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1H-Pyrazole-4-carboxaldehyde,5-[(2-furanylmethyl)thio]-1-phenyl-3-(trifluoromethyl)- | 929634-72-0

中文名称
——
中文别名
——
英文名称
1H-Pyrazole-4-carboxaldehyde,5-[(2-furanylmethyl)thio]-1-phenyl-3-(trifluoromethyl)-
英文别名
——
1H-Pyrazole-4-carboxaldehyde,5-[(2-furanylmethyl)thio]-1-phenyl-3-(trifluoromethyl)-化学式
CAS
929634-72-0
化学式
C16H11F3N2O2S
mdl
——
分子量
352.337
InChiKey
UYVRAQGUCVLYSL-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

物化性质

  • 沸点:
    451.6±45.0 °C(Predicted)
  • 密度:
    1.39±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.59
  • 重原子数:
    24.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    48.03
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    1H-Pyrazole-4-carboxaldehyde,5-[(2-furanylmethyl)thio]-1-phenyl-3-(trifluoromethyl)-二氢吡啶溶剂黄146β-丙氨酸 作用下, 以 甲苯 为溶剂, 反应 12.0h, 生成 5-[[5-(Furan-2-ylmethylsulfanyl)-1-phenyl-3-(trifluoromethyl)pyrazol-4-yl]methyl]-2-sulfanylidene-1,3-thiazolidin-4-one
    参考文献:
    名称:
    5-((1H-Pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5
    摘要:
    A series of 5-((1H-pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5 (aggrecanase-2) is described. These compounds show mu M functional inhibition of ADAMTS-5, and represent a new class of agents with the potential of inhibiting degradation of aggrecan, a major component of cartilage which is lost in osteoporosis. Compound 12 is noteworthy in that it has an ADAMTS-5 IC50: 1.1 mu M and shows > 40-fold functional selectivity over ADAMTS-4 (aggrecanase-1). (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.12.020
  • 作为产物:
    参考文献:
    名称:
    5-((1H-Pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5
    摘要:
    A series of 5-((1H-pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one inhibitors of ADAMTS-5 (aggrecanase-2) is described. These compounds show mu M functional inhibition of ADAMTS-5, and represent a new class of agents with the potential of inhibiting degradation of aggrecan, a major component of cartilage which is lost in osteoporosis. Compound 12 is noteworthy in that it has an ADAMTS-5 IC50: 1.1 mu M and shows > 40-fold functional selectivity over ADAMTS-4 (aggrecanase-1). (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.12.020
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