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(E)-3-(3-methoxyphenyl)-N-phenylacrylamide

中文名称
——
中文别名
——
英文名称
(E)-3-(3-methoxyphenyl)-N-phenylacrylamide
英文别名
3-methoxy-trans-cinnamic acid anilide;3-Methoxy-trans-zimtsaeure-anilid;3-Methoxy-zimtsaeure-anilid;(E)-3-(3-methoxyphenyl)-N-phenylprop-2-enamide
(E)-3-(3-methoxyphenyl)-N-phenylacrylamide化学式
CAS
——
化学式
C16H15NO2
mdl
——
分子量
253.301
InChiKey
LCJBQOLZYUCKLP-ZHACJKMWSA-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):
    3.6
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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

点击查看最新优质反应信息

文献信息

  • Phenylcinnamides as Novel Antimitotic Agents
    作者:Benjamin J. Leslie、Clinton R. Holaday、Tran Nguyen、Paul J. Hergenrother
    DOI:10.1021/jm901805m
    日期:2010.5.27
    Compound 8H is a phenylcinnamide that induces G2/M-phase cell cycle arrest and cell death in cancer cell lines. Here we show that 811 exerts its cytotoxic activity through disruption of microtubule dynamics in vitro and in cell culture. A series of cinnamide derivatives were synthesized and evaluated, and several new compounds were identified that improve on the activity of the parent compound, with IC(50) values for induction of cell death ranging from 1 to 10 mu M. Notably, these compounds retain potency in the HL-60/VCR leukemia cell line, which is resistant to antimitotic cancer drugs vincrisitine and paclitaxel through up-regulation of P-glycoprotein drug efflux pumps. As P-glycoprotein expression is often responsible for drug resistance in cancer and the exclusion of compounds from the central nervous system, 8H and its derivatives merit further examination as potential antimitotic therapeutics, specifically for brain cancers and cancers that are resistant to standard antimitotic agents.
  • Ittyerah; Pandya, Proceedings - Indian Academy of Sciences, Section A, 1941, vol. 13, p. 461,462
    作者:Ittyerah、Pandya
    DOI:——
    日期:——
  • Design, synthesis, antiviral evaluation, and In silico studies of acrylamides targeting nsP2 from Chikungunya virus
    作者:Beatriz Gois de Souza、Shweta Choudhary、Gabriel Gomes Vilela、Gabriel Felipe Silva Passos、Clara Andrezza Crisóstomo Bezerra Costa、Johnnatan Duarte de Freitas、Grazielle Lobo Coelho、Júlia de Andrade Brandão、Leticia Anderson、Ênio José Bassi、João Xavier de Araújo-Júnior、Shailly Tomar、Edeildo Ferreira da Silva-Júnior
    DOI:10.1016/j.ejmech.2023.115572
    日期:2023.10
  • v. Auwers; Brink, Justus Liebigs Annalen der Chemie, 1932, vol. 493, p. 218,231
    作者:v. Auwers、Brink
    DOI:——
    日期:——
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