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Tolcapone-d4
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Tolcapone-d4图片
CAS NO:1246816-93-2
包装与价格:
包装价格(元)
1mg电议
10mg电议

产品名称
Ro 40-7592-d4
产品介绍
Tolcapone-d4 (Ro 40-7592-d4) 是 Tolcapone 的氘代物。Tolcapone (Ro 40-7592) 是一种选择性,有效的,具有口服活性的外周和中枢COMT抑制剂,在肝脏中对 COMT 的IC50为 773 nM。Tolcapone 还是一种 α-syn 和 Aβ42 寡聚和原纤维形成的有效抑制剂。Tolcapone 诱导氧化应激导致神经母细胞瘤细胞凋亡(apoptosis) 和抑制肿瘤生长。
生物活性

Tolcapone-d4 (Ro 40-7592-d4) is the deuterium labeled Tolcapone. Tolcapone (Ro 40-7592) is a selective, orally active and powerful mixed (peripheral and central)COMTinhibitor with anIC50of 773 nM in the liver[1]. Tolcapone is also a potent inhibitor of α-syn and Aβ42 oligomerization and fibrillogenesis[2]. Tolcapone induces oxidative stress leading toapoptosisand inhibition of tumor growth in neuroblastoma[3].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

分子量

277.27

Formula

C14H7D4NO5

CAS 号

1246816-93-2

中文名称

托卡朋 d4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.