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Acetic acid (2S,3R,4S,5R)-4,5,6-trihydroxy-2-methyl-tetrahydro-pyran-3-yl ester | 73983-27-4

中文名称
——
中文别名
——
英文名称
Acetic acid (2S,3R,4S,5R)-4,5,6-trihydroxy-2-methyl-tetrahydro-pyran-3-yl ester
英文别名
[(2S,3R,4S,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl] acetate
Acetic acid (2S,3R,4S,5R)-4,5,6-trihydroxy-2-methyl-tetrahydro-pyran-3-yl ester化学式
CAS
73983-27-4
化学式
C8H14O6
mdl
——
分子量
206.196
InChiKey
MXTSNLGDJVRMEB-VAYLDTTESA-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):
    -1.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    96.2
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

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文献信息

  • Novel Flavonoids from the Leaves of<i>Actinidia valvata</i>Dunn: Structural Elucidation and Antioxidant Activity
    作者:Hai-Liang Xin、Ying-Chun Wu、Yong-Hua Su、Jia-Yu Sheng、Chang-Quan Ling
    DOI:10.1055/s-0030-1250113
    日期:2011.1
    Two novel flavonoids, kaempferol 3-O-α-L-rhamnopyranosyl (1–3) (2,4-di-O-acetyl-α-L-rhamnopyranosyl) (1–6) β-D-galactopyranoside (1) and kaempferol 3-O-α-L-rhamnopyranosyl (1–3) (4-O-acetyl-α-L-rhamnopyranosyl) (1–6) β-D-galactopyranoside (2), along with three known ones, kaempferol-3-O-β-D-galactopyranoside (3), kaempferol (4), and 7-hydroxychromone (5), have been isolated from the leaves of Actinidia valvata Dunn, and their structures were elucidated based on spectroscopic methods. Compounds 1 – 3 exhibited dose-dependent activity in scavenging 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radicals, superoxide anion radicals, and hydroxyl radicals, and inhibited lipid peroxidation of mouse liver homogenate in vitro.
    两种新型黄酮类化合物山奈酚 3-O-α-L-rhamnopyranosyl (1-3) (2,4-di-O-acetyl-α-L-rhamnopyranosyl) (1-6) δ²-D-galactopyranoside (1) 和山奈酚 3-O-α-L-rhamnopyranosyl (1-3) (4-O-acetyl-α-L-rhamnopyranosyl) (1-6) δ²-D-galactopyranoside (2)、以及山奈酚-3-O-δ-D-喃半乳糖苷(3)、山奈酚(4)和 7-羟基色酮(5)这三种已知的山奈酚-3-O-δ-D-喃半乳糖苷,并根据光谱方法阐明了它们的结构。化合物 1â-â3 在体外清除 1,1-二苯基-2-苦基DPPH)自由基、超氧阴离子自由基和羟自由基方面表现出剂量依赖性活性,并能抑制小鼠肝匀浆的脂质过氧化反应。
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