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 |
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| 10MG | ¥648 | 有现货 |
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| 25MG | ¥1320 | 有现货 |
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| 50MG | ¥2001 | 有现货 |
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| 100MG | ¥3013 | 有现货 |
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| 200MG | ¥4447 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称Indeglitazar
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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
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产品简述Indeglitazar 是口服的 PPAR 全激动剂(PPAR 亚型 α (α)、δ (δ) 和 gamma (γ))。
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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.
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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.
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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.
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同义词PPM 204
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通路Metabolic Enzyme/Protease
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靶点PPAR
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受体ABCG2| Antibacterial| Antibiotic| BCRP
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研究领域——
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适应症——
化学信息
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CAS Number835619-41-5
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分子量389.42
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分子式C19H19NO6S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (256.79 mM)
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SMILESO=C(O)CCC1=CN(C=2C=CC(OC)=CC21)S(=O)(=O)C3=CC=C(OC)C=C3
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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.
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