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3-芳基-7-氯-3,4-二氢吖啶-1,9-(2H,10H)-二酮的抗疟和抗球虫活性。1-亚胺、1-胺、1-肟、1-腙及相关化合物。

Antimalarial and anticoccidial activity of 3-aryl-7-chloro-3,4-dihydroacridine-1,9-(2H,10H)-diones. 1-Imines, 1-amines, 1-oximes, 1-hydrazones and related compounds.

作者信息

Winkelmann E, Raether W

机构信息

Department of Drug Synthesis, Hoechst Aktiengesellschaft, Frankfurt/Main, Fed. Rep. of Germany.

出版信息

Arzneimittelforschung. 1987 Jun;37(6):647-61.

PMID:3311052
Abstract

Out of more than 130 synthesized derivatives of floxacrine and of 10-deoxyfloxacrine, such as 3-(4-trifluoromethyl-phenyl) or 3-(4-chlorophenyl)-7-chloro-10-hydroxy- or -10-deoxy-3,4-dihydroacridine- 1,9(2H,10H)-dione 1-imines and 1-hydrazones, more than 45 showed an activity against asexual stages of Plasmodium berghei in the mouse which was comparable with or superior to that of floxacrine. More than 25 derivatives of the 3-(4-chlorophenyl)-floxacrine series and 3-(4-chlorophenyl)-10-deoxy-floxacrine series are more effective than floxacrine against Eimeria tenella infection in chickens. 1-Amino compounds of the various series proved of be generally inactive, as did fragments of the structure of and compounds related to floxacrine. Structure-activity relations are suggested on the basis of examples.

摘要

在130多种合成的氟氯吖啶和10-脱氧氟氯吖啶衍生物中,如3-(4-三氟甲基苯基)或3-(4-氯苯基)-7-氯-10-羟基或-10-脱氧-3,4-二氢吖啶-1,9(2H,10H)-二酮1-亚胺和1-腙,超过45种对伯氏疟原虫在小鼠体内的无性阶段表现出活性,其活性与氟氯吖啶相当或优于氟氯吖啶。3-(4-氯苯基)-氟氯吖啶系列和3-(4-氯苯基)-10-脱氧-氟氯吖啶系列的25种以上衍生物在对抗鸡的柔嫩艾美耳球虫感染方面比氟氯吖啶更有效。各系列的1-氨基化合物通常被证明无活性,与氟氯吖啶结构相关的化合物片段也是如此。根据实例提出了构效关系。

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