Nebicapone (BIA 3-202) 是一种可逆的儿茶酚-O-甲基转移酶 (COMT) 抑制剂，主要通过葡萄糖醛酸化代谢。Nebicapone 主要是外周作用的抑制剂，通过抑制 COMT 降低 L-DOPA 向 3-O-甲基-DOPA 的生物转化，Nebicapone 可用于帕金森病的研究。
货号:ajcx39064
CAS:274925-86-9
分子式:C14H11NO5
分子量：273.24
溶解度:N/A
纯度：98%
存储：Store at -20°C
库存：现货

Background:

Nebicapone (BIA 3-202), a reversible catechol-O-methyltransferase (COMT) inhibitor, is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of COMT, and it is potential for the treatment of Parkinson's disease[1].

[1]. Loureiro AI, et al. Human metabolism of nebicapone (BIA 3-202), a novel catechol-o-methyltransferase inhibitor: characterization of in vitro glucuronidation. Drug Metab Dispos. 2006 Nov;34(11):1856-62.