1. Cell Cycle/DNA Damage Vitamin D Related/Nuclear Receptor Metabolic Enzyme/Protease
  2. PPAR
  3. Leriglitazone

Leriglitazone  (Synonyms: MIN-102; Hydroxypioglitazone)

目录号: HY-117727
产品使用指南

Leriglitazone (MIN-102; Hydroxypioglitazone),吡格列酮的代谢产物。Leriglitazone 是 PPARγ 激动剂,通过稳定 PPARγ (AF-2) 共激活剂结合表面和增强共激活剂结合能力,提供高转录效力。Leriglitazone 与 PPARγC (LBD) 结合,其 Ki 值为 1.2 μM,诱导 PPARγ (LBD) 转录效率,EC50 为 680 nM。

在相同的摩尔浓度下,化合物盐形式与游离形式有相同的生物活性,但盐形式 Leriglitazone hydrochloride 通常具有更好的水溶性和稳定性。

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Leriglitazone Chemical Structure

Leriglitazone Chemical Structure

CAS No. : 146062-44-4

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Leriglitazone 的其他形式现货产品:

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  • 参考文献

生物活性

Leriglitazone (MIN-102; Hydroxypioglitazone), a metabolite of pioglitazone. Leriglitazone PioOH is a PPARγ agonist, stabilizes the PPARγ activation function-2 (AF-2) co-activator binding surface and enhances co-activator binding, affording slightly better transcriptional efficacy. Leriglitazone binds to the PPARγ C-terminal ligand-binding domain (LBD) with a Ki of 1.2 μM,Leriglitazone induces transcriptional efficacy of the PPARγ (LBD) with an EC50 of 680 nM[1].

IC50 & Target

Ki: 1.2 μM (PPARγ LBD); EC: 680 nM (PPARγ LBD) (Leriglitazone)[1]

Clinical Trial
分子量

372.44

Formula

C19H20N2O4S

CAS 号
性状

固体

颜色

Off-white to light yellow

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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HY-117727
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