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

4,5,6,7-四氢-1-甲基-7-氧代-1H-吲唑-3-羧酸乙酯 | 802541-13-5

中文名称
4,5,6,7-四氢-1-甲基-7-氧代-1H-吲唑-3-羧酸乙酯
中文别名
1H-吲唑-3羧酸-4,5,6,7-四氢-1-甲基-7-羰基乙酯
英文名称
ethyl 1-methyl-7-oxo-4,5,6,7-tetrahydro-1H-indazole-3-carboxylate
英文别名
ethyl 1-methyl-7-oxo-5,6-dihydro-4H-indazole-3-carboxylate
4,5,6,7-四氢-1-甲基-7-氧代-1H-吲唑-3-羧酸乙酯化学式
CAS
802541-13-5
化学式
C11H14N2O3
mdl
——
分子量
222.244
InChiKey
CYKSYDSDCBBLQG-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):
    1.2
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    61.2
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    室温且干燥

SDS

SDS:75e5741d721fe8016e7354ef75407747
查看

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    [EN] PYRAZOLO-QUINAZOLINE DERIVATIVES,PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
    [FR] DERIVES DE PYRAZOLO-QUINAZOLINE, PROCEDE DE PREPARATION ASSOCIE ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE KINASE
    摘要:
    公开了配方(Ia)或(Ib)中定义的吡唑喹唑啉衍生物及其药用盐,其制备方法以及包含它们的药物组合物;本发明的化合物可能在治疗中对与异常蛋白激酶活性相关的疾病,如癌症,具有用处。
    公开号:
    WO2004104007A1
  • 作为产物:
    参考文献:
    名称:
    吡唑并[4,3-h]喹唑啉类化合物及其用途
    摘要:
    本发明涉及一类如下通式I所示的吡唑并[4,3‑h]喹唑啉类衍生物及其用途,该类化合物具有抑制细胞周期蛋白依赖性酶家族(CDKs)中不同亚型例如CDK4/6的活性,为预防和治疗癌症、代谢与免疫疾病、心血管病以及神经性疾病提供新的手段。
    公开号:
    CN107383019B
点击查看最新优质反应信息

文献信息

  • Pyrazolo-Quinazoline Derivatives, Process for Their Preparation and Their Use as Kinase Inhibitors
    申请人:Traquandi Gabriella
    公开号:US20090124605A1
    公开(公告)日:2009-05-14
    Pyrazolo-quinazoline derivatives of formula (Ia) or (Ib) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.
    本发明公开了式(Ia)或(Ib)的吡唑喹唑啉生物及其药学上可接受的盐,以及其制备方法和包含它们的制药组合物;本发明的化合物在治疗与蛋白激酶活性失调有关的疾病,如癌症中可能有用。
  • Pyrazolo-quinazoline derivatives, process for their preparation and their use as kinase inhibitors
    申请人:Traquandi Gabriella
    公开号:US20070185143A1
    公开(公告)日:2007-08-09
    Pyrazolo-quinazoline derivatives of formula (Ia) or (Ib) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention maybe useful in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer”.
    本发明公开了公式(Ia)或(Ib)中定义的吡唑并[3,4-d]喹唑啉生物及其药学上可接受的盐,其制备方法和包含它们的制药组合物;本发明中的化合物可能在治疗中有用,用于治疗与蛋白激酶活性失调有关的疾病,如癌症。
  • SUBSTITUTED PYRAZOLO-QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
    申请人:Caruso Michele
    公开号:US20100216808A1
    公开(公告)日:2010-08-26
    Pyrazolo-quinazoline derivatives of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.
    本发明揭示了式(I)中所定义的吡唑喹唑啉生物及其药学上可接受的盐,以及它们的制备方法和包含它们的制药组合物;本发明中的化合物在治疗与蛋白激酶活性失调相关的疾病,如癌症中可能有用。
  • Substituted pyrazolo-quinazoline derivatives, process for their preparation and their use as kinase inhibitors
    申请人:Caruso Michele
    公开号:US08614220B2
    公开(公告)日:2013-12-24
    Pyrazolo-quinazoline derivatives of formula (I) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.
    本发明揭示了式(I)中定义的吡唑喹唑啉生物及其药学上可接受的盐,以及它们的制备方法和包含它们的制药组合物;本发明中的化合物可能在治疗与蛋白激酶活性失调有关的疾病(如癌症)中有用。
  • PYRAZOLO-QUINAZOLINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS
    申请人:Traquandi Gabriella
    公开号:US20130338148A1
    公开(公告)日:2013-12-19
    Pyrazolo-quinazoline derivatives of formula (Ia) or (Ib) as defined in the specification, and pharmaceutically acceptable salts thereof, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful, in therapy, in the treatment of diseases associated with a disregulated protein kinase activity, like cancer.
    本发明揭示了式(Ia)或(Ib)的吡唑喹唑啉生物及其药学上可接受的盐,以及它们的制备方法和包含它们的制药组合物;本发明的化合物可能在治疗与蛋白激酶活性失调相关的疾病,如癌症方面有用。
查看更多