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刺五加苷E
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| 中文名 |
刺五加甙 E |
|---|---|
| 英文名 |
Eleutheroside E |
| 中文别名 |
刺五加甙E | 刺五加苷E,五加苷E | 刺五加苷E | 刺五加苷E | 五加苷E | 刺五加苷 E | 刺五加甙 |
| 英文别名 |
更多 |
| 描述 |
刺五加苷E (Eleutheroside E)是刺五加的重要成分，具有抗炎，保护缺血心脏的作用。 |
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| 相关类别 |
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| 溶解度 |
体外：
DMSO：≥7.5mg / mL（10.10 mM） * “≥”表示可溶，但饱和度未知。
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| 储备液 |
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| 存储 |
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| 运输 |
室温;可能会有所不同 |
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| SMILES |
COC(C=C1[C@H]2[C@@](CO[C@@H]3C4=CC(OC)=C(O[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5CO)C(OC)=C4)([H])[C@]3([H])CO2)=C(C(OC)=C1)O[C@@H]([C@@H]([C@@H](O)[C@@H]6O)O)O[C@@H]6CO |
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| 参考文献 |
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| 相关活性 小分子 |
磺丁醚-beta-环糊精 | 环孢菌素 | 2,7-二氯二氢代荧光黄二醋酸 | 1-甲基-4-苯基-1,2,3,6-四氢吡啶盐酸盐 | 4′,4”-双-2-咪唑啉-2-基对苯二丙烯酰苯胺二盐酸盐 | 乙莫克舍 | TD139 | Mitoquinone甲磺酸盐 | GSK2795039 | 5,5’,6,6’-四氯-1,1’,3,3’-四乙基苯并咪唑羰花青碘化物 | 胞内钙荧光探针 BAPTA-AM | AP20187 | GKT137831 | D-虫荧光素游离酸 | 野百合碱 |
| 密度 | 1.5±0.1 g/cm3 |
|---|---|
| 沸点 | 935.7±65.0 °C at 760 mmHg |
| 熔点 | 255 – 260?C |
| 分子式 | C34H46O18 |
| 分子量 | 742.718 |
| 闪点 | 519.7±34.3 °C |
| 精确质量 | 742.268433 |
| PSA | 254.14000 |
| LogP | -3.91 |
| 外观性状 | 无色微结晶粉末 |
| 蒸汽压 | 0.0±0.3 mmHg at 25°C |
| 折射率 | 1.616 |
| 储存条件 | 2-8°C |
| 符号 |
GHS07 |
|---|---|
| 信号词 |
Warning |
| 危害声明 |
H302 |
| 危害码 (欧洲) |
Xn |
| 风险声明 (欧洲) |
22 |
| 安全声明 (欧洲) |
24/25 |
| 危险品运输编码 | NONH for all modes of transport |
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[Studies on chemical constituents from stem barks of Fraxinus paxiana]. Zhongguo Zhong Yao Za Zhi 33(16) , 1990-3, (2008)
To investigate the chemical constituents of Fraxinus paxiana.The chemical constituents were isolated and purified by chromatographic techniques and the structures of the compounds were identified with…
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[Chemical constituents from flowers of Chrysanthemum indicum]. Zhongguo Zhong Yao Za Zhi 35(6) , 718-21, (2010)
To investigate the chemical constituents of the flowers of Chrysanthemum indicum.The chemical constituents were isolated by various column chromatographic methods. The structures were identified by sp…
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[Studies on phenylpropanoids from herbs of Eriophyton wallichii]. Zhongguo Zhong Yao Za Zhi 33(22) , 2636-9, (2008)
To study the chemical constituents of Eriophyton wallichii.Compounds were separated and purified by column chromatographic methods, and their structures were elucidated by spectroscopic methods.Eight …
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4-{(1R,3aR,4S,6aS)-4-[4-(β-L-Glucopyranosyloxy)-3,5-dimethoxyphenyl]tetrahydro-1H,3H-furo[3,4-c]furan-1-yl}-2,6-dimethoxyphenyl β-D-glucopyranoside |
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β-D-Glucopyranoside, 4-[(1R,3aR,4S,6aS)-4-[4-(β-L-glucopyranosyloxy)-3,5-dimethoxyphenyl]tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenyl |
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β-D-Glucopyranoside, 4-[(1R,3aS,4S,6aR)-4-[4-(β-L-glucopyranosyloxy)-3,5-dimethoxyphenyl]tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2,6-dimethoxyphenyl |
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(2R,3S,4R,5R,6S)-2-[4-[6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
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4-{(1R,3aS,4S,6aR)-4-[4-(β-L-Glucopyranosyloxy)-3,5-dimethoxyphenyl]tetrahydro-1H,3H-furo[3,4-c]furan-1-yl}-2,6-dimethoxyphenyl β-D-glucopyranoside |
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