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6-(4-fluoro-2-methoxyphenyl)-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)pyridazin-3-amine | 1562342-42-0

中文名称
——
中文别名
——
英文名称
6-(4-fluoro-2-methoxyphenyl)-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)pyridazin-3-amine
英文别名
——
6-(4-fluoro-2-methoxyphenyl)-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)pyridazin-3-amine化学式
CAS
1562342-42-0
化学式
C21H29FN4O
mdl
——
分子量
372.486
InChiKey
SYGWNGZPDLGJKH-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):
    3.4
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    50.3
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • 1,4-DISUBSTITUTED PYRIDAZINE ANALOGS THERE OF AND METHODS FOR TREATING SMN-DEFICIENCY-RELATED CONDITIONS
    申请人:NOVARTIS AG
    公开号:US20170290828A1
    公开(公告)日:2017-10-12
    The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof; a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.
    本发明提供了式I的化合物或其药学上可接受的盐;制备本发明化合物的方法以及其治疗用途。本发明还提供了具有药理活性剂的组合物和制药组合物。
  • Urea Derivative
    申请人:Kurata Hitoshi
    公开号:US20070249620A1
    公开(公告)日:2007-10-25
    The present invention relates to a urea derivative or a pharmacologically acceptable salt thereof having an excellent DGAT inhibitory effect. A urea derivative having the formula: [wherein R 1 is a C 6 -C 10 aryl group which may be independently mono- to pentasubstituted by a group selected from Substituent Group a or others; R is a C 6 -C 10 aryl group which may be independently mono- to pentasubstituted by a group selected from Substituent Group a or others; E is a group having the formula (II) or the formula (III) (wherein R 3 is a hydrogen atom or others; R 4 and R 5 , which are the same or different, are a hydrogen atom or others; X and U, which are the same or different, are a group represented by the formula CH or others; m and n, which are the same or different, are I or another number) or others; and A is a group represented by the formula —NH—C(═O)— or others], or a pharmacologically acceptable salt thereof.
    本发明涉及一种具有出色DGAT抑制作用的脲衍生物或其药理学上可接受的盐。其中,该脲衍生物具有以下公式:[式中,R1是C6-C10芳基,可以独立地被来自置换基团a或其他的基团单独到五重取代;R是C6-C10芳基,可以独立地被来自置换基团a或其他的基团单独到五重取代;E是具有公式(II)或公式(III)的基团(其中,R3是氢原子或其他;R4和R5相同或不同,是氢原子或其他;X和U相同或不同,是由公式CH或其他表示的基团;m和n相同或不同,是I或其他数字)或其他;A是由公式—NH—C(═O)—或其他表示的基团],或其药理学上可接受的盐。
  • 1,4-disubstituted pyridazine analogs there of and methods for treating SMN-deficiency-related conditions
    申请人:Cheung Atwood Kim
    公开号:US08729263B2
    公开(公告)日:2014-05-20
    The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof; a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.
    本发明提供了公式I的化合物或其药学上可接受的盐;一种制造该发明化合物的方法以及其治疗用途。本发明还提供了一种药理活性剂的组合和制药组合物。
  • 1,4-disubstituted pyridazine analogs thereof and methods for treating SMN-deficiency-related conditions
    申请人:Novartis AG
    公开号:US11229648B2
    公开(公告)日:2022-01-25
    The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof; a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.
    本发明提供了一种式 I 的化合物或其药学上可接受的盐; 一种制造本发明化合物的方法及其治疗用途。本发明还提供了一种药理活性剂组合和药物组合物。
  • 1,4-DISUBSTITUTED PYRIDAZINE ANALOGS AND METHODS FOR TREATING SMN-DEFICIENCY-RELATED CONDITIONS
    申请人:Novartis AG
    公开号:EP2885288A1
    公开(公告)日:2015-06-24
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