Highly selective aldose reductase inhibitors .1. 3-(Arylalkyl)-2,4,5-trioxoimidazolidine-1-acetic acids

被引:38
作者
Ishii, A
Kotani, T
Nagaki, Y
Shibayama, Y
Toyomaki, Y
Okukado, N
Ienaga, K
Okamoto, K
机构
[1] Institute of Bio-Active Science, Nippon Zoki Pharmaceutical Co., Ltd., Kato-gun 673-14, Kinashi, Yashiro-cho
关键词
D O I
10.1021/jm9508393
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 3-(arylalkyl)-2,4,5-trioxoimidazolidine-1-acids (1) was prepared and tested for aldose reductase (AR) and aldehyde reductase (ALR) inhibitory activities. These compounds showed strong inhibitory activity against AR without significant inhibitory activity for ALR. The ratio of IC50(ALR)/IC50(AR) was > 1000 in some compouds. On the basis of pharmacological tests such as the recovery of reduced motor nerve conduction velocity and toxicological profile, 3-(3-nitrobenzyl)-2,4,5-trioxoimidazolidine-1-acid (NZ-314) was selected as the candidate for clinical development.
引用
收藏
页码:1924 / 1927
页数:4
相关论文
共 21 条