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1-(4-(dimethylamino)phenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one | 127034-48-4

中文名称
——
中文别名
——
英文名称
1-(4-(dimethylamino)phenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
英文别名
(E)-1-[4-(dimethylamino)phenyl]-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
1-(4-(dimethylamino)phenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one化学式
CAS
127034-48-4
化学式
C20H23NO4
mdl
——
分子量
341.407
InChiKey
VIFRKOWCKUMHOG-IZZDOVSWSA-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):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    48
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Chalcones: a new class of antimitotic agents
    摘要:
    A series of chalcones was evaluated as antimitotic agents. One of these, (E)-1-(2,5-dimethoxyphenyl)-3-[4-(dimethylamino)phenyl]-2-methyl-2-pr open- 1-one) (73), was found to be an effective antimitotic agent at a concentration of 4 nM in an in vitro HeLa cell test system. When evaluated in experimental tumor models in vivo, this compound exhibited antitumor activity against L1210 leukemia and B16 melanoma.
    DOI:
    10.1021/jm00169a021
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文献信息

  • Substituted arylcycloalkanes, compositions containing them and use thereof
    申请人:——
    公开号:US20030149072A1
    公开(公告)日:2003-08-07
    Substituted arylcycloalkanes, compositions containing them and use thereof. The present invention relates especially to substituted arylcycloalkanes with therapeutic activity, which may be used such as in oncology.
    被取代的芳基环烷烃、含有它们的组合物及其使用。本发明特别涉及具有治疗活性的取代芳基环烷烃,可用于肿瘤学等领域。
  • Chalcones: a new class of antimitotic agents
    作者:Michael L. Edwards、David M. Stemerick、Prasad S. Sunkara
    DOI:10.1021/jm00169a021
    日期:1990.7
    A series of chalcones was evaluated as antimitotic agents. One of these, (E)-1-(2,5-dimethoxyphenyl)-3-[4-(dimethylamino)phenyl]-2-methyl-2-pr open- 1-one) (73), was found to be an effective antimitotic agent at a concentration of 4 nM in an in vitro HeLa cell test system. When evaluated in experimental tumor models in vivo, this compound exhibited antitumor activity against L1210 leukemia and B16 melanoma.
  • EDWARDS, MICHAEL L.;STEMERICK, DAVID M.;SUNKARA, PRASAD S., J. MED. CHEM., 33,(1990) N, C. 1948-1954
    作者:EDWARDS, MICHAEL L.、STEMERICK, DAVID M.、SUNKARA, PRASAD S.
    DOI:——
    日期:——
  • ARYL-CYCLOALCANES SUBSTITUES ET LEUR UTILISATION COMME AGENTS ANTICANCEREUX
    申请人:Aventis Pharma S.A.
    公开号:EP1453783A1
    公开(公告)日:2004-09-08
  • US6887904B2
    申请人:——
    公开号:US6887904B2
    公开(公告)日:2005-05-03
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