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4-[4-(4-Hydroxyphenyl)-1-phenylpyrrol-3-yl]phenol | 1449242-76-5

中文名称
——
中文别名
——
英文名称
4-[4-(4-Hydroxyphenyl)-1-phenylpyrrol-3-yl]phenol
英文别名
4-[4-(4-hydroxyphenyl)-1-phenylpyrrol-3-yl]phenol
4-[4-(4-Hydroxyphenyl)-1-phenylpyrrol-3-yl]phenol化学式
CAS
1449242-76-5
化学式
C22H17NO2
mdl
——
分子量
327.382
InChiKey
JNDKQYDHQPZBMK-UHFFFAOYSA-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):
    4.9
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    45.4
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    FACILE SYNTHESIS AND ESTROGENIC ACTIVITY OF ARYLPYRROLE-BASED BISPHENOL DERIVATIVES
    摘要:
    Novel estrogen candidates 6a and 6b incorporating arylpyrrole bisphenol structure were synthesized in only three steps from commercially available materials by means of McMurry coupling and an unexpected BBr3-mediated aromatization. These compounds showed ER alpha-binding affinity in competitive binding assay and estrogenic activity in MCF-7 cell proliferation assay.
    DOI:
    10.3987/com-12-s(n)56
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文献信息

  • FACILE SYNTHESIS AND ESTROGENIC ACTIVITY OF ARYLPYRROLE-BASED BISPHENOL DERIVATIVES
    作者:Yasuyuki Endo、Kiminori Ohta、Fumi Taguchi
    DOI:10.3987/com-12-s(n)56
    日期:——
    Novel estrogen candidates 6a and 6b incorporating arylpyrrole bisphenol structure were synthesized in only three steps from commercially available materials by means of McMurry coupling and an unexpected BBr3-mediated aromatization. These compounds showed ER alpha-binding affinity in competitive binding assay and estrogenic activity in MCF-7 cell proliferation assay.
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