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6-chloro-3-[4-(trifluoromethoxy)phenyl]imidazo[1,2-b]pyridazine | 923595-75-9

中文名称
——
中文别名
——
英文名称
6-chloro-3-[4-(trifluoromethoxy)phenyl]imidazo[1,2-b]pyridazine
英文别名
——
6-chloro-3-[4-(trifluoromethoxy)phenyl]imidazo[1,2-b]pyridazine化学式
CAS
923595-75-9
化学式
C13H7ClF3N3O
mdl
——
分子量
313.666
InChiKey
OJIYYFZQHFKFNN-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):
    4.1
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    39.4
  • 氢给体数:
    0
  • 氢受体数:
    6

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。
  • FUSED HETEROCYCLES AS LCK INHIBITORS
    申请人:Nakai Kazuo
    公开号:US20100216798A1
    公开(公告)日:2010-08-26
    There is provided fused heterocycles of imidazopyridazine or pyrazolopyrimidine derivative represented by the formula (I), which have excellent Lck inhibitory activity and are useful for a medicament particularly an immunosuppressive agent. [wherein one of Y and Z is C atom, and the other is N atom; —X— is —N(R 1 )— or the like, —R 1 represents hydrogen or the like, -A- represents bond or the like, —R 2 is cycloalkyl, aryl or the like, -E- is bond or the like, —R 3 is aryl, aromatic heterocycle or the like, —R 4 , —R 5 and —R 6 are the same or different, each being hydrogen or the like.]
    提供了一种公式(I)所表示的咪唑吡啶嗪或吡唑嘧啶生物的熔合杂环,其具有出色的Lck抑制活性,可用于药物,特别是免疫抑制剂。[其中Y和Z中的一个是碳原子,另一个是氮原子;—X—是—N(R1)—或类似物,—R1表示氢或类似物,-A-表示键或类似物,—R2是环烷基,芳基或类似物,-E-是键或类似物,—R3是芳基,芳香杂环或类似物,—R4,—R5和—R6相同或不同,每个都是氢或类似物。]
  • IMIDAZO[1,2-B]PYRIDAZINE AND PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
    申请人:Xu Yong
    公开号:US20120058997A1
    公开(公告)日:2012-03-08
    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。还公开了将其用于治疗癌症和其他Pim激酶相关疾病的组合物和方法。
  • US7750007B2
    申请人:——
    公开号:US7750007B2
    公开(公告)日:2010-07-06
  • [EN] IMIDAZO[1,2-B]PYRIDAZINE AND PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS<br/>[FR] DÉRIVÉS D'IMIDAZO[1,2-B]PYRIDAZINE ET DE PYRAZOLO[1,5-A]PYRIMIDINE ET UTILISATION DE CEUX-CI COMME INHIBITEURS DE PROTÉINES KINASES
    申请人:SUPERGEN INC
    公开号:WO2008058126A2
    公开(公告)日:2008-05-15
    [EN] 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.
    [FR] L'invention concerne des inhibiteurs de protéines kinases qui comprennent des composés d'imidazo[1,2-b]pyridazine et de pyrazolo[1,5-a]pyrimidine représentés par les structures (I) et (II) suivantes, ou un stéréo-isomère, un promédicament ou un sel pharmaceutiquement acceptable de ceux-ci. Dans la formule, R, R1, R2 et X sont tels que définis dans la demande. L'invention concerne aussi des compositions et des procédés d'utilisation de celles-ci dans le traitement du cancer et d'autres états pathologiques associés à une kinase Pim.
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