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6-氨基-2-甲基-2H-1,4-苯并噻唑-3(4H)-酮 | 575485-66-4

中文名称
6-氨基-2-甲基-2H-1,4-苯并噻唑-3(4H)-酮
中文别名
——
英文名称
6-amino-2-methyl-2H-1,4-benzothiazin-3(4H)-one
英文别名
6-amino-2-methyl-4H-1,4-benzothiazin-3-one
6-氨基-2-甲基-2H-1,4-苯并噻唑-3(4H)-酮化学式
CAS
575485-66-4
化学式
C9H10N2OS
mdl
MFCD03001421
分子量
194.26
InChiKey
VMOAAHOOZGJEEB-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):
    1.1
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.222
  • 拓扑面积:
    80.4
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • 2,4-Pyrimidinediamine Compounds and Their Uses
    申请人:Singh Rajinder
    公开号:US20150266828A1
    公开(公告)日:2015-09-24
    The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.
    本发明提供了抑制IgE和/或IgG受体信号级联反应的2,4-嘧啶二胺化合物,该级联反应导致化学介质的释放,以及合成这些化合物的中介体和方法,以及在多种情况下使用这些化合物的方法,包括在治疗和预防由脱粒和其他由IgE和/或IgG受体信号级联反应激活引起的化学介质释放所表征、引起或相关的疾病。
  • 2, 4-pyrimidinediamine compounds and their uses
    申请人:Singh Rajinder
    公开号:US20050038243A1
    公开(公告)日:2005-02-17
    The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.
    本发明提供了抑制IgE和/或IgG受体信号级联,从而导致化学介质释放的2,4-嘧啶二胺化合物,以及合成这些化合物的中间体和方法,以及在多种情况下使用这些化合物的方法,包括在治疗和预防通过去颗粒化和其他由IgE和/或IgG受体信号级联激活的过程引起或与之相关的化学介质释放所表征的疾病中使用。
  • 2,4-Pyrimidinediamine compounds and their uses
    申请人:——
    公开号:US20040029902A1
    公开(公告)日:2004-02-12
    The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.
    本发明提供了抑制IgE和/或IgG受体信号级联引起化学介质释放的2,4-嘧啶二胺化合物,以及合成这些化合物的中间体和方法,以及在多种情境下使用这些化合物的方法,包括在治疗和预防由通过激活IgE和/或IgG受体信号级联引起的脱颗粒化和其他过程释放化学介质的疾病中。
  • 2,4-PYRIMIDINEDIAMINE COMPOUNDS AND THEIR USES
    申请人:Singh Rajinder
    公开号:US20070225321A1
    公开(公告)日:2007-09-27
    The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.
    本发明提供了能够抑制IgE和/或IgG受体信号级联反应从而导致化学介质释放的2,4-嘧啶二胺化合物,以及合成这些化合物的中间体和方法,以及在各种情况下使用这些化合物的方法,包括用于治疗和预防通过去颗粒化和其他通过激活IgE和/或IgG受体信号级联反应引起的化学介质释放所表征的,由化学介质引起或相关的疾病。
  • Heterocycle-Substituted Cyclic Urea Derivatives, Preparation Thereof And Pharmaceutical Use Thereof As Kinase Inhibitors
    申请人:Strobel Hartmut
    公开号:US20070259891A1
    公开(公告)日:2007-11-08
    The disclosure relates to compounds of formula (I): wherein Y, Y 1 , Yo, R1, R 2 , R 2 ′, p, R3, R 3 ′, A, B and Y 2 have the meanings given in the description, and to salts thereof, pharmaceutical compositions comprising said compounds and use thereof as protein kinase inhibitors.
    本披露涉及式(I)的化合物:其中Y,Y1,Yo,R1,R2,R2′,p,R3,R3′,A,B和Y2具有描述中给出的含义,以及其盐,包含该化合物的制药组合物以及其作为蛋白激酶抑制剂的用途。
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