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2-(4,4-difluorocyclohexyl)-2-(2-methylpyrimidin-5-yl)ethanamine | 1598428-63-7

中文名称
——
中文别名
——
英文名称
2-(4,4-difluorocyclohexyl)-2-(2-methylpyrimidin-5-yl)ethanamine
英文别名
2-(4,4-Difluorocyclohexyl)-2-(2-methylpyrimidin-5-yl)ethanamine
2-(4,4-difluorocyclohexyl)-2-(2-methylpyrimidin-5-yl)ethanamine化学式
CAS
1598428-63-7
化学式
C13H19F2N3
mdl
——
分子量
255.311
InChiKey
FEWQGNVIIFBGFC-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):
    1.8
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    51.8
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

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文献信息

  • INDOLE CARBOXAMIDE DERIVATIVES AS P2X7 RECEPTOR ANTAGONIST
    申请人:ACTELION PHARMACEUTICALS LTD
    公开号:US20150322008A1
    公开(公告)日:2015-11-12
    The invention relates to indole carboxamide derivatives of formula (I), wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined in the description, their preparation and their use as pharmaceutically active compounds.
    本发明涉及公式(I)中的吲哚羧酰胺衍生物,其中R1、R2、R3、R4、R5和R6如描述中所定义,其制备和用作药学活性化合物。
  • Benzamides-containing compounds and their use in the treatment of epilepsy
    申请人:MINDIMMUNE THERAPEUTICS, INC.
    公开号:US10238654B2
    公开(公告)日:2019-03-26
    The present invention is directed to benzamide-containing compounds of formula I or pharmaceutically acceptable salts thereof which inhibit the P2X7 receptor, and their use in the treatment of epilepsy.
    本发明涉及式 I 的含苯甲酰胺化合物 或其药学上可接受的盐,它们能抑制 P2X7 受体,并可用于治疗癫痫。
  • BENZAMIDES
    申请人:H. Lundbeck A/S
    公开号:EP2906546A1
    公开(公告)日:2015-08-19
  • INDOLE CARBOXAMIDE DERIVATIVES AS P2X7 RECEPTOR ANTAGONISTS
    申请人:Actelion Pharmaceuticals Ltd.
    公开号:EP2931717B1
    公开(公告)日:2016-12-07
  • Benzamides-Containing Compounds and Their Use in the Treatment of Epilepsy
    申请人:H. Lundbeck A/S
    公开号:US20170202836A1
    公开(公告)日:2017-07-20
    The present invention is directed to benzamide-containing compounds of formula I or pharmaceutically acceptable salts thereof which inhibit the P2X 7 receptor, and their use in the treatment of epilepsy.
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