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methyl β-lilacinobioside | 130855-19-5

中文名称
——
中文别名
——
英文名称
methyl β-lilacinobioside
英文别名
Qui3Me(b1-4)b-Dig1Me3Me;(2S,3R,4S,5R,6R)-2-[(2R,3R,4S,6R)-4,6-dimethoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxane-3,5-diol
methyl β-lilacinobioside化学式
CAS
130855-19-5
化学式
C15H28O8
mdl
——
分子量
336.383
InChiKey
SXIOJEVKCQPWHX-QXWQYTELSA-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

物化性质

  • 沸点:
    467.3±45.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.6
  • 重原子数:
    23
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    95.8
  • 氢给体数:
    2
  • 氢受体数:
    8

SDS

SDS:d06c345aa4c9672ac77dc32b25322d28
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反应信息

  • 作为产物:
    描述:
    methyl 4-O-(2,4-di-O-benzoyl-D-thevetopyranosyl)-D-cymaropyranoside 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 生成 methyl β-lilacinobioside
    参考文献:
    名称:
    Expeditious synthesis of saponin P57, an appetite suppressant from Hoodia plants
    摘要:
    孕烷糖苷P57,一种来自Hoodia的食欲抑制成分,被迅速合成,其特点是从地高辛制备了苷元Hoodigogenin A,并通过糖基O-炔基苯甲酸酯作为供体来组装脱氧三糖。
    DOI:
    10.1039/c2cc34404a
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文献信息

  • An appetite suppressant from Hoodia species
    作者:Fanie R. van Heerden、R. Marthinus Horak、Vinesh J. Maharaj、Robert Vleggaar、Jeremiah V. Senabe、Philip J. Gunning
    DOI:10.1016/j.phytochem.2007.05.022
    日期:2007.10
    Studies conducted at the Council for Scientific and Industrial Research (CSIR, South Africa) identified extracts from Hoodia species, in particular Hoodia pilifera and Hoodia gordonii, as possessing appetite suppressing properties. Two pregnane glycosides were isolated by fractionation of the dried stems of H. gordonii. Their structures were determined as 3 beta-[beta-D-thevetopyranosyl-(1 -> 4)-beta-D-cymaropyranosyl- (1 -> 4)-beta-D-cymaropyranosyloxy]-12 beta-tigloyloxy-14 beta-hydroxypregn-5-en-20-one (1) and 3 beta-[beta-D-cymaropyranosyl-(1 -> 4)-beta-D-6-thevetopyranosyl- (1 -> 4)-beta-D-cymaropyranosyl-(1 -> 4)-beta-D-cymaropyranosyloxy]-12 beta-tigloyloxy-14 beta-hydroxypregn-5-en-20-one (2) on the basis of spectroscopic studies and conversion to known compounds. Compounds 1 and 2 were also isolated from H. pilifera. Compound 1 was tested for its appetite suppressant properties in rats by oral gavage at 6.25-50 mg/kg and the results showed that all doses resulted in a decrease of food consumption over an eight day period and a body mass decrease when compared to the control sample receiving only the vehicle. In a comparative study against a fenfluramine control sample, compound 1 resulted in a reduction in food intake over the study period, with a concomitant overall decrease in body weight while fenfluramine resulted in a small decrease in food intake, but an increase in body weight (though less than control group) over the same period of time. (C) 2007 Elsevier Ltd. All rights reserved.
  • Expeditious synthesis of saponin P57, an appetite suppressant from Hoodia plants
    作者:Jian Zhang、Hefang Shi、Yuyong Ma、Biao Yu
    DOI:10.1039/c2cc34404a
    日期:——
    Pregnane glycoside P57, the appetite suppressant component from Hoodia, was synthesized expeditiously, featuring preparation of the aglycone Hoodigogenin A from digoxin and assembly of the deoxytrisaccharide with glycosyl o-alkynylbenzoates as donors.
    孕烷糖苷P57,一种来自Hoodia的食欲抑制成分,被迅速合成,其特点是从地高辛制备了苷元Hoodigogenin A,并通过糖基O-炔基苯甲酸酯作为供体来组装脱氧三糖。
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