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- 2025年07月03日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名：
Gentiopicrin
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
20831-76-9
- 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： | ￥770.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥218.0 |
| 规格： | 5 mg | 产品价格： | ￥437.0 |
| 规格： | 10 mg | 产品价格： | ￥700.0 |
| 规格： | 25 mg | 产品价格： | ￥1400.0 |
| 规格： | 50 mg | 产品价格： | ￥2400.0 |
| 规格： | 100 mg | 产品价格： | ￥3700.0 |
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Gentiopicroside
CAS No. : 20831-76-9
MCE 国际站：Gentiopicroside
产品活性：Gentiopicroside 是一种天然的环烯醚萜苷，能够抑制 P450 的活性，对 CYP2A6 的 IC50 和 Ki 值分别为 61 µM 和 22.8 µM；Gentiopicroside 具有抗炎和抗氧化活性。
研究领域：Metabolic Enzyme/Protease | Anti-infection
作用靶点：Cytochrome P450 | HCV
In Vitro: Gentiopicroside inhibits P450 activity, with an IC50 and a Ki of 61 µM and 8.12 µM for CYP2A6, also slightly inhibits CYP2E1 activity with an IC50 of 1.6 mM, but shows no inhibition on CYP1A2 and CYP3A4. Gentiopicroside (12.5, 25 and 50 μM) inhibits RANKL-induced osteoclast formation from mouse bone marrow macrophages (BMMs) in a dose-dependent manner, blocks the expression of osteoclast-related proteins, prevents receptor activator of nuclear factor-κB ligand (RANKL)-triggered JNK and NF-κB activation. Gentiopicroside (50 μM) also inhibits RANKL-induced bone resorption.
In Vivo: Gentiopicroside (20, 40, and 80 mg/kg, p.o.) significantly reduces gastric ulcerindex in mice. Gentiopicroside (20, 40, and 80 mg/kg) also ovbiously decreases the levels of HSP-70, TNF-α, IL-6, MDA and increases ncreased GSH level and SOD activity. In addition, Gentiopicroside normalizes EGF and VEGF level in mice.
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文献和实验of Gentiopicroside in Xiedan Pill by TLCS ZH0NG Qiang，XIE Jiao，PAN Hong Abstract：Objective：To determine the contents of gentiopicroside in Xiedan Pill by TLCS．Methods：The dual wavelength reflection zigzag scanning was employed in this determination
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