4-phenyl-4-oxo-butanoic acid derivatives inhibitors of kynurenine 3-hydroxylase

被引:23
作者
Giordani, A
Pevarello, P
Cini, M
Bormetti, R
Greco, F
Toma, S
Speciale, C
Varasi, M
机构
[1] Pharmacia & Upjohn Inc, Dept Chem, I-20014 Milan, Italy
[2] Pharmacia & Upjohn Inc, CNS Biol, I-20014 Milan, Italy
[3] Pharmacia & Upjohn Inc, CFO, Proc R&D, I-20014 Milan, Italy
[4] Pharmacia & Upjohn Inc, Dept Biol, I-20014 Milan, Italy
关键词
enzyme inhibition; kynurenine; hydroxylase; neuroprotection; stereoselectivity;
D O I
10.1016/S0960-894X(98)00517-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Kynurenine 3-hydroxylase (KYN 3-OHase) is a key enzyme in the kynurenine pathway of tryptophan degradation and its inhibition may be an effective mechanism for counteracting neuronal excitotoxic damage. We present here a new class of inhibitors derived from a structure-activity relationship (SAR) study of the benzoylalanine side-chitin of 1. 2-hydroxy-4-(3,4-dichlorophenyl)-4-oxo-butanoic acid (8) and 2-benzyl-4-(3,4-dichlorophenyl)-4-oxo-butanoic acid (10) emerged as the most interesting derivatives. Enantiospecific synthesis for both enantiomers of 8 and diastereomeric salt resolution for those of 10 were successfully applied. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2907 / 2912
页数:6
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