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(9Z,9a(2)Z)-N,Na(2)-1,3-Propanediylbis[9-octadecenamide] | 5518-21-8

中文名称
——
中文别名
——
英文名称
(9Z,9a(2)Z)-N,Na(2)-1,3-Propanediylbis[9-octadecenamide]
英文别名
(Z)-N-[3-[[(Z)-octadec-9-enoyl]amino]propyl]octadec-9-enamide
(9Z,9a(2)Z)-N,Na(2)-1,3-Propanediylbis[9-octadecenamide]化学式
CAS
5518-21-8
化学式
C39H74N2O2
mdl
——
分子量
603.0
InChiKey
ZSJXKBFCSWUGLX-CLFAGFIQSA-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):
    14.2
  • 重原子数:
    43
  • 可旋转键数:
    34
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    58.2
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • Multimeric Oleamide Derivative Having Connexin-26 Inhibiting Potency and Use Thereof in Cancer Therapy, etc.
    申请人:Nojima Hiroshi
    公开号:US20080089924A1
    公开(公告)日:2008-04-17
    The present invention relates to multimeric oleamide derivatives having connexin 26 inhibitory activities and embraces the dimer oleamide derivatives represented by the following formula (1) or a pharmacologically acceptable salt thereof: where n denotes an integer of 3, 5, or 8. The novel oleamide derivatives of the present invention can be used not only as research reagents, but also in a wide industrial field because they exhibit useful bioactivities such as cancer metastasis/growth inhibition. Thus they have various applications, such as in medicines, supplements, and functional foods, in addition to cancer-preventive and cancer-therapeutic drugs.
    本发明涉及具有connexin 26抑制活性的多聚性油酰胺衍生物,并包括由以下式(1)表示的二聚体油酰胺衍生物或其药理学可接受的盐:其中n表示3、5或8的整数。本发明的新型油酰胺衍生物不仅可以用作研究试剂,还可以在广泛的工业领域中使用,因为它们表现出有用的生物活性,如癌症转移/生长抑制。因此,它们具有各种应用,如在药物、补充剂和功能性食品中,除了癌症预防和癌症治疗药物。
  • US7846972B2
    申请人:——
    公开号:US7846972B2
    公开(公告)日:2010-12-07
  • [EN] FATTY ACID ANALOGS AND METHODS OF USE THEREOF<br/>[FR] ANALOGUES D'ACIDE GRAS ET LEURS PROCÉDÉS D'UTILISATION
    申请人:UNIV CALIFORNIA
    公开号:WO2016168469A1
    公开(公告)日:2016-10-20
    The present disclosure provides lipidoid compounds, and compositions comprising the lipidoid compounds and a nucleic acid. The present disclosure provides methods of making a subject lipidoid. The present disclosure provides a method of delivering a target nucleic acid to a cell, using a lipidoid composition of the present disclosure. The present disclosure provides a method of delivering a gene product to an individual, using a lipidoid composition of the present disclosure.
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