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

6-(methylsulfonyl)-4-quinolinol | 1062589-79-0

中文名称
——
中文别名
——
英文名称
6-(methylsulfonyl)-4-quinolinol
英文别名
6-(methylsulfonyl)-quinolin-4-ol;6-methylsulfonyl-1H-quinolin-4-one
6-(methylsulfonyl)-4-quinolinol化学式
CAS
1062589-79-0
化学式
C10H9NO3S
mdl
——
分子量
223.252
InChiKey
JSPOBZWJRUHRND-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):
    -0.2
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    71.6
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • 作为反应物:
    参考文献:
    名称:
    Compounds and Methods of Treatment
    摘要:
    本文描述了一种作为Ret酪氨酸激酶抑制剂有用的衍生物。所述发明还包括使用相同物质治疗由不当的Ret酪氨酸激酶活性介导的疾病的方法。
    公开号:
    US20080234267A1
  • 作为产物:
    描述:
    4-氨基茴香硫醚oxone 、 sodium hydroxide 作用下, 以 甲醇二苯醚乙醇 为溶剂, 反应 81.0h, 生成 6-(methylsulfonyl)-4-quinolinol
    参考文献:
    名称:
    The Identification and Pharmacological Characterization of 6-(tert-Butylsulfonyl)-N-(5-fluoro-1H-indazol-3-yl)quinolin-4-amine (GSK583), a Highly Potent and Selective Inhibitor of RIP2 Kinase
    摘要:
    RIP2 kinase is a central component of the innate immune system and enables downstream signaling following activation of the pattern recognition receptors NOD1 and NOD2, leading to the production of inflammatory cytokines. Recently, several inhibitors of RIP2 kinase have been disclosed that have contributed to the fundamental understanding of the role of RIP2 in this pathway. However, because they lack either broad kinase selectivity or strong affinity for RIP2, these tools have only limited utility to assess the role of RIP2 in complex environments. We present, herein, the discovery and pharmacological characterization of GSK583, a next-generation RIP2 inhibitor possessing exquisite selectivity and potency. Having demonstrated the pharmacological precision of this tool compound, we report its use in elucidating the role of RIP2 kinase in a variety of in vitro, in vivo, and ex vivo experiments, further clarifying our understanding of the role of RIP2 in NOD1 and NOD2 mediated disease pathogenesis.
    DOI:
    10.1021/acs.jmedchem.6b00211
点击查看最新优质反应信息

文献信息

  • Compounds and Methods of Treatment
    申请人:LACKEY Karen Elizabeth
    公开号:US20080234267A1
    公开(公告)日:2008-09-25
    A derivative, which is useful as a ret kinase inhibitor is described herein. The described invention also includes methods of using the same in the treatment of diseases mediated by inappropriate ret kinase activity.
    本文描述了一种作为Ret酪氨酸激酶抑制剂有用的衍生物。所述发明还包括使用相同物质治疗由不当的Ret酪氨酸激酶活性介导的疾病的方法。
  • QUINOLYL AMINES AS KINASE INHIBITORS
    申请人:Charnley Adam Kenneth
    公开号:US20120041024A1
    公开(公告)日:2012-02-16
    Disclosed are compounds having the formula: wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined herein, and methods of making and using the same.
    揭示了具有下列化学式的化合物:其中R1、R2、R3、R4和R5如本文所定义,并提供了制备和使用这些化合物的方法。
  • AMINO-QUINOLINES AS KINASE INHIBITORS
    申请人:GlaxoSmithKline Intellectual Property Development Limited
    公开号:EP2566477B1
    公开(公告)日:2015-09-02
  • US20140256949A1
    申请人:——
    公开号:——
    公开(公告)日:——
  • COMPOUNDS AND METHODS OF TREATMENT
    申请人:ANGELL RICHARD MARTYN
    公开号:US20110053934A1
    公开(公告)日:2011-03-03
    A derivative, which is useful as a ret kinase inhibitor is described herein. The described invention also includes methods of using the same in the treatment of diseases mediated by inappropriate ret kinase activity.
查看更多