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高选择性醛糖还原酶抑制剂。1. 3-(芳基烷基)-2,4,5-三氧代咪唑烷-1-乙酸

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

作者信息

Ishii A, Kotani T, Nagaki Y, Shibayama Y, Toyomaki Y, Okukado N, Ienaga K, Okamoto K

机构信息

Institute of Bio-Active Science, Nippon Zoki Pharmaceutical Company, Ltd., Kato-gun, Japan.

出版信息

J Med Chem. 1996 Apr 26;39(9):1924-7. doi: 10.1021/jm9508393.

Abstract

A series of 3-(arylalkyl)-2,4,5-trioxoimidazolidine-1-acetic 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 compounds. 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-acetic acid (NZ-314) was selected as the candidate for clinical development.

摘要

制备了一系列3-(芳基烷基)-2,4,5-三氧代咪唑烷-1-乙酸(1),并测试了它们对醛糖还原酶(AR)和醛还原酶(ALR)的抑制活性。这些化合物对AR表现出强抑制活性,而对ALR没有显著抑制活性。在某些化合物中,IC50(ALR)/IC50(AR)的比值>1000。基于诸如恢复降低的运动神经传导速度和毒理学特征等药理学测试,选择3-(3-硝基苄基)-2,4,5-三氧代咪唑烷-1-乙酸(NZ-314)作为临床开发候选药物。

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