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(24S)-12α,16β,24-trihydroxy-9,19-cyclolanostan-3β-yl β-D-glucopyranoside | 1260512-86-4

中文名称
——
中文别名
——
英文名称
(24S)-12α,16β,24-trihydroxy-9,19-cyclolanostan-3β-yl β-D-glucopyranoside
英文别名
(2R,3R,4S,5S,6R)-2-[[(1R,3R,6S,8R,11S,12S,14S,15R,16R,17S)-14,17-dihydroxy-15-[(2R,5S)-5-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(24S)-12α,16β,24-trihydroxy-9,19-cyclolanostan-3β-yl β-D-glucopyranoside化学式
CAS
1260512-86-4
化学式
C36H62O9
mdl
——
分子量
638.883
InChiKey
FLVNLKYUXMNGEM-UWURSDJTSA-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):
    4.4
  • 重原子数:
    45
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    160
  • 氢给体数:
    7
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    (24S)-12α,16β,24-trihydroxy-9,19-cyclolanostan-3β-yl β-D-glucopyranosidealpha-L-rhamnosidase 作用下, 反应 96.0h, 以6.5 mg的产率得到(24S)-9,19-cyclolanostane-3β,12α,16β,24-tetrol
    参考文献:
    名称:
    Cycloartane glycosides from the rhizomes of Curculigo orchioides
    摘要:
    Cycloartane glycosides (1-9) were Isolated from rhizomes of Curculigo orchioides (Hypoxidaceae) and this structures were determined by spectroscopic analysis and a few chemical transformations Cytotoxic activity of glycosides (1-9) and their common aglycone (1a) against HL-60 human promyelocytic leukemia cells was also examined (C) 2010 Elsevier Ltd All lights reserved
    DOI:
    10.1016/j.phytochem.2010.09.005
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文献信息

  • Cycloartane glycosides from the rhizomes of Curculigo orchioides
    作者:Akihito Yokosuka、Koji Sato、Yoshihiro Mimaki
    DOI:10.1016/j.phytochem.2010.09.005
    日期:2010.12
    Cycloartane glycosides (1-9) were Isolated from rhizomes of Curculigo orchioides (Hypoxidaceae) and this structures were determined by spectroscopic analysis and a few chemical transformations Cytotoxic activity of glycosides (1-9) and their common aglycone (1a) against HL-60 human promyelocytic leukemia cells was also examined (C) 2010 Elsevier Ltd All lights reserved
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