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  2. PPAR
  3. PPARγ agonist-22

PPARγ agonist-22 是一种 PPARγ 激动剂。PPARγ agonist-22 可促进细胞对葡萄糖的摄取。PPARγ agonist-22 可减少脂肪细胞中的脂质积累。PPARγ agonist-22 可用于 2 型糖尿病的研究。

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PPARγ agonist-22

PPARγ agonist-22 Chemical Structure

CAS No. : 931956-54-6

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生物活性

PPARγ agonist-22 is a PPARγ agonist. PPARγ agonist-22 promotes cellular glucose uptake. PPARγ agonist-22 reduces lipid accumulation in adipocytes. PPARγ agonist-22 can be used in the research of type 2 diabetes[1].

IC50 & Target[1]

PPAR-γ

 

体外研究
(In Vitro)

PPARγ agonist-22 (Compound Sn8) (12.5-200 μg/mL;24 h) 在低浓度下对 3T3-L1 前脂肪细胞和 C2C12 成肌细胞无细胞毒性,但高浓度下会诱导浓度依赖性的细胞毒性[1]
PPARγ agonist-22 (25 μg/mL;8 days) 在 3T3-L1 前脂肪细胞中展现出抗成脂活性,可将分化 8 天后的脂质积累量降至对照组水平的 61.03%[1]
PPARγ agonist-22 (100 μg/mL; 24 h) 显著提高 C2C12 成肌细胞的葡萄糖摄取量[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

465.57

Formula

C27H23N5OS

CAS 号
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.

纯度 & 产品资料
参考文献
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Help & FAQs
  • 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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产品名称:
PPARγ agonist-22
目录号:
HY-181233
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