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Montelukast-d6
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。
Montelukast-d6图片
规格:98%
分子量:592.22
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议

产品介绍
Montelukast-d6 (MK0476-d6 free acid) 是 Montelukast 的氘代物。Montelukast sodium 是一种有效的、选择性和具有口服活性的半胱氨酸白三烯受体 1 (Cysltr1) 拮抗剂。Montelukast sodium 可用于研究预防哮喘和肝损伤。Montelukast sodium 在肠缺血-再灌注损伤中也具有抗氧化作用,还可以减少心脏损伤。
货号:ajcx35402
CAS:1093746-29-2
分子式:C35H30D6ClNO3S
分子量:592.22
溶解度:N/A
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Montelukast-d6 (MK0476-d6 free acid) is the deuterium labeled Montelukast (sodium). Montelukast sodium is a potent, selective and orally active antagonist of cysteinyl leukotriene receptor 1 (Cysltr1). Montelukast sodium can be used for the reseach of asthma and liver injury. Montelukast sodium also has an antioxidant effect in intestinal ischemia-reperfusion injury, and could reduce cardiac damage[1].

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].

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Pu S, et, al. Montelukast Prevents Mice Against Acetaminophen-Induced Liver Injury. Front Pharmacol. 2019 Sep 18; 10:1070.;William RHJ, et, al. A role for cysteinyl leukotrienes in airway remodeling in a mouse asthma model. Am J Respir Crit Care Med. 2002 Jan 1; 165(1): 108-16.