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1-{4-[5-(2-Amino-thiazol-5-ylsulfanyl)-2,3-dimethyl-benzoyl]-piperazin-1-yl}-ethanone | 903568-49-0

中文名称
——
中文别名
——
英文名称
1-{4-[5-(2-Amino-thiazol-5-ylsulfanyl)-2,3-dimethyl-benzoyl]-piperazin-1-yl}-ethanone
英文别名
——
1-{4-[5-(2-Amino-thiazol-5-ylsulfanyl)-2,3-dimethyl-benzoyl]-piperazin-1-yl}-ethanone化学式
CAS
903568-49-0
化学式
C18H22N4O2S2
mdl
——
分子量
390.53
InChiKey
KLJGRSGWUUGNOY-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):
    2.8
  • 重原子数:
    26.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    79.53
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    1-{4-[5-(2-Amino-thiazol-5-ylsulfanyl)-2,3-dimethyl-benzoyl]-piperazin-1-yl}-ethanone4-二甲氨基苯甲酰氯吡啶 作用下, 以 二氯甲烷 为溶剂, 生成 N-[5-[[3-[(4-Acetylpiperazin-1-yl)carbonyl]-4,5-dimethylphenyl]thio]thiazol-2-yl]-4-(N,N-dimethylamino)benzamide
    参考文献:
    名称:
    Discovery and SAR of 2-amino-5-(thioaryl)thiazoles as potent and selective Itk inhibitors
    摘要:
    A series of structurally novel aminothiazole based small molecule inhibitors of Itk were prepared to elucidate their structure-activity relationships (SARs), selectivity, and cell activity in inhibiting IL-2 secretion in a Jurkat T-cell assay. Compound 3 is identified as a potent and selective Itk inhibitor which inhibits anti-TCR antibody induced IL-2 production in mice in vivo and was previously reported to reduce lung inflammation in a mouse model of ovalbumin induced allergy/asthma. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.04.060
  • 作为产物:
    参考文献:
    名称:
    Discovery and SAR of 2-amino-5-(thioaryl)thiazoles as potent and selective Itk inhibitors
    摘要:
    A series of structurally novel aminothiazole based small molecule inhibitors of Itk were prepared to elucidate their structure-activity relationships (SARs), selectivity, and cell activity in inhibiting IL-2 secretion in a Jurkat T-cell assay. Compound 3 is identified as a potent and selective Itk inhibitor which inhibits anti-TCR antibody induced IL-2 production in mice in vivo and was previously reported to reduce lung inflammation in a mouse model of ovalbumin induced allergy/asthma. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.04.060
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