摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

catechin-(4,8)-malvidin-3-O-glucoside | 725223-71-2

中文名称
——
中文别名
——
英文名称
catechin-(4,8)-malvidin-3-O-glucoside
英文别名
(2R,3S)-4-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-8-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol
catechin-(4,8)-malvidin-3-O-glucoside化学式
CAS
725223-71-2
化学式
C38H37O18
mdl
——
分子量
781.701
InChiKey
UWLZMYNJKDRBLI-IYAFGFBISA-O
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):
    2.14
  • 重原子数:
    56
  • 可旋转键数:
    8
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    290
  • 氢给体数:
    12
  • 氢受体数:
    17

反应信息

  • 作为产物:
    描述:
    锦葵素-3-O-葡萄糖苷原花青素B4甲酸 作用下, 以 乙醚 为溶剂, 反应 3.0h, 生成 catechin-(4,8)-malvidin-3-O-glucoside
    参考文献:
    名称:
    The fate of flavanol–anthocyanin adducts in wines: Study of their putative reaction patterns in the presence of acetaldehyde
    摘要:
    Methylmethine bridged flavanol-anthocyanin dimeric adducts (F-A) were synthesised by hemisynthesis using catechin, acetaldehyde and F-A adducts as precursors in order to simulate putative reactions undergoing in red wine. The products obtained, catechin-methylmethine-catechin-malvidin-3-O-glucose and methylmethine-(catechin-malvidin-3-O-glucose), were analysed by HPLC-ESI-MS. The fragmentation patterns allowed the confirmation of the structures. These compounds were investigated and found in wine samples (2-year-old table wine and 10-year-old Port wine), thus confirming their formation in vino as a result of flavanol-anthocyanin adducts transformations. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.foodchem.2010.01.060
点击查看最新优质反应信息

文献信息

  • The fate of flavanol–anthocyanin adducts in wines: Study of their putative reaction patterns in the presence of acetaldehyde
    作者:Frederico Nave、Natércia Teixeira、Nuno Mateus、Victor de Freitas
    DOI:10.1016/j.foodchem.2010.01.060
    日期:2010.8
    Methylmethine bridged flavanol-anthocyanin dimeric adducts (F-A) were synthesised by hemisynthesis using catechin, acetaldehyde and F-A adducts as precursors in order to simulate putative reactions undergoing in red wine. The products obtained, catechin-methylmethine-catechin-malvidin-3-O-glucose and methylmethine-(catechin-malvidin-3-O-glucose), were analysed by HPLC-ESI-MS. The fragmentation patterns allowed the confirmation of the structures. These compounds were investigated and found in wine samples (2-year-old table wine and 10-year-old Port wine), thus confirming their formation in vino as a result of flavanol-anthocyanin adducts transformations. (C) 2010 Elsevier Ltd. All rights reserved.
查看更多