共 124 条
Blocking NO synthesis: How, where and why?
被引:286
作者:

Vallance, P
论文数: 0 引用数: 0
h-index: 0
机构:
UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England

Leiper, J
论文数: 0 引用数: 0
h-index: 0
机构:
UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England
机构:
[1] UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England
基金:
英国惠康基金;
关键词:
D O I:
10.1038/nrd960
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Nitric oxide (NO) is a key physiological mediator, and the association of disordered NO generation with many pathological conditions has led to much interest in pharmacologically modulating NO levels. However, the wide range of processes in which NO has been implicated, and the fact that increases or decreases in NO levels might be therapeutically desirable depending on the condition or even at different stages of the same condition, pose considerable challenges for drug development. Here, we focus on the rationale and potential for approaches that reduce NO synthesis, which have led to the development of several compounds that will shortly be entering clinical trials.
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页码:939 / 950
页数:12
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