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Indeglitazar

CAS No. 835619-41-5

Indeglitazar ( PPM 204 )

产品货号. M26716 CAS No. 835619-41-5

Indeglitazar 是口服的 PPAR 全激动剂(PPAR 亚型 α (α)、δ (δ) 和 gamma (γ))。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥518 有现货
10MG ¥648 有现货
25MG ¥1320 有现货
50MG ¥2001 有现货
100MG ¥3013 有现货
200MG ¥4447 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Indeglitazar
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Indeglitazar 是口服的 PPAR 全激动剂(PPAR 亚型 α (α)、δ (δ) 和 gamma (γ))。
  • 产品描述
    Indeglitazar is orally available pan-agonist of PPAR (PPAR subtypes alpha (α), delta (δ), and gamma (γ)).(In Vitro):Measuring in part functional insulin sensitization capability of the cells, Indeglitazar shows an EC50 of 0.32 μM compared with Rosiglitazone, which shows an EC50 of 13 nM, in an assay of preadipocyte differentiation.(In Vivo):In Zucker rat model of diabetes, Indeglitazar (10 mg/kg; i.v.) significantly lowers the levels of glucose, HbA1C, triglycerides. In the ob/ob model of diabetes and insulin resistance, Indeglitazar significantly decreases glucose, insulin, triglycerides, and free fatty acid levels. The level of Adiponectin (day 21) is essentially unchanged, thus the observed reductions in glucose and HbA1C are achieved in an adiponectin-independent fashion.
  • 体外实验
    In an assay of preadipocyte differentiation, measuring in part functional insulin sensitization capability of the cells, Indeglitazar shows an EC50 of 0.32 μM compared with Rosiglitazone, which shows an EC50 of 13 nM, although the maximal response obtained from the 2 compounds is comparable.
  • 体内实验
    An initial assessment of in vivo activity is carried out using the Zucker rat model of diabetes. The significant lowering of glucose, HbA1C, triglycerides, and total cholesterol are observed after i.v. treatment with 10 mg/kg Indeglitazar once per day for 3 weeks. Notably, the level of Adiponectin (on day 21) is essentially unchanged in treated vs. untreated animals (4.8 mcg/mL vs. 4.9 mcg/mL), thus the observed reductions in glucose and HbA1C are achieved in an adiponectin-independent fashion. These differences in the effects of Indeglitazar in vivo may be a consequence of synergy between the 3 PPAR activities or because of the SPPARM profile of the compound, or a combination of these factors. The oral activity of Indeglitazar is assessed in the ob/ob model of diabetes and insulin resistance. Indeglitazar significantly decreases glucose, insulin, triglycerides, and free fatty acid levels.
  • 同义词
    PPM 204
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    PPAR
  • 受体
    ABCG2| Antibacterial| Antibiotic| BCRP
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    835619-41-5
  • 分子量
    389.42
  • 分子式
    C19H19NO6S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (256.79 mM)
  • SMILES
    O=C(O)CCC1=CN(C=2C=CC(OC)=CC21)S(=O)(=O)C3=CC=C(OC)C=C3
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Rabindran SK, et al. Fumitremorgin C reverses multidrug resistance in cells transfected with the breast cancer resistance protein. Cancer Res. 2000 Jan 1;60(1):47-50.
产品手册
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