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4-ethyl-N-(3,4,5-trimethoxybenzylidene)aniline | 151221-91-9

中文名称
——
中文别名
——
英文名称
4-ethyl-N-(3,4,5-trimethoxybenzylidene)aniline
英文别名
——
4-ethyl-N-(3,4,5-trimethoxybenzylidene)aniline化学式
CAS
151221-91-9
化学式
C18H21NO3
mdl
——
分子量
299.37
InChiKey
LIQFNGGAKXIUPT-XDHOZWIPSA-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:
    436.5±45.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.03
  • 重原子数:
    22.0
  • 可旋转键数:
    6.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    40.05
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

SDS

SDS:250a3f0f654cef8f62171ae048cf8dbe
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-ethyl-N-(3,4,5-trimethoxybenzylidene)aniline 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以76.6%的产率得到4-ethyl-N-(3,4,5-trimethoxybenzyl)aniline
    参考文献:
    名称:
    Synthesis and evaluation of a series of benzylaniline hydrochlorides as potential cytotoxic and antimitotic agents acting by inhibition of tubulin polymerization
    摘要:
    Although certain substituted cis-stilbenes have displayed potent tubulin polymerization inhibitory activity and significant cytotoxicities in cancer cell cultures, these compounds have limited aqueous solubility and are therefore difficult to formulate for in vivo evaluation. A series of water-soluble N-(3,4,5-trimethoxybenzyl)aniline salts has therefore been synthesized in which the olefinic bridge of the stilbenes is replaced by an aminomethylene hydrochloride moiety. A relationship was found between the size of the substituent in the 4-position of the aniline ring and both antitubulin activity and cytotoxicity, such that the smaller the substituent, the greater the potency. The most promising of the newly synthesized compounds was 4-methyl-N-(3,4,5-trimethoxybenzyl)aniline hydrochloride, with an IC50 value of 3.5 muM for inhibition of tubulin polymerization and cytotoxicity for a wide variety of cancer cell lines. The cytotoxicities of the benzylaniline hydrochlorides correlated remarkably well with their antitubulin activities.
    DOI:
    10.1021/jm00071a012
  • 作为产物:
    描述:
    3,4,5-三甲氧基苯甲醛4-乙基苯胺乙醇 为溶剂, 反应 3.0h, 以90.3%的产率得到4-ethyl-N-(3,4,5-trimethoxybenzylidene)aniline
    参考文献:
    名称:
    Synthesis and evaluation of a series of benzylaniline hydrochlorides as potential cytotoxic and antimitotic agents acting by inhibition of tubulin polymerization
    摘要:
    Although certain substituted cis-stilbenes have displayed potent tubulin polymerization inhibitory activity and significant cytotoxicities in cancer cell cultures, these compounds have limited aqueous solubility and are therefore difficult to formulate for in vivo evaluation. A series of water-soluble N-(3,4,5-trimethoxybenzyl)aniline salts has therefore been synthesized in which the olefinic bridge of the stilbenes is replaced by an aminomethylene hydrochloride moiety. A relationship was found between the size of the substituent in the 4-position of the aniline ring and both antitubulin activity and cytotoxicity, such that the smaller the substituent, the greater the potency. The most promising of the newly synthesized compounds was 4-methyl-N-(3,4,5-trimethoxybenzyl)aniline hydrochloride, with an IC50 value of 3.5 muM for inhibition of tubulin polymerization and cytotoxicity for a wide variety of cancer cell lines. The cytotoxicities of the benzylaniline hydrochlorides correlated remarkably well with their antitubulin activities.
    DOI:
    10.1021/jm00071a012
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文献信息

  • Stilbene derivatives as anticancer agents
    申请人:Research Corporation Technologies, Inc.
    公开号:US05430062A1
    公开(公告)日:1995-07-04
    The present invention relates to stilbene derivatives which possess utility as anti-cancer agents. The compounds can be used to treat cancers which are susceptible to treatment therewith, and can be utilized in a method of treating such cancers. Pharmaceutical compositions containing the compounds are disclosed. Three preferred compounds among those disclosed are (Z)-1-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethene, (Z)-1-(4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)ethene, and 4-methyl-3',4',5'-trimethoxybenzylaniline hydrochloride.
    本发明涉及一种具有抗癌作用的苯乙烯生物。这些化合物可用于治疗易于通过其治疗的癌症,并可用于治疗这些癌症的方法中。本文还披露了含有这些化合物的制药组合物。在披露的化合物中,有三种优选的化合物,分别为(Z)-1-(4-甲氧基苯基)-2-(3,4,5-三甲氧基苯基)乙烯,(Z)-1-(4-甲基苯基)-2-(3,4,5-三甲氧基苯基)乙烯和4-甲基-3',4',5'-三甲氧基苯乙胺盐酸盐
  • STILBENE DERIVATIVES AS ANTICANCER AGENTS
    申请人:Research Corporation Technologies, Inc.
    公开号:EP0641301A1
    公开(公告)日:1995-03-08
  • US5430062A
    申请人:——
    公开号:US5430062A
    公开(公告)日:1995-07-04
  • [EN] STILBENE DERIVATIVES AS ANTICANCER AGENTS<br/>[FR] DERIVES DE STILBENE UTILISES COMME AGENTS ANTICANCEREUX
    申请人:——
    公开号:WO1993023357A1
    公开(公告)日:1993-11-25
    [EN] The present invention relates to stilbene derivatives which possess utility as anti-cancer agents. The compounds can be used to treat cancers which are susceptible to treatment therewith, and can be utilized in a method of treating such cancers. Pharmaceutical compositions containing the compounds are disclosed. Three preferred compounds amont those disclosed are (Z)-1-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethene, (Z)-1-(4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)ethene, and 4-methyl-3',4',5'-trimethoxybenzylaniline hydrochloride.
    [FR] Dérivés de stilbène présentant une utilité comme agents anticancéreux. On peut utiliser lesdits composés afin de traiter des cancers susceptibles d'être traités avec ceux-ci, et dans un procédé de traitement desdits cancers. L'invention concerne également des compositions pharmaceutiques contenant lesdits composés. Les composés préférés parmi ceux décrits dans l'invention sont (Z)-1-(4-méthoxyphényl)-2-(3,4,5-triméthoxyphényl)éthène, (Z)-1-(4-méthylphényl)-2-(3,4,5-triméthoxyphényl)éthène, et l'hydrochlorate de 4-méthyl-3',4',5'-triméthoxybenzylaniline.
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