摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-Chloro-6-(trifluoromethyl)isoquinoline | 1196152-92-7

中文名称
——
中文别名
——
英文名称
1-Chloro-6-(trifluoromethyl)isoquinoline
英文别名
——
1-Chloro-6-(trifluoromethyl)isoquinoline化学式
CAS
1196152-92-7
化学式
C10H5ClF3N
mdl
——
分子量
231.6
InChiKey
UPVQNMWLCOMNPH-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

物化性质

  • 沸点:
    296.3±35.0 °C(Predicted)
  • 密度:
    1.427±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • [EN] AMIDE DERIVATIVES AS Nav1.7 and Nav1.8 BLOCKERS<br/>[FR] DÉRIVÉS D'AMIDE UTILISÉS EN TANT QUE BLOQUEURS DE NAV1,7 ET DE NAV1,8
    申请人:RAQUALIA PHARMA INC
    公开号:WO2018235851A1
    公开(公告)日:2018-12-27
    The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the Nav1.7 and Nav1.8 channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及酰胺衍生物,具有对Nav1.7和Nav1.8通道的阻塞活性,并且在涉及电压门控通道的疾病和疾病的治疗或预防中有用。该发明还涉及包含这些化合物的药物组合物,以及在涉及电压门控通道的疾病的预防或治疗中使用这些化合物和组合物。
  • Amide derivatives as Nav1.7 and Nav1.8 blockers
    申请人:RaQualia Pharma Inc.
    公开号:US11154544B2
    公开(公告)日:2021-10-26
    The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the Nav1.7 and Nav1.8 channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved.
    本发明涉及对电压门控通道(如 Nav1.7 和 Nav1.8 通道)具有阻断活性的酰胺衍生物,它们可用于治疗或预防涉及电压门控通道的紊乱和疾病。本发明还涉及包含这些化合物的药物组合物,以及这些化合物和组合物在预防或治疗涉及电压门控通道的此类疾病中的用途。
  • EP3487839B1
    申请人:——
    公开号:EP3487839B1
    公开(公告)日:2020-12-23
  • AMIDE DERIVATIVES AS NAV1.7 AND NAV1.8 BLOCKERS
    申请人:RaQualia Pharma Inc.
    公开号:EP3487839A1
    公开(公告)日:2019-05-29
查看更多