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3-(4-Geranyloxyphenyl)-1-ethanol | 58135-33-4

中文名称
——
中文别名
——
英文名称
3-(4-Geranyloxyphenyl)-1-ethanol
英文别名
2-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenyl]ethanol
3-(4-Geranyloxyphenyl)-1-ethanol化学式
CAS
58135-33-4
化学式
C18H26O2
mdl
——
分子量
274.403
InChiKey
HUEGMMWEUQMMTG-FOWTUZBSSA-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):
    4.8
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    香叶基溴对羟基苯乙醇potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 1.0h, 以85%的产率得到3-(4-Geranyloxyphenyl)-1-ethanol
    参考文献:
    名称:
    Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist
    摘要:
    A series of 29 oxyprenylated and azoprenylated phenylpropanoids were chemically synthesized and tested in transfected cultured HepG2 cells by means of the dual-luciferase assay as farnesoid X receptor (FXR) agonists, using the endogenous ligand chenodeoxycholic acid (CDCA) as reference drug. Among the tested molecules, three compounds, namely auraptene, nelumol A, and nelumal A showed a potency comparable to the endogenous ligand, with the latter natural product having a level of activity slightly superior to CDCA. Nelumal A is thus of interest as a valuable potential novel lead compound in the search for FXR agonists. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.03.057
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文献信息

  • [EN] SKIN PIGMENTATION MODIFIERS TO DARKEN OR LIGHTEN THE SKIN<br/>[FR] AGENTS DE MODIFICATION DE LA PIGMENTATION DE LA PEAU EN VUE DE L'ASSOMBRIR OU DE L'ÉCLAIRCIR
    申请人:AFFICHEM
    公开号:WO2016193220A1
    公开(公告)日:2016-12-08
    The present invention relates to a method for changing the pigmentation of a skin, a mucous membrane or hair with a compound of general formula (I), a cosmetic use of said compound of general formula (I), to cosmetic compositions comprising said compound of general formula (I), and to new depigmenting agents.
    本发明涉及一种改变皮肤、粘膜或头发色素的方法,使用一般式(I)的化合物,以及所述一般式(I)的化合物的化妆用途,包括所述一般式(I)的化合物的化妆组合物,以及新的脱色剂。
  • DEPIGMENTING AGENTS TO LIGHTEN THE SKIN
    申请人:Affichem
    公开号:EP3097904A1
    公开(公告)日:2016-11-30
    The present invention relates to a method for lightening a skin or a mucous membrane with a depigmenting agent, a cosmetic use of said depigmenting agent, to cosmetic compositions comprising said agent, and to new depigmenting agents.
    本发明涉及一种使用脱色剂淡化皮肤或粘膜的方法、所述脱色剂的化妆品用途、包含所述脱色剂的化妆品组合物以及新型脱色剂。
  • Nelumal A, the active principle from Ligularia nelumbifolia, is a novel farnesoid X receptor agonist
    作者:Francesco Epifano、Salvatore Genovese、E. James Squires、Matthew A. Gray
    DOI:10.1016/j.bmcl.2012.03.057
    日期:2012.5
    A series of 29 oxyprenylated and azoprenylated phenylpropanoids were chemically synthesized and tested in transfected cultured HepG2 cells by means of the dual-luciferase assay as farnesoid X receptor (FXR) agonists, using the endogenous ligand chenodeoxycholic acid (CDCA) as reference drug. Among the tested molecules, three compounds, namely auraptene, nelumol A, and nelumal A showed a potency comparable to the endogenous ligand, with the latter natural product having a level of activity slightly superior to CDCA. Nelumal A is thus of interest as a valuable potential novel lead compound in the search for FXR agonists. (C) 2012 Elsevier Ltd. All rights reserved.
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