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[4-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-phenyl]-dimethylamine | 1025065-93-3

中文名称
——
中文别名
——
英文名称
[4-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-phenyl]-dimethylamine
英文别名
[4-(6-Chloro-imidazo[1,2-b]pyridazine-3-yl)-phenyl]-dimethylamine;4-(6-chloroimidazo[1,2-b]pyridazin-3-yl)-N,N-dimethylaniline
[4-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-phenyl]-dimethylamine化学式
CAS
1025065-93-3
化学式
C14H13ClN4
mdl
——
分子量
272.737
InChiKey
ASOUHKXZUUBWLJ-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):
    3.1
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    33.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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

点击查看最新优质反应信息

文献信息

  • IMIDAZO[1,2-beta]PYRIDAZINE AND PYRAZOLO[1,5-alpha]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
    申请人:Bearss David J.
    公开号:US20080261988A1
    公开(公告)日:2008-10-23
    The present invention provides protein kinase inhibitors comprising imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine compounds of the following structure (I) and (II): or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein R, R 1 , R 2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer and other Pim kinase-associated conditions are also disclosed.
    本发明提供了蛋白激酶抑制剂,包括以下结构(I)和(II)的咪唑[1,2-b]吡啶吡唑[1,5-a]嘧啶化合物或其立体异构体、前药或药物可接受的盐,其中R、R1、R2和X如本文所定义。还公开了使用这些抑制剂治疗癌症和其他Pim激酶相关疾病的组合物和方法。
  • Imidazo[1,2-beta]pyridazine and pyrazolo[1,5-alpha]pyrimidine derivatives and their use as protein kinase inhibitors
    申请人:SuperGen, Inc.
    公开号:US07750007B2
    公开(公告)日:2010-07-06
    The present invention provides protein kinase inhibitors comprising imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine compounds of the following structure (I) and (II): or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer and other Pim kinase-associated conditions are also disclosed.
    本发明提供了蛋白激酶抑制剂,包括以下结构的咪唑并[1,2-b]吡啶吡唑并[1,5-a]嘧啶化合物(I)和(II):或其立体异构体、前药或药学上可接受的盐,其中R、R1、R2和X如定义所述。还揭示了使用该抑制剂在治疗癌症和其他Pim激酶相关疾病中的组合物和方法。
  • IMIDAZO[1,2-B]PYRIDAZINE AND PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
    申请人:Bearss David J.
    公开号:US20110281863A1
    公开(公告)日:2011-11-17
    The present invention provides protein kinase inhibitors comprising imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine compounds of the following structure (I) and (II): or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein R, R 1 , R 2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer and other Pim kinase-associated conditions are also disclosed.
    本发明提供蛋白激酶抑制剂,包括以下结构(I)和(II)的咪唑并[1,2-b]吡啶吡唑并[1,5-a]嘧啶化合物的立体异构体、前药或药物可接受的盐,其中R、R1、R2和X如本文所定义。还公开了在治疗癌症和其他Pim激酶相关疾病中使用这些化合物的组合物和方法。
  • Imidazo[1,2-B]pyridazine and pyrazolo[1 .5-A]pyrimidine derivatives and their use as protein kinase inhibitors
    申请人:Bearss David J.
    公开号:US08710057B2
    公开(公告)日:2014-04-29
    The present invention provides protein kinase inhibitors comprising imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine compounds of the following structure (I) and (II): or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer and other Pim kinase-associated conditions are also disclosed.
    本发明提供了以下结构(I)和(II)的咪唑并[1,2-b]吡嗪吡唑并[1,5-a]嘧啶化合物的蛋白激酶抑制剂,或其立体异构体、前药或药物可接受盐,其中R,R1,R2和X如本文所定义。还公开了在治疗癌症和其他Pim激酶相关疾病中使用这些化合物的组合物和方法。
  • IMIDAZOÝ1,2-B¨PYRIDAZINE AND PYRAZOLOÝ1,5-A¨PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
    申请人:SuperGen, Inc.
    公开号:EP2086979A2
    公开(公告)日:2009-08-12
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