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- 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:
Panaxoside Rf
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
52286-58-5
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1498.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥453.0 |
| 规格: | 5 mg | 产品价格: | ¥990.0 |
| 规格: | 10 mg | 产品价格: | ¥1700.0 |
| 规格: | 25 mg | 产品价格: | ¥3400.0 |
| 规格: | 50 mg | 产品价格: | ¥5400.0 |
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Ginsenoside Rf
CAS No. : 52286-58-5
MCE 国际站:Ginsenoside Rf
产品活性:Ginsenoside Rf 是人参根的一种微量成分。 Ginsenoside Rf 抑制 N 型 Ca2+ 通道。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling | Metabolic Enzyme/Protease
作用靶点:Calcium Channel | Endogenous Metabolite
In Vitro: Ginsenoside Rf is a saponin, which is present in only trace amounts within ginseng. At saturating concentrations, Ginsenoside Rf rapidly and reversibly inhibits N-type, and other high-threshold, Ca2+ channels in rat sensory neurons to the same degree as a maximal dose of opioids. The effect is dose-dependent (half-maximal inhibition: 40 μM) and it is virtually eliminated by pretreatment of the neurons with pertussis toxin, an inhibitor of G(o) and Gi GTP-binding proteins. Ginsenoside Rf also inhibits Ca2+ channels in the hybrid F-11 cell line.
In Vivo: Since inhibition of Ca2+ channels in sensory neurons contributes to antinociception by opioids, analgesic actions of Ginsenoside Rf are tested. Dose-dependent antinociception is found by systemic administration of Ginsenoside Rf in mice using two separate assays of tonic pain: in the acetic acid abdominal constriction test, the ED50 is 56±9 mg/kg, a concentration similar to those reported for aspirin and acetaminophen in the same assay; in the tonic phase of the biphasic formalin test, the ED50 is 129±32 mg/kg.
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