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3,4,5-trimethoxyphenyl 6′-O-(5-O-p-coumaroyl)-β-d-apiofuranosyl-β-d-glucopyranoside

中文名称
——
中文别名
——
英文名称
3,4,5-trimethoxyphenyl 6′-O-(5-O-p-coumaroyl)-β-d-apiofuranosyl-β-d-glucopyranoside
英文别名
hedyotosides C;[(3S,4R,5R)-3,4-dihydroxy-5-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methoxy]oxolan-3-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate
3,4,5-trimethoxyphenyl 6′-O-(5-O-p-coumaroyl)-β-d-apiofuranosyl-β-d-glucopyranoside化学式
CAS
——
化学式
C29H36O15
mdl
——
分子量
624.596
InChiKey
GJEJBLXWDOIAKP-JYHPETRWSA-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):
    -0.3
  • 重原子数:
    44
  • 可旋转键数:
    13
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    212
  • 氢给体数:
    6
  • 氢受体数:
    15

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Five new phenolic glycosides from Hedyotis scandens
    摘要:
    Five new phenolic glycosides, hedyotosides A-E (1-5), including a new cyanogenic glycoside (1), along with 10 known compounds (6-15) were isolated from the whole plants of Hedyotis scandens. The structures of compounds 1-5 were established by extensive spectroscopic analyses and acid hydrolysis. All the isolated compounds were evaluated for their in vitro antiviral activity against respiratory syncytial virus (RSV) with cytopathic effect (CPE) reduction assay. Compounds 6 and 15 showed anti-RSV effects with IC50 values of 20 and 25 mu g/mL, respectively. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.12.077
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文献信息

  • Five new phenolic glycosides from Hedyotis scandens
    作者:Guo-Cai Wang、Tao Li、Fang-Ye Deng、Yao-Lan Li、Wen-Cai Ye
    DOI:10.1016/j.bmcl.2012.12.077
    日期:2013.3
    Five new phenolic glycosides, hedyotosides A-E (1-5), including a new cyanogenic glycoside (1), along with 10 known compounds (6-15) were isolated from the whole plants of Hedyotis scandens. The structures of compounds 1-5 were established by extensive spectroscopic analyses and acid hydrolysis. All the isolated compounds were evaluated for their in vitro antiviral activity against respiratory syncytial virus (RSV) with cytopathic effect (CPE) reduction assay. Compounds 6 and 15 showed anti-RSV effects with IC50 values of 20 and 25 mu g/mL, respectively. (c) 2012 Elsevier Ltd. All rights reserved.
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