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undecyl β-D-galactopyranoside

中文名称
——
中文别名
——
英文名称
undecyl β-D-galactopyranoside
英文别名
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-undecoxyoxane-3,4,5-triol
undecyl β-D-galactopyranoside化学式
CAS
——
化学式
C17H34O6
mdl
——
分子量
334.453
InChiKey
ULDAPNVYSDTSFM-DRRXZNNHSA-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):
    3
  • 重原子数:
    23
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    99.4
  • 氢给体数:
    4
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    十一烷醇ammonium hydroxide三氟化硼乙醚 作用下, 以 甲醇乙腈 为溶剂, 反应 3.2h, 生成 undecyl β-D-galactopyranoside
    参考文献:
    名称:
    The anomeric mixture of some O-galactolipid derivatives is more toxic against cancer cells than either anomer alone
    摘要:
    The anomeric mixture of a series of O-galactolipid derivatives is revealed to be more toxic against several cancer cell lines than their either single component with the pure alpha- or beta-configuration. This interesting phenomenon has been confirmed on pairs of synthesized O-galactosyl anomers bearing length-varied alkyl chains at the lipid end. Furthermore, the most potent mixture was determined inoffensive to a normal cell line tested. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.01.069
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文献信息

  • Konstantinović; Dimitrijević; Radulović, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2002, vol. 41, # 3, p. 598 - 603
    作者:Konstantinović、Dimitrijević、Radulović
    DOI:——
    日期:——
  • Synthesis and properties of new bolaform and macrocyclic galactose-based surfactants obtained by olefin metathesis
    作者:Céline Satgé、Robert Granet、Bernard Verneuil、Yves Champavier、Pierre Krausz
    DOI:10.1016/j.carres.2004.03.003
    日期:2004.5
    A series of galactose-based surfactants with various structures likely to display new interesting properties were synthesized. Four monocatenary surfactants were elaborated by microwave-assisted galactosylation of undecanol or 10-undecenol. These compounds were slightly soluble in water. Their tensioactive properties were determined at 45 degreesC. Olefin metathesis was used to synthesize the two single-chain bolaforms from undec-10-enyl galactopyranosides; two pseudomacrocyclic bolaforms were prepared by grafting two carbamates at O-4 and O-4' sugar positions of the single-chain bolaforms. These four surfactants are insoluble in water and undergo monolayer compression. Cyclization of these bolaforms by olefin metathesis led to macrocyclic surfactant analogues of archaeobacterial membrane components. (C) 2004 Published by Elsevier Ltd.
  • The anomeric mixture of some O-galactolipid derivatives is more toxic against cancer cells than either anomer alone
    作者:Shao-Xing Song、Ming-Li Wu、Xiao-Peng He、Yu-Bo Zhou、Li Sheng、Jia Li、Guo-Rong Chen
    DOI:10.1016/j.bmcl.2012.01.069
    日期:2012.3
    The anomeric mixture of a series of O-galactolipid derivatives is revealed to be more toxic against several cancer cell lines than their either single component with the pure alpha- or beta-configuration. This interesting phenomenon has been confirmed on pairs of synthesized O-galactosyl anomers bearing length-varied alkyl chains at the lipid end. Furthermore, the most potent mixture was determined inoffensive to a normal cell line tested. (C) 2012 Elsevier Ltd. All rights reserved.
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