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(3beta)-3-{[6-Deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->4)]-alpha-L-arabinopyranosyl]oxy}-23-hydroxyolean-12-en-28-oic acid(CAS: 68027-15-6)
![(3beta)-3-{[6-Deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->4)]-alpha-L-arabinopyranosyl]oxy}-23-hydroxyolean-12-en-28-oic acid](https://cnstatic.chemtradehub.com/structs/680/68027-15-6-43a9.webp "(3beta)-3-{[6-Deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->4)]-alpha-L-arabinopyranosyl]oxy}-23-hydroxyolean-12-en-28-oic acid")
CAS号
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基本信息
分子式
C47H76O17
分子量
913.11 g/mol
Physical Properties
熔点
239-241 ºC
密度
1.40±0.1 g/cm3 (20 ºC 760 Torr),
化学标识符
SMILES
CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)OC8C(C(C(C(O8)CO)O)O)O)O)O)O)O
InChIKey
SOLICHUQXFAOEP-YDIXZRNLSA-N
数据库引用
MDL号
MFCD28124361
常见问题
白头翁皂苷D是一种复杂的三萜皂苷，具有显著的结晶形态。其分子量约为1243.48 Da。在水中溶解度较低，在有机溶剂如乙醇、甲醇中具有较好的溶解性。该化合物在酸性和碱性条件下都表现出一定的反应活性，但在中性条件下相对稳定。
白头翁皂苷D的合成通常采用半合成方法，首先从白头翁中提取天然化合物，然后通过化学修饰获得目标化合物。常见的合成方法包括糖苷键的裂解和重新糖基化，使用催化剂如硫酸或甲醇钠。该过程的产率约为60-70%，选择性良好。
白头翁皂苷D因其生物活性，在医药行业中有着广泛的应用，主要用于抗炎、抗肿瘤和免疫调节等领域。此外，它还被用于化妆品行业，作为天然活性成分，改善皮肤健康和抗衰老效果。
在处理白头翁皂苷D时，应佩戴个人防护装备，如手套、护目镜和实验室外套。操作应在通风橱中进行，以减少吸入风险。如果发生泄露，应立即将污染区域隔离，并使用适当的吸附材料进行清理。处理完毕后，参考安全数据表(SDS)对废弃物进行妥善处理。
安全须知
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