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2-methylphenyl O-β-D-xylopyranosyl-(1→6)-O-β-D-glucopyranoside

中文名称
——
中文别名
——
英文名称
2-methylphenyl O-β-D-xylopyranosyl-(1→6)-O-β-D-glucopyranoside
英文别名
——
2-methylphenyl O-β-D-xylopyranosyl-(1→6)-O-β-D-glucopyranoside化学式
CAS
——
化学式
C18H26O10
mdl
——
分子量
402.398
InChiKey
YWBIJVWRUHBVAG-ZCLRWAROSA-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):
    -2.36
  • 重原子数:
    28.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    158.3
  • 氢给体数:
    6.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Chemical constituents from the roots of Ampelopsis delavayana and their antibacterial activities
    摘要:
    Two new aromatic glycosides, 2-methylphenyl O-beta-D-xylopyranosyl-(1 -> 6)-O-beta-D-glucopyranoside (1) and 2-methylphenyl O-alpha-arabinofuranosyl( 1 -> 6)-O-beta-glucopyranoside (2), together with eight known compounds were isolated from the roots of Ampelopsis delavayana. Their structures were elucidated on the basis of extensive spectroscopic analysis. Furthermore, the in vitro antibacterial activities of 1 and 2 were investigated using serial twofold dilution in three bacteria including Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus.[GRAPHICS].
    DOI:
    10.1080/14786419.2016.1224875
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文献信息

  • Chemical constituents from the roots of <i>Ampelopsis delavayana</i> and their antibacterial activities
    作者:Shuang-Xi Mei、Xu-Hong Li、Li-Guo Yang、Xiao-Hui Li、Jia-Ying Xie、Qi Yao、Mei Su、Tao Cui、Jing-Kun Wang、Zhao-Yun Zhu
    DOI:10.1080/14786419.2016.1224875
    日期:2017.1.17
    Two new aromatic glycosides, 2-methylphenyl O-beta-D-xylopyranosyl-(1 -> 6)-O-beta-D-glucopyranoside (1) and 2-methylphenyl O-alpha-arabinofuranosyl( 1 -> 6)-O-beta-glucopyranoside (2), together with eight known compounds were isolated from the roots of Ampelopsis delavayana. Their structures were elucidated on the basis of extensive spectroscopic analysis. Furthermore, the in vitro antibacterial activities of 1 and 2 were investigated using serial twofold dilution in three bacteria including Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus.[GRAPHICS].
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