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squarrosanin C

中文名称
——
中文别名
——
英文名称
squarrosanin C
英文别名
[(10R,11R)-10-[(14R,15S,19S)-19-[(11R,12S)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-12-[(1R,2S,3R)-1,2,3-trihydroxy-3-(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)propyl]-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-6-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate
squarrosanin C化学式
CAS
——
化学式
C82H54O51
mdl
——
分子量
1855.3
InChiKey
WWLCHBQSPPBLEU-FVSDXFKUSA-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):
    2.7
  • 重原子数:
    133
  • 可旋转键数:
    12
  • 环数:
    17.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    890
  • 氢给体数:
    31
  • 氢受体数:
    51

反应信息

  • 作为反应物:
    描述:
    squarrosanin C硫酸 作用下, 反应 8.0h, 生成 没食子酸鞣花酸
    参考文献:
    名称:
    Flavonol glucuronides and C-glucosidic ellagitannins from Melaleuca squarrosa
    摘要:
    Two flavonoids and three ellagitannins, squarrosanins A, B, and C, were isolated from the leaves of Melaleuca squarrosa. The flavonoids were characterized structurally as kaempferol-3-O-(2 ''-O-galloyl)-glucuronide and herbacetin-3-O-glucuronide, while the ellagitannins were characterized as monomeric and dimeric C-glucosidic ellagitannins by application of spectroscopic and chemical methods. The antioxidant effect of the polyphenolic constituents of the M. squarrosa leaves was also examined in vitro, and C-glucosidic tannins including oligomers were shown to be more effective radical scavengers against 1,1diphenyl-2-picrylhydi-azyl (DPPH) than flavonoids and ordinary ellagitannins. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2008.04.004
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文献信息

  • Flavonol glucuronides and C-glucosidic ellagitannins from Melaleuca squarrosa
    作者:Morio Yoshimura、Hideyuki Ito、Kyoko Miyashita、Tsutomu Hatano、Shoko Taniguchi、Yoshiaki Amakura、Takashi Yoshida
    DOI:10.1016/j.phytochem.2008.04.004
    日期:2008.12
    Two flavonoids and three ellagitannins, squarrosanins A, B, and C, were isolated from the leaves of Melaleuca squarrosa. The flavonoids were characterized structurally as kaempferol-3-O-(2 ''-O-galloyl)-glucuronide and herbacetin-3-O-glucuronide, while the ellagitannins were characterized as monomeric and dimeric C-glucosidic ellagitannins by application of spectroscopic and chemical methods. The antioxidant effect of the polyphenolic constituents of the M. squarrosa leaves was also examined in vitro, and C-glucosidic tannins including oligomers were shown to be more effective radical scavengers against 1,1diphenyl-2-picrylhydi-azyl (DPPH) than flavonoids and ordinary ellagitannins. (c) 2008 Elsevier Ltd. All rights reserved.
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