Selective substrate-based inhibitors of mammalian dimethylarginine dimethylaminohydrolase

被引:55
作者
Rossiter, S
Smith, CL
Malaki, M
Nandi, M
Gill, H
Leiper, JM
Vallance, P
Selwood, DL
机构
[1] UCL, BHF Labs, Div Med, Ctr Clin Pharmacol & Therapeut, London WC1E 6JF, England
[2] UCL, Wolfson Inst Biomed Res, Dept Biol & Med Chem, London WC1E 6BT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1021/jm050187a
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The enzyme DDAH metabolizes methylarginines that are inhibitors of nitric oxide synthase (NOS). Substrate-based inhibitors of mammalian DDAH have been synthesized, with optimization to give selective inhibition of DDAH with no significant direct effect on NOSs. These are the first examples of reversible DDAH inhibitors with significant activity and selectivity. In vivo administration increases plasma ADMA levels, giving proof of concept that these inhibitors can be used to probe the physiological effects of DDAH inhibition, with potential for pharmaceutical use of DDAH inhibitors in diseases where excess NO production is implicated.
引用
收藏
页码:4670 / 4678
页数:9
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