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- 详细信息
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture
- 英文名:
Setogepram sodium; PBI-4050 sodium
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1254472-97-3
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1130.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥450.0 |
| 规格: | 5 mg | 产品价格: | ¥1040.0 |
| 规格: | 10 mg | 产品价格: | ¥1690.0 |
| 规格: | 25 mg | 产品价格: | ¥2880.0 |
| 规格: | 50 mg | 产品价格: | ¥4120.0 |
| 规格: | 100 mg | 产品价格: | ¥5725.0 |
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Fezagepras sodium
CAS No. : 1254472-97-3
MCE 国际站:Fezagepras sodium
产品活性:Fezagepras (Setogepram) sodium 是一种具有口服活性的 GPR40 激动剂和 GPR84 拮抗剂或反向激动剂。Fezagepras sodium 减轻肾,肝和胰腺纤维化。Fezagepras sodium 具有抗纤维化,抗炎和抗增殖作用。
研究领域:GPCR/G Protein
作用靶点:Free Fatty Acid Receptor | GPR84
In Vitro: Fezagepras sodium (500 μM; 24 hours) inhibits TGF-β (10 ng/mL)-activated human hepatic stellate cells (HSCs) proliferation.
Fezagepras sodium (250 or 500 μM; 24 hours) dose-dependently arrests HSCs at the G0/G1 phase without inducing apoptosis.
In Vivo: Fezagepras sodium (100 mg/kg/day; gavage from 8-20 weeks of age) markedly decreases hyperglycemia and markedly improvea glucose tolerance in type 2 diabetes eNOS-/-db/db mice.·
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