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-[5-(Dimethylamino)-3-(2-methylsulfonylphenothiazin-10-yl)-5-oxopentyl]piperidine-4-carboxylic acid

中文名称
——
中文别名
——
英文名称
1-[5-(Dimethylamino)-3-(2-methylsulfonylphenothiazin-10-yl)-5-oxopentyl]piperidine-4-carboxylic acid
英文别名
1-[5-(dimethylamino)-3-(2-methylsulfonylphenothiazin-10-yl)-5-oxopentyl]piperidine-4-carboxylic acid
1-[5-(Dimethylamino)-3-(2-methylsulfonylphenothiazin-10-yl)-5-oxopentyl]piperidine-4-carboxylic acid化学式
CAS
——
化学式
C26H33N3O5S2
mdl
——
分子量
531.7
InChiKey
IQBJGZVLMBEGAZ-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):
    0.6
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    132
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • METHODS FOR TREATING GI TRACT DISORDERS
    申请人:Neurogastrx, Inc.
    公开号:EP2934540A1
    公开(公告)日:2015-10-28
  • [EN] METHODS FOR TREATING GI TRACT DISORDERS<br/>[FR] MÉTHODES DE TRAITEMENT D'AFFECTIONS DU TRACTUS DIGESTIF
    申请人:NEUROGASTRX INC
    公开号:WO2014105655A1
    公开(公告)日:2014-07-03
    Provided herein are methods, compositions, and kits for the treatment of an enteric nervous system disorder. Such methods may comprise administering to a subject an effective amount of a phenothiazine compound, a peripherally restricted dopamine decarboxylase inhibitor, and/or a peripherally restricted dopamine D2 receptor antagonist that does not substantially inhibit hERG channels
  • [EN] PRODRUGS OF METOPIMAZINE<br/>[FR] PROMÉDICAMENTS DE MÉTOPIMAZINE
    申请人:NEUROGASTRX INC
    公开号:WO2015200369A1
    公开(公告)日:2015-12-30
    Provided herein are methods, compounds, compositions, and kits for the treatment of an enteric nervous system disorder. Such methods may comprise administering to a subject an effective amount of a phenothiazine compound, a peripherally restricted dopamine decarboxylase inhibitor, and/or a peripherally restricted dopamine D2 receptor antagonist that does not substantially inhibit hERG channels.
查看更多