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ethyl 3-(1-oxidopyridin-4-yl)-1H-pyrazole-5-carboxylate | 723339-27-3

中文名称
——
中文别名
——
英文名称
ethyl 3-(1-oxidopyridin-4-yl)-1H-pyrazole-5-carboxylate
英文别名
——
ethyl 3-(1-oxidopyridin-4-yl)-1H-pyrazole-5-carboxylate化学式
CAS
723339-27-3
化学式
C11H11N3O3
mdl
——
分子量
233.227
InChiKey
PZNKOVOGQWZFBL-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):
    0.89
  • 重原子数:
    17.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    81.92
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

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
  • 下游产品
    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

  • Acyclic pyrazole compounds for the inhibition of mitogen activated protein kinase-activated protein kinase-2
    申请人:Pharmacia Corporation
    公开号:US20040152739A1
    公开(公告)日:2004-08-05
    Compounds are described which inhibit mitogen activated protein kinase-activated protein kinase-2 (MK-2). Methods of making such compounds are described, as well as a method of using them for the inhibition of MK-2, and for the prevention or treatment of a disease or disorder that is mediated by TNF&agr;, where the method involves administering to the subject an MK-2 inhibiting compound of the present invention. Pharmaceutical compositions and kits which contain the present MK-2 inhibiting compounds are also described.
    本文描述了一些抑制有丝分裂原活化蛋白激酶激活蛋白激酶-2(MK-2)的化合物。文中还描述了制备这些化合物的方法,以及使用它们抑制MK-2,预防或治疗由TNFα介导的疾病或障碍的方法,其中该方法涉及向受试者注射本发明的MK-2抑制化合物。文中还描述了包含本MK-2抑制化合物的制药组合物和试剂盒。
  • PYRAZOLE COMPOUNDS AS PROTEIN KINASE INHIBITORS
    申请人:Hanau E. Cathleen
    公开号:US20080113971A1
    公开(公告)日:2008-05-15
    Compounds are described which inhibit mitogen activated protein kinase-activated protein kinase-2 (MK-2). Methods of making such compounds are described, as well as a method of using them for the inhibition of MK-2, and for the prevention or treatment of a disease or disorder that is mediated by TNFα, where the method involves administering to the subject an MK-2 inhibiting compound of the present invention. Pharmaceutical compositions and kits which contain the present MK-2 inhibiting compounds are also described.
    本发明描述了一种抑制有丝分裂原活化蛋白激酶激活蛋白激酶-2(MK-2)的化合物。本发明还描述了制备这种化合物的方法,以及一种使用它们来抑制MK-2并预防或治疗由TNFα介导的疾病或障碍的方法,其中该方法涉及向受试者注射本发明的MK-2抑制化合物。本发明还描述了含有本MK-2抑制化合物的药物组合物和试剂盒。
  • EP1572682A4
    申请人:——
    公开号:EP1572682A4
    公开(公告)日:2008-01-23
  • ACYCLIC PYRAZOLE COMPOUNDS FOR THE INHIBITION OF MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2
    申请人:Pharmacia Corporation
    公开号:EP1572682A2
    公开(公告)日:2005-09-14
  • [EN] ACYCLIC PYRAZOLE COMPOUNDS FOR THE INHIBITION OF MITOGEN ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2<br/>[FR] COMPOSES DE PYRAZOLE ACYCLIQUE POUR L'INHIBITION D'UNE PROTEINE KINASE ACTIVEE PAR MITOGENE / D'UNE PROTEINE KINASE 2 ACTIVEE
    申请人:PHARMACIA CORP
    公开号:WO2004058176A2
    公开(公告)日:2004-07-15
    Compounds are described which inhibit mitogen activated protein kinase-activated protein kinase-2 (MK-2). Methods of making such compounds are described, as well as a method of using them for the inhibition of MK-2, and for the prevention or treatment of a disease or disorder that is mediated by TNFα, where the method involves administering to the subject an MK-2 inhibiting compound of the present invention. Pharmaceutical compositions and kits which contain the present MK-2 inhibiting compounds are also described.
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