匹格列酮盐酸盐 T0214L

Product Introduction
Bioactivity


英文名: Pioglitazone hydrochloride

描述: Pioglitazone hydrochloride (AD 4833) 是一种选择性PPARγ激动剂，高亲和力结合到 PPARγ 配体结合域。作用于人和鼠 PPARγ，EC50分别为 0.93 和 0.99 μM。它是一种口服活性噻唑烷二酮的盐酸盐，具有抗糖尿病特性和潜在的抗肿瘤活性。

细胞实验: In order to evaluate cell proliferation, HIT-T15 cells are seeded on 96-well plates (3×104 cells/well) and cultured for 5 days as described. Viable cells are determined using the Cell Titer 96 Aqueous One Solution Cell Proliferation Assay. To evaluate cell apoptosis and cell necrosis, HIT-T15 cells are plated on 6-well dishes (7×105 cells/well) for 5 days in standard conditions (CTR) or in the presence of AGEs (AGEs) with or without Pioglitazone (0.5 or 1 μM) or AG (1 mM). They are then processed to measure both the activity of caspase-3 and the activity of lactate dehydrogenase (LDH) (a stable cytosolic enzyme that is a marker of cell membrane damage and cell death due to necrosis) using Cytotox 96 Non Radioactive Cytotoxicity Assay[2].

体外活性: 在雄性肥胖鼠中,口服 Pioglitazone（0.3-3 mg/kg）7天,能够以剂量依赖性的方式地降低高血糖症,高脂血症,和高胰岛素血症.

体内活性: Pioglitazone 通过抑制iNOS的表达和NO的产生,保护多巴胺能神经元被LPS损伤。Pioglitazone也能够抑制脂多糖诱导的p38蛋白磷酸化。

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: DMSO : 50 mg/mL (127.26 mM)


关键字: Pioglitazone hydrochloride | PPAR | Ferroptosis | Inhibitor | Pioglitazone | inhibit | AD-4833 | Pioglitazone Hydrochloride | Peroxisome proliferator-activated receptors | AD4833

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相关库: Anti-Aging Compound Library | FDA-Approved Drug Library | Drug Repurposing Compound Library | Hematopoietic Toxicity Compound Library | Anti-Breast Cancer Compound Library | Anti-Cancer Drug Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Active Compound Library | Anti-Cancer Approved Drug Library | EMA Approved Drug Library

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