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(2E,4E)-6-(4,6-dimethylpyrimidin-2-yl)sulfonyl-N-hydroxy-4-methylhepta-2,4-dienamide | 1265587-08-3

中文名称
——
中文别名
——
英文名称
(2E,4E)-6-(4,6-dimethylpyrimidin-2-yl)sulfonyl-N-hydroxy-4-methylhepta-2,4-dienamide
英文别名
——
(2E,4E)-6-(4,6-dimethylpyrimidin-2-yl)sulfonyl-N-hydroxy-4-methylhepta-2,4-dienamide化学式
CAS
1265587-08-3
化学式
C14H19N3O4S
mdl
——
分子量
325.389
InChiKey
HUYQPEKUALVXKZ-SBIWHPGTSA-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):
    1.3
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    118
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    ethyl (2E,4E)-6-((4,6-dimethylpyrimidin-2-yl)sulfonyl)-4-methylhepta-2,4-dienoate 在 盐酸羟胺 、 potassium hydroxide 作用下, 反应 8.0h, 生成 (2E,4E)-6-(4,6-dimethylpyrimidin-2-yl)sulfonyl-N-hydroxy-4-methylhepta-2,4-dienamide
    参考文献:
    名称:
    Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors
    摘要:
    A series of novel hydroxamic acid based histone deacetylases (HDAC) inhibitors with aryl ether and aryl sulfone residues at the terminus of a substituted, unsaturated 5-carbon spacer moiety have been synthesized for the first time and evaluated. Compounds with meta-and para-substitution on the aryl ring of ether hydroxamic acids 19c, 20c, 19e, 19f and 19g are potent HDAC inhibitors with activities at low nanomolar levels. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.11.006
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文献信息

  • Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors
    作者:Chittari Pabba、Brian T. Gregg、Douglas B. Kitchen、Zhen Jia Chen、Angela Judkins
    DOI:10.1016/j.bmcl.2010.11.006
    日期:2011.1
    A series of novel hydroxamic acid based histone deacetylases (HDAC) inhibitors with aryl ether and aryl sulfone residues at the terminus of a substituted, unsaturated 5-carbon spacer moiety have been synthesized for the first time and evaluated. Compounds with meta-and para-substitution on the aryl ring of ether hydroxamic acids 19c, 20c, 19e, 19f and 19g are potent HDAC inhibitors with activities at low nanomolar levels. (C) 2010 Elsevier Ltd. All rights reserved.
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