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Fmoc-leucine-d3
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。
Fmoc-leucine-d3图片
CAS NO:538372-74-6
包装与价格:
包装价格(元)
1mg电议
5mg电议

产品名称
N-FMOC-leucine-d3
NPC 15199-d3
NSC 334290-d3
产品介绍
Fmoc-leucine-d3 是 Fmoc-leucine 氘代物。Fmoc-leucine 是一种选择性的PPARγ调节剂。与罗格列酮相比,Fmoc-leucine 激活 PPARγ 的效力较低,但最大效应相似。Fmoc-leucine 改善正常、饮食诱导的葡萄糖不耐受和糖尿病 db/db 小鼠的胰岛素敏感性。Fmoc-leucine 具有较低的诱导脂肪生成活性。
生物活性

Fmoc-leucine-d3 is the deuterium labeled Fmoc-leucine. Fmoc-leucine is a selectivePPARγ modulator. Fmoc-leucine activatesPPARγwith a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improvesinsulinsensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity[1].

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

356.43

Formula

C21H20D3NO4

CAS 号

538372-74-6

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.