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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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。 |
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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) |
参考文献 |
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