中文名 | 淫羊藿次甙E5 |
英文名 | Icariside E5 |
别名 | 淫羊藿次甙E5 淫羊藿次甙 E5 |
英文别名 | Icariside E5 3-[4-β-D-Glucopyranosyloxy-5-methoxy-3-[2-(4-hydroxy-3-methoxyphenyl)-1-(hydroxymethyl)ethyl]phenyl]-2-propen-1-ol b-D-Glucopyranoside,2-[(1R)-2-hydroxy-1-[(4-hydroxy-3-methoxyphenyl)methyl]ethyl]-4-[(1E)-3-hydroxy-1-propen-1-yl]-6-methoxyphenyl β-D-Glucopyranoside, 2-[(1R)-2-hydroxy-1-[(4-hydroxy-3-methoxyphenyl)methyl]ethyl]-4-[(1E)-3-hydroxy-1-propen-1-yl]-6-methoxyphenyl |
CAS | 126176-79-2 |
化学式 | C26H34O11 |
分子量 | 522.54 |
密度 | 1.413±0.06 g/cm3(Predicted) |
沸点 | 807.6±65.0 °C(Predicted) |
比旋光度 | -118.8 (c, 1.04 in MeOH) |
酸度系数 | 10.09±0.20(Predicted) |
存储条件 | 2-8℃ |
外观 | 粉末 |
MDL号 | MFCD17214940 |
体外研究 | Icariside E5 (5, 10, 20, 40 µM; for 48 h) slightly promotes the proliferation of human umbilical vein endothelial cells (HUVECs). Icariside E5 does not have the pharmacological effect of scavenging ROS. Icariside E neither induces an increase in the intracellular levels of reactive oxygen species nor affects the mitochondria permeability transition, and it does not signal through the vanilloid receptor type 1. It protects Jurkat cells from apoptosis induced by the oxidative stress mediated by serum withdrawal. |
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