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sesuvioside C | 1312097-82-7

中文名称
——
中文别名
——
英文名称
sesuvioside C
英文别名
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
sesuvioside C化学式
CAS
1312097-82-7
化学式
C29H34O17
mdl
——
分子量
654.579
InChiKey
USZQOCYTRJLIOF-JRHXFWIGSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    -1
  • 重原子数:
    46
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    264
  • 氢给体数:
    9
  • 氢受体数:
    17

上下游信息

  • 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:
    sesuvioside C盐酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 4.0h, 生成 3,5,3’,4’-四羟基-6,7-二甲氧基黄酮L-鼠李糖口服葡萄糖
    参考文献:
    名称:
    Flavonol 3-O-robinobiosides and 3-O-(2″-O-α-rhamnopyranosyl)-robinobiosides from Sesuvium portulacastrum
    摘要:
    Six new flavonol 3-O-robinobiosides and 3-O-(2 ''-O-alpha-L-rhamnopyranosyl)-robinobiosides, sesuviosides A F, were isolated from the aerial portion of Sesuvium portulacastrum together with ecdysterone, adenosine, 2'-O-methyladenosine, and L-tryptophan. The structure elucidations were based on analyses of chemical and spectroscopic data including 1D and 2D-NMR. Sesuviosides A-F and their aglycones exhibited radical scavenging activity using DPPH and ORAC assays. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.04.041
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文献信息

  • Flavonol 3-O-robinobiosides and 3-O-(2″-O-α-rhamnopyranosyl)-robinobiosides from Sesuvium portulacastrum
    作者:Wannaporn Disadee、Chulabhorn Mahidol、Poolsak Sahakitpichan、Somkit Sitthimonchai、Somsak Ruchirawat、Tripetch Kanchanapoom
    DOI:10.1016/j.tet.2011.04.041
    日期:2011.6
    Six new flavonol 3-O-robinobiosides and 3-O-(2 ''-O-alpha-L-rhamnopyranosyl)-robinobiosides, sesuviosides A F, were isolated from the aerial portion of Sesuvium portulacastrum together with ecdysterone, adenosine, 2'-O-methyladenosine, and L-tryptophan. The structure elucidations were based on analyses of chemical and spectroscopic data including 1D and 2D-NMR. Sesuviosides A-F and their aglycones exhibited radical scavenging activity using DPPH and ORAC assays. (C) 2011 Elsevier Ltd. All rights reserved.
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