邻苯二酚-O-甲基转移酶
甲基转移酶
多巴胺
精神分裂症(面向对象编程)
儿茶酚
化学
激素
神经科学
多巴胺能
生物化学
甲基化
生物
心理学
精神科
基因
等位基因
作者
Giusy Tassone,Simone Carradori,Samuele Maramai,Ilaria D’Agostino
出处
期刊:Elsevier eBooks
[Elsevier]
日期:2023-09-08
卷期号:: 63-81
被引量:5
标识
DOI:10.1016/b978-0-12-823974-2.00029-2
摘要
Catechol-O-methyltransferase (COMT) is a magnesium-dependent enzyme responsible for the catalytic O-methylation reaction of endogenous catecholamines and neurotransmitters. It is also involved in the metabolic process of various hormones and drugs incorporating catecholic structures. COMT has become an attractive biological target in the central nervous system (CNS) disorders associated with dopamine depletion, such as Parkinson’s disease (PD), schizophrenia, and depression. In this chapter, we will provide a thorough description of COMT structural features and its physiopathological roles. Then, we will discuss the different generations of compounds proposed as COMT inhibitors from a medicinal chemistry perspective, including a structure-activity relationship analysis for the best-performing classes of analogues. In addition, updated information about the clinical benefits of the most relevant inhibitors will be highlighted.
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