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(3E)-3-[[2-(4-methylpiperazin-1-yl)phenyl]methylidene]-1H-indol-2-one

中文名称
——
中文别名
——
英文名称
(3E)-3-[[2-(4-methylpiperazin-1-yl)phenyl]methylidene]-1H-indol-2-one
英文别名
——
(3E)-3-[[2-(4-methylpiperazin-1-yl)phenyl]methylidene]-1H-indol-2-one化学式
CAS
——
化学式
C20H21N3O
mdl
——
分子量
319.4
InChiKey
GVZDDZHOCZYDBT-SAPNQHFASA-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):
    2.8
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    35.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • Phenoxypropylamine compounds
    申请人:——
    公开号:US20020111358A1
    公开(公告)日:2002-08-15
    The present invention relates to a phenoxypropylamine compound of the formula (I) 1 wherein each symbol is as defined in the specification, an optically active compound thereof or a pharmaceutically acceptable salt thereof and hydrates thereof, which simultaneously show selective affinity for and antagonistic activity against 5-HT 1A receptor, as well as 5-HT reuptake inhibitory activity, and can be used as antidepressants quick in expressing an anti-depressive effect.
    本发明涉及一种公式(I)中的苯氧丙胺化合物: 1 其中每个符号如说明书中所定义,其光学活性化合物或其药物可接受的盐及合物,同时显示出对5-HT 1A 受体的选择性亲和力和拮抗活性,以及5-HT再摄取抑制活性,并且可以用作快速表达抗抑郁效果的抗抑郁药。
  • Benzyl(idene)-lactam derivatives, their preperation and their use as selective (ant)agonists of 5-HT1A- and/or 5-HT1D receptors
    申请人:Pfizer Inc.
    公开号:US20030027812A1
    公开(公告)日:2003-02-06
    The present invention relates to lactam derivatives of the formula 1 wherein R 1 , R 2 , R 3 , A, X, Z, n and the dashed line are defined herein, and pharmaceutical compositions thereof, to processes and intermediates for their preparation, and to their medicinal use as selective agonists and antagonists of serotonin 1 (5-HT 1 ) receptors, specifically, of one or both of the 5-HT 1A and 5-HT 1D receptors. These compounds are useful in treating or preventing migraine, depression and other disorders for which a 5-HT 1 agonist or antagonist is indicated.
    本发明涉及公式1的内酰胺衍生物,其中R1、R2、R3、A、X、Z、n和虚线在此被定义,以及其药物组成物、制备过程和中间体,以及它们作为选择性5-羟色胺1(5-HT1)受体的激动剂和拮抗剂的药用。具体来说,是对5-HT1A和5-HT1D受体中的一个或两个的选择性拮抗剂和激动剂。这些化合物在治疗或预防偏头痛、抑郁症和其他需要5-HT1激动剂或拮抗剂的疾病中非常有用。
  • PHENOXYPROPYLAMINE COMPOUNDS
    申请人:Mitsubishi Pharma Corporation
    公开号:EP1188747B1
    公开(公告)日:2005-09-07
  • BENZYL(IDENE)-LACTAM DERIVATIVES, THEIR PREPARATION AND THEIR USE AS SELECTIVE (ANT)AGONISTS OF 5-HT1A- AND/OR 5-HT1D RECEPTORS
    申请人:PFIZER INC.
    公开号:EP0894085A1
    公开(公告)日:1999-02-03
  • US6462048B2
    申请人:——
    公开号:US6462048B2
    公开(公告)日:2002-10-08
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