Antifilarial and trypanocidal properties of phenothiazines and related polycyclics as new lead structures

被引:16
作者
Loiseau, PM [1 ]
Mettey, Y [1 ]
Vierfond, JM [1 ]
机构
[1] UNIV POITIERS, FAC PHARM, F-86000 POITIERS, FRANCE
关键词
Molinema dessetae; Trypanosoma brucei brucei; antifilarial; phenothiazine derivatives;
D O I
10.1016/S0020-7519(96)00062-8
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
New phenothiazine derivatives and 4 related lead structures have been studied for their antifilarial and trypanocidal properties. Regarding phenothiazine derivatives, the nitrile group at the 3 position on the phenothiazine ring had a strong in vitro antifilarial effect against Molinema dessetae infective larvae. Among the 4 new lead structures, compound 4 or naphtho(2',3': 4,5)thiazolo(3,2-a)benzimidazole-7,12-dione was the most antifilarial, with IC50 of 8 mu M at day 8. These results justify further studies in vivo. A slight effect was observed against the trypanosomes maintained in vitro since minimum inhibitory concentrations of active compounds were 50 mu M after a 24-h incubation period. Nevertheless, no trypanocidal activity was observed in vivo after a 100 mg kg(-1) treatment and the compound 3 or dibenzo(b,f)(1,4)thiazine-11-amine was lethal at this dose. These new lead structures have now to be optimised using pharmaco-modulations. Copyright (C) 1996 Australian Society for Parasitology. Published by Elsevier Science Ltd.
引用
收藏
页码:1115 / 1117
页数:3
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