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2-(1-Methylethyl)-5-nitro-2H-indazole

中文名称
——
中文别名
——
英文名称
2-(1-Methylethyl)-5-nitro-2H-indazole
英文别名
5-nitro-2-propan-2-ylindazole
2-(1-Methylethyl)-5-nitro-2H-indazole化学式
CAS
——
化学式
C10H11N3O2
mdl
——
分子量
205.21
InChiKey
NIPPRKGSQUHQMO-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):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    63.6
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors
    申请人:Rodgers D. James
    公开号:US20070135461A1
    公开(公告)日:2007-06-14
    The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
    本发明提供了杂环取代的吡咯并[2,3-b]吡啶和杂环取代的吡咯并[2,3-b]嘧啶,可以调节雅努斯激酶的活性,并且在治疗与雅努斯激酶活性相关的疾病中具有用处,例如免疫相关疾病、皮肤疾病、髓增生性疾病、癌症和其他疾病。
  • HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS
    申请人:Rodgers James D.
    公开号:US20090181959A1
    公开(公告)日:2009-07-16
    The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
    本发明提供了杂环取代的吡咯并[2,3-b]吡啶和杂环取代的吡咯并[2,3-b]嘧啶,可调节Janus激酶的活性,并可用于治疗与Janus激酶活性相关的疾病,包括免疫相关疾病、皮肤疾病、髓系增生性疾病、癌症和其他疾病。
  • Heteroaryl Substituted Pyrrolo[2,3-B]Pyridines And Pyrrolo[2,3-B]Pyrimidines As Janus Kinase Inhibitors
    申请人:Rodgers James D.
    公开号:US20140018374A1
    公开(公告)日:2014-01-16
    The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
    本发明提供了杂环取代的吡咯[2,3-b]吡啶和杂环取代的吡咯[2,3-b]嘧啶,其调节Janus激酶的活性,并且在治疗与Janus激酶活性相关的疾病中具有用处,包括但不限于免疫相关性疾病、皮肤疾病、髓样增生性疾病、癌症和其他疾病。
  • Heteroaryl Substituted Pyrrolo[2,3-B] Pyridines And Pyrrolo[2,3-B] Pyrimidines As Janus Kinase Inhibitors
    申请人:Incyte Corporation
    公开号:US20140243360A1
    公开(公告)日:2014-08-28
    The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.
    本发明提供了杂环取代的吡咯[2,3-b]吡啶和杂环取代的吡咯[2,3-b]嘧啶,这些化合物可以调节Janus激酶的活性,适用于治疗与Janus激酶活性相关的疾病,例如免疫相关疾病、皮肤疾病、髓系增生性疾病、癌症和其他疾病。
  • US7598257B2
    申请人:——
    公开号:US7598257B2
    公开(公告)日:2009-10-06
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