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通过与α-(2,4,5,7-四硝基-9-芴叉亚胺基氧基)丙酸形成复合物来解析抗疟药物。

Resolution of antimalarial agents via complex formation with alpha-(2,4,5,7-tetranitro-9-fluorenylideneaminooxy) propionic acid.

作者信息

Carroll F I, Berrang B, Linn C P

出版信息

J Med Chem. 1978 Apr;21(4):326-30. doi: 10.1021/jm00202a002.

Abstract

The resolution of several antimalarial agents via pi-complex formation with alpha-(2,4,5,7-tetranitro-9-fluorenylideneaminooxy) propionic acid (TAPA) is reported. Since this represents the first use of this agent for the resolution of amines, some details of the separations are presented. The method proved successful for resolving weakly alkaline amines that did not form stable salts with common resolving acids, highly insoluble amines that did not form soluble salts with usual resolving acids, and amines that did not form crystalline salts with commonly available resolving acids. The optical isomers of several antimalarial agents were evaluated against Plasmodium berghei in the mouse. None of the optically active forms showed any significant differences. The curative activity of (+)- and (-)-primaquine against Plasmodium cynomolgi in the rhesus monkey was essentially identical; however, significant differences in toxicity were noted.

摘要

据报道,几种抗疟药通过与α-(2,4,5,7-四硝基-9-芴叉亚氨基氧基)丙酸(TAPA)形成π络合物来拆分。由于这是该试剂首次用于胺的拆分,因此给出了一些分离细节。该方法被证明对于拆分与常用拆分酸不形成稳定盐的弱碱性胺、与常用拆分酸不形成可溶性盐的高度不溶性胺以及与常用拆分酸不形成结晶盐的胺是成功的。在小鼠中评估了几种抗疟药的光学异构体对伯氏疟原虫的作用。没有一种光学活性形式显示出任何显著差异。(+)-和(-)-伯氨喹对恒河猴食蟹猴疟原虫的治疗活性基本相同;然而,在毒性方面发现了显著差异。

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