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5-Fluorouracil-d1
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。
5-Fluorouracil-d1图片
CAS NO:90344-84-6
包装与价格:
包装价格(元)
5mg电议
50mg电议

产品名称
5-FU-d1
产品介绍
5-Fluorouracil-d1 (5-FU-d1) 是 5-Fluorouracil 的氘代物。5-Fluorouracil (5-FU) 是一种尿嘧啶的类似物 (nucleoside antimetabolite/analog),是一种有效的抗肿瘤药。5-Fluorouracil 通过抑制胸苷酸合成酶影响嘧啶的合成,从而耗尽细胞内dTTP 池。5-Fluorouracil 诱导细胞凋亡 (apoptosis),可用作化学敏化剂。5-Fluorouracil 还可抑制HIV病毒。5-Fluorouracil (5-FU) 可破坏外泌体特异性的 rRNA。
生物活性

5-Fluorouracil-d1 (5-FU-d1) is the deuterium labeled 5-Fluorouracil. 5-Fluorouracil (5-FU) is an analogue of uracil and a potent antitumor agent. 5-Fluorouracil affectspyrimidine synthesisby inhibiting thymidylate synthetase thus depleting intracellular dTTP pools. 5-Fluorouracil inducesapoptosisand can be used as a chemical sensitizer[1][2]. 5-Fluorouracil also inhibitsHIV[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

131.08

Formula

C4H2DFN2O2

CAS 号

90344-84-6

中文名称

5-氟脲嘧啶 d1

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.