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2-[6-(4-hydroxy-3,5-dimethyl-phenyl)-3-oxo-2,3-dihydro-pyridazin-4-yl]-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid methyl ester | 870100-06-4

中文名称
——
中文别名
——
英文名称
2-[6-(4-hydroxy-3,5-dimethyl-phenyl)-3-oxo-2,3-dihydro-pyridazin-4-yl]-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid methyl ester
英文别名
methyl 2-[3-(4-hydroxy-3,5-dimethylphenyl)-6-oxo-1H-pyridazin-5-yl]-1H-pyrrolo[2,3-c]pyridine-5-carboxylate
2-[6-(4-hydroxy-3,5-dimethyl-phenyl)-3-oxo-2,3-dihydro-pyridazin-4-yl]-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid methyl ester化学式
CAS
870100-06-4
化学式
C21H18N4O4
mdl
——
分子量
390.398
InChiKey
OAJNKGCBKABRSW-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):
    2.5
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    117
  • 氢给体数:
    3
  • 氢受体数:
    6

文献信息

  • [EN] PYRIDAZINONE DERIVATIVES, METHODS FOR PRODUCING THEM AND THEIR USE AS PHARMACEUTICALS<br/>[FR] DERIVES DE PYRIDAZINONE, PROCEDES DE PRODUCTION DE CES DERIVES ET LEUR UTILISATION COMME PHARMACEUTIQUES
    申请人:AVENTIS PHARMA GMBH
    公开号:WO2005111018A1
    公开(公告)日:2005-11-24
    The present invention relates to compounds according to the general formula (I), with the definitions of the substituents X, R1 and R2 given below in the text, as well as their physiologically acceptable salts, methods for producing these compounds and their use as pharmaceuticals. Formula (I) These compounds are kinase inhibitors, in particular inhibitors of the kinase GSK­15 30 (glycogen synthase kinase-3ß).
    本发明涉及通式(I)所示的化合物,其中下文给出了取代基X、R1和R2的定义,以及它们的生理上可接受的盐,生产这些化合物的方法以及它们作为药物的用途。通式(I)这些化合物是激酶抑制剂,特别是激酶GSK-15 30(糖原合成酶激酶-3ß)的抑制剂
  • PYRIDAZINONE DERIVATIVES, METHODS FOR THEIR PRODUCTION AND THEIR USE AS PHARMACEUTICALS
    申请人:Hoelder Swen
    公开号:US20070088041A1
    公开(公告)日:2007-04-19
    The present invention relates to compounds according to the general formula (I), with the definitions of the substituents X, R 1 and R 2 given below in the text, as well as their physiologically acceptable salts, methods for producing these compounds and their use as pharmaceuticals. These compounds are kinase inhibitors, in particular inhibitors of the kinase GSK-3β(glycogen synthase kinase-3β).
    本发明涉及符合通式(I)的化合物,其中X,R1和R2的定义如下文所述,以及它们的生理学上可接受的盐,制备这些化合物的方法以及它们作为药物的用途。这些化合物是激酶抑制剂,特别是激酶GSK-3β(糖原合成酶激酶-3β)的抑制剂
  • PYRIDAZINONE DERIVATIVES, METHODS FOR PRODUCING THEM AND THEIR USE AS PHARMACEUTICALS
    申请人:Sanofi-Aventis Deutschland GmbH
    公开号:EP1753743A1
    公开(公告)日:2007-02-21
  • US7709466B2
    申请人:——
    公开号:US7709466B2
    公开(公告)日:2010-05-04
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