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  3. Pioglitazone potassium

Pioglitazone potassium  (Synonyms: U 72107 potassium)

目录号: HY-13956B
产品使用指南

Pioglitazone (U 72107) potassium 是一种具有口服活性的选择性 PPARγ (peroxisome proliferator-activated receptor) 激动剂,高亲和力结合到 PPARγ 配体结合域,作用于人和鼠 PPARγEC50 分别为 0.93 μM 和 0.99 μM。Pioglitazone potassium 可用于糖尿病研究。

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Pioglitazone potassium Chemical Structure

Pioglitazone potassium Chemical Structure

CAS No. : 1266523-09-4

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Pioglitazone potassium 的其他形式现货产品:

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Pioglitazone (U 72107) potassium is an orally active and selective PPARγ (peroxisome proliferator-activated receptor) agonist with high affinity binding to the PPARγ ligand-binding domain with EC50 of 0.93 μM and 0.99 μM for human and mouse PPARγ, respectively. Pioglitazone potassium can be used in diabetes research[2][3][4].

IC50 & Target[1]

mouse PPARγ

0.99 μM (EC50)

h-PPARγ

0.93 μM (EC50)

hPPARδ

43 μM (EC50)

hPPARα

100 μM (EC50)

mouse PPARα

100 μM (EC50)

体外研究
(In Vitro)

Pioglitazone potassium (0.5 or 1 μM, 5 days) can completely prevent AGEs (advanced glycation end-products)-induced β-cell necrosis and the increase of caspase-3 thereby avoiding the impaired viability caused by AGEs in pancreatic beta cell line HIT-T15[2].
Pioglitazone potassium (1 μM, 1 h) can stimulate insulin secretion induced by low glucose concentration and attenuate the GSSG/GSH ratio in cells cultured with AGEs[2].

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

体内研究
(In Vivo)

Pioglitazone potassium (oral gavage, 10 or 30 mg/kg, once daily, 14 days) can induce improvements in insulin resistance and diabetes that may be lipocalin-dependent in the liver but not in skeletal muscle[3].
Pioglitazone potassium (oral gavage, 10 mg/kg, once daily, 4 weeks) can significantly reduce body weight (BW), cardiac hypertrophy, elevated blood glucose levels and improve the associated dyslipidemia[4].

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

Animal Model: ob/ob and adipo-/- ob/ob mice with a C57Bl/6 background[3]
Dosage: 10 or 30 mg/kg
Administration: Oral gavage; once daily; 14 days
Result: Showed no changes of serum-free fatty acid and triglyceride levels as well as adipocyte sizes in ob/ob and adipo-/- ob/ob C57BL/6 mice at 10 mg/kg but significantly reduced to a similar degree at 30 mg/kg.
Also showed no changes of expressions of TNFα and resistin in adipose tissues of ob/ob and adipo-/- ob/ob mice at 10 mg/kg but decreased at 30 mg/kg.
Animal Model: Male Wistar albino rats[4]
Dosage: 10 mg/kg
Administration: Oral gavage; once daily; 4 weeks
Result: Decreased the elevated serum levels of both creatinine and creatine kinase-MB (CK-MB), TGF-β1 gene expression and regulated the expression of MMP-2/TIMP-2 system.
Clinical Trial
分子量

394.53

Formula

C19H19KN2O3S

CAS 号
中文名称

吡格列酮钾盐;酮基匹格列酮钾盐

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
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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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Pioglitazone potassium
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HY-13956B
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