Saikogenin D 皂苷元 D,98.95%

产品编号:Bellancom-N4237| CAS NO:5573-16-0| 分子式:C30H48O4| 分子量:472.70

Saikogenin D 分离自 Bupleurum chinense ,具有抗炎作用。Saikogenin D 激活环氧合酶,将花生四烯酸转化为环氧二十烷酸和二羟基二十碳三烯酸,其代谢产物继而抑制前列腺素E2 (PGE2) 的产生。 由于细胞内 Ca2+ 的释放,Saikogenin D 导致 [Ca2+]i 升高。

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-N4237
1400.00 杭州 北京(现货)
Bellancom-N4237
2900.00 杭州 北京(现货)

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Saikogenin D 皂苷元 D

产品介绍 Saikogenin D 分离自 Bupleurum chinense ,具有抗炎作用。Saikogenin D 激活环氧合酶,将花生四烯酸转化为环氧二十烷酸和二羟基二十碳三烯酸,其代谢产物继而抑制前列腺素E2(PGE2)的产生。 由于细胞内 Ca2+ 的释放,Saikogenin D导致 [Ca2+]i 升高。
生物活性

Saikogenin D is isolated from Bupleurum chinense, has anti-inflammatory effects. Saikogenin D activates epoxygenases that converts arachidonic acid to epoxyeicosanoids and dihydroxyeicosatrienoic acids, and the metabolites secondarily inhibit prostaglandin E2 (PGE2) production. Saikogenin D results in an elevation of [Ca2+]i due to Ca2+ release from intracellular stores.

体外研究

Saikogenin D (1-20 μM) inhibits PGE2 production induced by the Ca2+ ionophore A23187 in a concentration-dependent manner with an IC50 value of 3 μM in C6 rat glioma cells.
Saikogenin D (10-100 μM) elevates [Ca2+]i in a concentration-dependent manner with a EC50 value of 35 μM in the presence or absence of extracellular Ca2+ in C6 rat glioma cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
体内研究
性状Solid
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

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