒河猴中。代谢稳定性和代谢产物谱表明,新型去氧 IZ 衍生物(8)可能是相应 IZ(1 和 2)衍生物的前药。

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