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(S)-1-(2-(((S)-2-hydroxydodecyl)oxy)ethoxy)hexadecan-2-ol | 1616683-31-8

中文名称
——
中文别名
——
英文名称
(S)-1-(2-(((S)-2-hydroxydodecyl)oxy)ethoxy)hexadecan-2-ol
英文别名
——
(S)-1-(2-(((S)-2-hydroxydodecyl)oxy)ethoxy)hexadecan-2-ol化学式
CAS
1616683-31-8
化学式
C30H62O4
mdl
——
分子量
486.82
InChiKey
WZTCJOGLONQNPC-KYJUHHDHSA-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):
    8.36
  • 重原子数:
    34.0
  • 可旋转键数:
    29.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    58.92
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

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:
    4-二甲氨基吡啶 、 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 正丁基锂p-toluenesulfonylhydrazidesodium acetate甲基磺酰氯三乙胺 作用下, 以 四氢呋喃乙二醇二甲醚正己烷二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 21.83h, 生成 (S)-1-(2-(((S)-2-hydroxydodecyl)oxy)ethoxy)hexadecan-2-ol
    参考文献:
    名称:
    New cytotoxic annonaceous acetogenin mimetics having a nitrogen-heterocyclic terminal and their application to cell imaging
    摘要:
    A terminal unsaturated lactone or its equivalent is commonly believed to be essential for the cytotoxicity of natural annonaceous acetogenins and their artificial mimetics. In this work, we discovered a series of new cytotoxic ethylene glycol ether-containing mimetics, in which a variety of simple aliphatic nitrogen-heterocycles were introduced to replace the lactone terminal of AA005 (1), a representative bioactive polyether mimic identified from our previous research, for the first time. Among these, mimic 4 bearing a terminal piperazine was found to be the most potent compound against the proliferation of three cancer cells. Based on our new findings, a fluorescent probe 7 was also developed and successfully applied to the imaging of cancer cells. This work provides a new strategy for developing simpler cytotoxic mimetics of natural annonaceous acetogenins and molecular tools for biological imaging. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2014.05.047
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