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1-(2-Chloropyridin-4-yl)prop-2-yn-1-one | 1519604-94-4

中文名称
——
中文别名
——
英文名称
1-(2-Chloropyridin-4-yl)prop-2-yn-1-one
英文别名
1-(2-chloropyridin-4-yl)prop-2-yn-1-one
1-(2-Chloropyridin-4-yl)prop-2-yn-1-one化学式
CAS
1519604-94-4
化学式
C8H4ClNO
mdl
——
分子量
165.579
InChiKey
UNGFTPGOAZMZRB-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
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-(2-Chloropyridin-4-yl)prop-2-yn-1-one四(三苯基膦)钯一氯化碘 、 sodium carbonate 作用下, 以 乙二醇二甲醚乙醇二氯甲烷 为溶剂, 反应 21.0h, 生成
    参考文献:
    名称:
    Synthesis and SAR of novel isoxazoles as potent c-jun N-terminal kinase (JNK) inhibitors
    摘要:
    The design and synthesis of isoxazole 3 is described, a potent JNK inhibitor with two fold selectivity over p38. Optimization of this scaffold led to compounds 27 and 28 which showed greatly improved selectivity over p38 by maintaining the JNK3 potency of compound 3. Extensive SAR studies will be described as well as preliminary in vivo data of the two lead compounds. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.11.052
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文献信息

  • Synthesis and SAR of novel isoxazoles as potent c-jun N-terminal kinase (JNK) inhibitors
    作者:Yuanjun He、Derek Duckett、Weimin Chen、Yuan Yuan Ling、Michael D. Cameron、Li Lin、Claudia H. Ruiz、Philip V. LoGrasso、Theodore M. Kamenecka、Marcel Koenig
    DOI:10.1016/j.bmcl.2013.11.052
    日期:2014.1
    The design and synthesis of isoxazole 3 is described, a potent JNK inhibitor with two fold selectivity over p38. Optimization of this scaffold led to compounds 27 and 28 which showed greatly improved selectivity over p38 by maintaining the JNK3 potency of compound 3. Extensive SAR studies will be described as well as preliminary in vivo data of the two lead compounds. (C) 2013 Elsevier Ltd. All rights reserved.
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