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槲皮素 3-葡糖苷 7-鼠李糖苷 | 18016-58-5

中文名称
槲皮素 3-葡糖苷 7-鼠李糖苷
中文别名
槲皮素3-葡糖苷7-鼠李糖苷;槲皮素-3-O-葡萄糖-7-O-鼠李糖苷
英文名称
quercitin-3-O-β-D-glucoside-7-O-α-L-rhamnoside
英文别名
Quercetin 3-O-Glc 7-O-Rha;quercetin 3-O-β-D-glucopyranosyl-7-O-α-L-rhamnopyranoside;quercetin 3-O-β-D-glucopyranoside-7-O-α-L-rhamnopyranoside;quercetin 3-O-glucoside-7-O-rhamnoside;quercetin 3-glucoside-7-rhamnoside;quercetin 3-O-β-glucopyranoside-7-O-α-rhamnopyranoside;Vincetoxicoside A;2-(3,4-dihydroxyphenyl)-5-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
槲皮素 3-葡糖苷 7-鼠李糖苷化学式
CAS
18016-58-5
化学式
C27H30O16
mdl
——
分子量
610.526
InChiKey
OTUCXMIQUNROBJ-JFNZIVIESA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    236℃
  • 沸点:
    999.4±65.0 °C(Predicted)
  • 密度:
    1.82±0.1 g/cm3(Predicted)
  • 溶解度:
    溶于氯仿、二氯甲烷、乙酸乙酯、DMSO、丙酮等。
  • LogP:
    1.030 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.9
  • 重原子数:
    43
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    266
  • 氢给体数:
    10
  • 氢受体数:
    16

安全信息

  • 储存条件:
    存放在2-8℃的环境中,应保持干燥并密封。

SDS

SDS:2609bd73937dff7324222b1aa4c693d6
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    槲皮素 3-葡糖苷 7-鼠李糖苷盐酸 作用下, 以 为溶剂, 反应 3.0h, 生成 L-鼠李糖葡萄糖
    参考文献:
    名称:
    Further acylated flavonol bisdesmosides fromSinocrassula indica
    摘要:
    Further investigation on the whole herbs of Sinocrassula indica (Crassulaceae) led to the isolation of four new acylated flavonol bisdesmosides, sinocrassosides A(13) (1), B-6 (2), B-7 (3), and D-4 (4), together with kaempferol 3-O--d-(6-O-acetyl)glucopyranosyl-7-O--l-rhamnopyranoside (5). Their structures were established by spectral and chemical methods.
    DOI:
    10.1080/10286020.2013.800973
  • 作为产物:
    描述:
    参考文献:
    名称:
    Further acylated flavonol bisdesmosides fromSinocrassula indica
    摘要:
    Further investigation on the whole herbs of Sinocrassula indica (Crassulaceae) led to the isolation of four new acylated flavonol bisdesmosides, sinocrassosides A(13) (1), B-6 (2), B-7 (3), and D-4 (4), together with kaempferol 3-O--d-(6-O-acetyl)glucopyranosyl-7-O--l-rhamnopyranoside (5). Their structures were established by spectral and chemical methods.
    DOI:
    10.1080/10286020.2013.800973
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文献信息

  • Flavonoids with hepatoprotective activity from the leaves of <i>Cleome viscosa</i> L.
    作者:Tan Phat Nguyen、Cong Luan Tran、Chi Hung Vuong、Thi Hong Tuoi Do、Tien Dung Le、Dinh Tri Mai、Nhat Minh Phan
    DOI:10.1080/14786419.2017.1283497
    日期:2017.11.17
    kaempferol 7-O-α-l-rhamnopyranoside (6), kaempferitrin (7) and kaempferol 3-O-β-d-glucopyranoside 7-O-α-l-rhamnopyranoside (8) were isolated by various chromatography methods from the leaves of Cleome viscosa L. Their structures were elucidated by IR, UV, HR-ESI-MS and NMR (1D & 2D) experiments. The cytotoxicity and hepatoprotective activities using HepG2 human hepatoma cell line of 1 were measured by
    一个新的黄酮醇苷命名visconoside C(1),具有七个已知黄酮醇苷一起,槲皮素-3-O-β- d吡喃葡萄糖苷7-O-α-升-rhamnopyranoside(2),槲皮素-7-O-α-升-鼠李糖吡喃糖苷(3),黄芪甲素(4),山emp酚3- O-(4- O-乙酰基)-α - l-鼠李糖吡喃糖苷(5),山emp酚7- O - α - l-鼠李糖吡喃糖苷(6),山竹铁素(7)和山奈酚3- ö - β -d吡喃葡萄糖苷7- ö - α -升-rhamnopyranoside(8)通过从所述叶片各种色谱方法分离黄花草其结构经IR,UV,HR-ESI-MS和NMR(1D&2D)阐明L.实验。通过MTT法测定使用HepG2人肝癌细胞系1的细胞毒性和保肝活性。在25μM和50μM的浓度下,1对HepG2细胞具有细胞毒性活性(与阿霉素对照相比,细胞活力分别降低至22.2和23.0%),而在100μ
  • Flavonoid glycosides from flowers of Sisymbrium officinale and Diplotaxis muralis growing in Georgia
    作者:M. D. Alaniya、N. Sh. Kavtaradze、A. V. Skhirtladze、M. G. Sutiashvili、E. P. Kemertelidze
    DOI:10.1007/s10600-012-0234-0
    日期:2012.5
  • Further acylated flavonol bisdesmosides from<i>Sinocrassula indica</i>
    作者:Hai-Hui Xie、Masayuki Yoshikawa
    DOI:10.1080/10286020.2013.800973
    日期:2013.8
    Further investigation on the whole herbs of Sinocrassula indica (Crassulaceae) led to the isolation of four new acylated flavonol bisdesmosides, sinocrassosides A(13) (1), B-6 (2), B-7 (3), and D-4 (4), together with kaempferol 3-O--d-(6-O-acetyl)glucopyranosyl-7-O--l-rhamnopyranoside (5). Their structures were established by spectral and chemical methods.
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