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1-(4-Hydroxy-5-nitro-biphenyl-3-yl)-ethanone | 84942-37-0

中文名称
——
中文别名
——
英文名称
1-(4-Hydroxy-5-nitro-biphenyl-3-yl)-ethanone
英文别名
1-(2-Hydroxy-3-nitro-5-phenylphenyl)ethanone
1-(4-Hydroxy-5-nitro-biphenyl-3-yl)-ethanone化学式
CAS
84942-37-0
化学式
C14H11NO4
mdl
——
分子量
257.246
InChiKey
LUDUGHXKAXSMGX-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):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    83.1
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • RXR modulators with improved pharmacologic profile
    申请人:——
    公开号:US20040049072A1
    公开(公告)日:2004-03-11
    The present invention provides a novel class of RXR modulator compounds that exhibit an improved pharmacologic profile relative to the profile of previously studied RXR modulators, including those that share common structural features with the presently claimed modulators. The present invention also provides synthetic methods for preparing these compounds as well as pharmaceutical compositions incorporating these novel compounds and methods for the therapeutic use of such compounds and pharmaceutical compositions.
    本发明提供了一种新型的RXR调节剂化合物,相对于先前研究过的RXR调节剂,包括那些与目前所声称的调节剂具有共同结构特征的化合物,表现出改进的药理学特性。本发明还提供了合成这些化合物的方法,以及包含这些新型化合物的药物组合物和这些化合物和药物组合物的治疗用途的方法。
  • BURDESKA, K., SYNTHESIS, BRD, 1982, N 11, 940-942
    作者:BURDESKA, K.
    DOI:——
    日期:——
  • RXR MODULATORS WITH IMPROVED PHARMACOLOGIC PROFILE
    申请人:LIGAND PHARMACEUTICALS INCORPORATED
    公开号:EP1216221A2
    公开(公告)日:2002-06-26
  • US6593493B1
    申请人:——
    公开号:US6593493B1
    公开(公告)日:2003-07-15
  • [EN] RXR MODULATORS WITH IMPROVED PHARMACOLOGIC PROFILE<br/>[FR] MODULATEURS RXR A PROFIL PHARMACOLOGIQUE AMELIORE
    申请人:LIGAND PHARM INC
    公开号:WO2001019770A2
    公开(公告)日:2001-03-22
    The present invention provides a novel class of RXR modulator compounds that exhibit an improved pharmacologic profile relative to the profile of previously studied RXR modulators, including those that share common structural features with the presently claimed modulators. The present invention also provides synthetic methods for preparing these compounds as well as pharmaceutical compositions incorporating these novel compounds and methods for the therapeutic use of such compounds and pharmaceutical compositions.
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