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quercetin 3-O-((β-D-glucopyranosyl-(1->3)-(4-O-(E-p-coumaroyl))-α-L-rhamnopyranosyl-(1->6)-β-D-galactopyranoside))-7-O-α-L-rhamnopyranoside | 1011263-46-9

中文名称
——
中文别名
——
英文名称
quercetin 3-O-((β-D-glucopyranosyl-(1->3)-(4-O-(E-p-coumaroyl))-α-L-rhamnopyranosyl-(1->6)-β-D-galactopyranoside))-7-O-α-L-rhamnopyranoside
英文别名
[(2S,3S,4S,5R,6R)-6-[[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate
quercetin 3-O-((β-D-glucopyranosyl-(1->3)-(4-O-(E-p-coumaroyl))-α-L-rhamnopyranosyl-(1->6)-β-D-galactopyranoside))-7-O-α-L-rhamnopyranoside化学式
CAS
1011263-46-9
化学式
C48H56O27
mdl
——
分子量
1064.96
InChiKey
YMZBVMSUANSVLO-MMGDPGAJSA-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):
    -1.9
  • 重原子数:
    75
  • 可旋转键数:
    15
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    430
  • 氢给体数:
    15
  • 氢受体数:
    27

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Flavonoid characterization and in vitro antioxidant activity of Aconitum anthora L. (Ranunculaceae)
    摘要:
    In this paper, we report studies on morphological, phytochemical, and biological aspects of a population belonging to Aconitum anthora L. Two compounds, quercetin 3-O-((beta-D-glucopyranosyl-(1 -> 3)-(4-O-(E-p-coumaroyl))-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-galactopyranoside))-7-O-CX-L-rhamnopyranoside (1) and kaempferol 3-O-((beta-D-glucopyranosyl-(1 -> 3)-(4-O-(E-p-coumaroyl))-alpha-L-rhamnopyranosyl-(1 -> 6) -+6)-beta-D-galactopyranoside))-7-O-alpha-C-L-rhamnopyranoside (2), together with two known flavonol glycosides (3-4) were isolated and identified from A. anthora. The antioxidant activity of the four identified flavonoids was screened by three in vitro tests. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2007.12.009
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