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6-(N-2,2,2-trifluoroethyl-N-isobutyl)amino-4-trifluoromethyl-2(1H)-quinolinone | 328948-70-5

中文名称
——
中文别名
——
英文名称
6-(N-2,2,2-trifluoroethyl-N-isobutyl)amino-4-trifluoromethyl-2(1H)-quinolinone
英文别名
6-[2-methylpropyl(2,2,2-trifluoroethyl)amino]-4-(trifluoromethyl)-1H-quinolin-2-one
6-(N-2,2,2-trifluoroethyl-N-isobutyl)amino-4-trifluoromethyl-2(1H)-quinolinone化学式
CAS
328948-70-5
化学式
C16H16F6N2O
mdl
——
分子量
366.306
InChiKey
YUVKNNMYHSJKIV-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):
    4.3
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • [EN] ANTI-CANCER NUCLEAR HORMONE RECEPTOR-TARGETING COMPOUNDS<br/>[FR] COMPOSÉS CIBLANT DES RÉCEPTEURS HORMONAUX NUCLÉAIRES ANTICANCÉREUX
    申请人:NUVATION BIO INC
    公开号:WO2021097046A1
    公开(公告)日:2021-05-20
    The disclosure relates to anti-cancer compounds which are anti-cancer PARP inhibitors of formula Al, A2, A3 or A4 conjugated by a linker to a steroid, whereby the steroid targets the conjugate to the nucleus, as well as to methods for their preparation and use. (I)
    该披露涉及抗癌化合物,这些化合物是公式Al、A2、A3或A4的抗癌PARP抑制剂,通过连接剂与类固醇结合,从而使类固醇将该共轭物靶向到细胞核,以及其制备和使用的方法。
  • Bicyclic androgen and progesterone receptor modulator compounds and methods
    申请人:Zhi Lin
    公开号:US20050288350A1
    公开(公告)日:2005-12-29
    The present invention is directed to compounds, pharmaceutical compositions, and methods for modulating processes mediated by AR and PR. More particularly, the invention relates to nonsteroidal compounds and compositions that are high affinity, high specificity agonists, partial agonists (i.e., partial activators and/or tissue-specific activators) and antagonists for AR and PR. Also provided are methods of making such compounds and pharmaceutical compositions, as well as critical intermediates used in their synthesis.
    本发明涉及化合物、制药组合物和调节由AR和PR介导的过程的方法。更具体地,本发明涉及非甾体化合物和组合物,它们是高亲和力、高特异性的AR和PR激动剂、部分激动剂(即部分激活剂和/或组织特异性激活剂)和拮抗剂。还提供了制备这些化合物和制药组合物的方法,以及在它们的合成中使用的关键中间体。
  • BICYCLIC ANDROGEN AND PROGESTERONE RECEPTOR MODULATOR COMPOUNDS AND METHODS
    申请人:LIGAND PHARMACEUTICALS INCORPORATED
    公开号:EP1212303A2
    公开(公告)日:2002-06-12
  • JP2003508387A
    申请人:——
    公开号:JP2003508387A
    公开(公告)日:2003-03-04
  • ANTI-CANCER NUCLEAR HORMONE RECEPTOR-TARGETING COMPOUNDS
    申请人:Nuvation Bio Inc.
    公开号:US20200360523A1
    公开(公告)日:2020-11-19
    The disclosure relates to anti-cancer compounds derived from nuclear steroid receptor binders, to products containing the same, as well as to methods of their use and preparation.
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