黑海常春藤苷A1
| 中文名称 | 黑海常春藤苷A1 |
|---|---|
| 中文同义词 | HEDERACOLCHISIDE A1(标准品);黑海常春藤苷A1;革叶常春藤皂苷A1;竹节香附皂苷R13;齐墩果酸-3-O-Α-L鼠李吡喃糖基-(1→2)[Β-D-葡萄吡喃糖基-(1→4)] -Α-L-吡喃阿拉伯糖苷;黑海常春藤皂苷A1;齐墩果酸-3-O-Β-D-吡喃鼠李糖基-(1→2)-[Β-D-吡喃葡萄糖基-(1→4)]-Α-L-吡喃阿拉伯糖苷;齐墩果酸-3-O-Β-D-吡喃鼠李糖基-(1→2)-Β-D-吡喃葡萄糖基-(1→4)-Α-L-吡喃阿拉伯糖苷 |
| 英文名称 | Hederacolchiside A1 |
| 英文同义词 | Hederacolchiside A1;HEDERACOLCHISIDE A1;;Raddeanoside R13;Olean-12-en-28-oicacid, 3-[(O-6-deoxy-a-L-mannopyranosyl-(12)-O-[b-D-glucopyranosyl-(14)]-a-L-arabinopyranosyl)oxy]-, (3b)-;Oleanolic acid-3-O-β-D-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→4)-]-α-L-arabinopyranoside，Hederacolchiside A1;Olean-12-en-28-oic acid, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]-, (3β)-;Hederacolchiside A1 USP/EP/BP;Oleanolic acid-3-O-β-D-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)--α-L-arabinopyranoside，Hederacolchiside A1 |
| CAS号 | 106577-39-3 |
| 分子式 | C47H76O16 |
| 分子量 | 897.1 |
| EINECS号 | |
| 相关类别 | 植物提取物;标准品;中药对照品;标准品-中药标准品;对照品;三萜;标准品 -中药标准品;标准品，对照品;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;reagent;standard substance;Triterpenoids |
| Mol文件 | 106577-39-3.mol |
| 结构式 |  |
黑海常春藤苷A1 性质
| 熔点 | 253-255℃ (methanol , water ) |
|---|---|
| 沸点 | 967.2±65.0 °C(Predicted) |
| 密度 | 1.36±0.1 g/cm3 (20 ºC 760 Torr) |
| 储存条件 | 4°C, protect from light |
| 溶解度 | 溶于二甲基亚砜 |
| 酸度系数(pKa) | 4?+-.0.70(Predicted) |
Hederacolchiside A1 是从白头翁中分离的，通过调节 PI3K/Akt/mTOR 信号通路诱导凋亡，从而抑制肿瘤细胞的增殖。Hederacolchiside A1 具有抗血吸虫病活性，影响体内和体外的寄生虫生存力。
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PI3K
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Akt
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mTOR
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Hederacolchiside A1 reduces the mitochondrial membrane potential and Bcl-2 protein levels, whereas cleaved caspase-3 was higher.
Hederacolchiside A1 effectively inhibits the phosphorylations of phosphatidylinositol 3 kinase (PI3K), protein kinase B (Akt), and mammalian target of rapamycin (mTOR) .
hederacolchiside A1 (3.0, 4.5, and 6.0 mg/kg, ip) can significantly inhibit the weight of tumor in an H22 xenograft model.
Hederacolchiside A1 (3.25, 7.5, and 15.0 mg/kg, ig) can significantly inhibit the weight of tumor in nude mice xenograft tumor models using human breast carcinoma MCF-7 cells.
安全信息
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2024/01/25 | HY-N6950 | Hederacolchiside A1 | 1 mg | 600元 | |
| 2024/01/25 | HY-N6950 | 黑海常春藤苷A1 Hederacolchiside A1 | 106577-39-3 | 5mg | 2020元 |