天然产物 糖类和糖苷 Saccharides and Glycosides
Poliumoside (Synonyms: 金石蚕苷) 纯度: 99.80%
Poliumoside,是一种从 Brandisia hancei 的茎和叶中分离出来的咖啡酰化的苯丙烷糖苷。Poliumoside 可以抑制晚期糖基化终产物 (AGE) 的形成和大鼠晶状体醛糖还原酶 (RLAR) ,IC50 值分别为 19.69 和 8.47 μM。Poliumoside 还具有抗炎和抗氧化活性。
![Poliumoside Chemical Structure Poliumoside(Synonyms: 金石蚕苷)](http://www.boykyo.com.cn/wp-content/uploads/2022/05/hy-n0033.gif)
Poliumoside Chemical Structure
CAS No. : 94079-81-9
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥1841 | In-stock | |
10 mg | ¥1674 | In-stock | |
50 mg | ¥5189 | In-stock | |
100 mg | ¥8296 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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Poliumoside 相关产品
•相关化合物库:
- Natural Product Library Plus
- Bioactive Compound Library Plus
- Immunology/Inflammation Compound Library
- Metabolism/Protease Compound Library
- Natural Product Library
- Anti-Cardiovascular Disease Compound Library
- Phenols Library
- Traditional Chinese Medicine Monomer Library
- Glucose Metabolism Compound Library
- Targeted Diversity Library
生物活性 |
Poliumoside, a caffeoylated phenylpropanoid glycoside, is isolated from Brandisia hancei stems and leaves. Poliumoside is an advanced glycation end product (AGE) formation and rat lens aldose reductase (RLAR) inhibitor, with IC50s of 19.69 and 8.47 μM, respectively. Poliumoside also has antiinflammatory and antioxidant activity[1][2][3]. |
IC50 & Target |
IC50: 8.47 μM (aldose reductase)[1] |
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体外研究 (In Vitro) |
Poliumoside inhibits AGE formation and RLAR, with IC50s of 19.69, and 8.47 μM, respectively[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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体内研究 (In Vivo) |
Poliumoside inhibits vessel dilation in larval zebrafish[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
770.73 |
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Formula |
C35H46O19 |
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CAS 号 |
94079-81-9 |
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中文名称 |
金石蚕苷;金石蚕甙 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (129.75 mM; Need ultrasonic) Ethanol : 50 mg/mL (64.87 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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