多巴胺
化学
单加氧酶
酶
基质(水族馆)
去甲肾上腺素
儿茶酚胺
药理学
生物化学
医学
神经科学
生物
细胞色素P450
生态学
作者
А. Н. Беляев,Humberto Ferreira,David A. Learmonth,Patrı́cio Soares-da-Silva
出处
期刊:Current Enzyme Inhibition
[Bentham Science Publishers]
日期:2009-01-30
卷期号:5 (1): 27-43
被引量:27
标识
DOI:10.2174/157340809787314265
摘要
Dopamine β-monooxygenase (DBM) catalyses the conversion of dopamine to norepinephrine in the catecholamine biosynthetic pathway. The substrate specificity of DBM is wide and the enzyme is capable of performing a variety of oxidations. While the crystal structure of DBM is not yet available, various indirect data allow insight into the enzymes machinery. Considered an attractive therapeutic target for the treatment of hypertension and congestive heart failure, DBM and its inhibitors have received attention by medicinal chemists over the last four decades. Although several QSAR models for DBM inhibitors have been generated, these models are actually unable to explain the exceptionally high potency of the latest generation of inhibitors. Keywords: Dopamine β-monooxygenase, dopamine β-hydroxylase, inhibitor, imidazolethione, nepicastat, BIA 5-453, CHF
科研通智能强力驱动
Strongly Powered by AbleSci AI