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3-(4,6-Dimethylpyridin-2-yl)-2-(2-fluoro-6-methoxyphenyl)-1,3-thiazolidin-4-one

中文名称
——
中文别名
——
英文名称
3-(4,6-Dimethylpyridin-2-yl)-2-(2-fluoro-6-methoxyphenyl)-1,3-thiazolidin-4-one
英文别名
——
3-(4,6-Dimethylpyridin-2-yl)-2-(2-fluoro-6-methoxyphenyl)-1,3-thiazolidin-4-one化学式
CAS
——
化学式
C17H17FN2O2S
mdl
——
分子量
332.399
InChiKey
WARRVPIVVUTEQB-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):
    3.5
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    67.7
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-氨基-4,6-二甲基吡啶巯基乙酸2-氟-6-甲氧基苯甲醛甲苯 为溶剂, 反应 48.0h, 以33%的产率得到3-(4,6-Dimethylpyridin-2-yl)-2-(2-fluoro-6-methoxyphenyl)-1,3-thiazolidin-4-one
    参考文献:
    名称:
    Synthesis of new 2,3-diaryl-1,3-thiazolidin-4-ones as anti-HIV agents
    摘要:
    Several 2,3-diaryl-1,3-thiazolidin-4-ones were synthesized and evaluated as anti-HIV agents. The results of the in vitro tests showed that some of them were highly effective inhibitors of HIV-1 replication at 30-50 nM concentrations with minimal cytotoxicity, thereby acting as non-nucleoside HIV-1 reverse transcriptase inhibitors (NNRTIs).
    DOI:
    10.1016/j.farmac.2003.09.001
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文献信息

  • Synthesis of new 2,3-diaryl-1,3-thiazolidin-4-ones as anti-HIV agents
    作者:Angela Rao、Jan Balzarini、Anna Carbone、Alba Chimirri、Erik De Clercq、Anna Maria Monforte、Pietro Monforte、Christophe Pannecouque、Maria Zappalà
    DOI:10.1016/j.farmac.2003.09.001
    日期:2004.1
    Several 2,3-diaryl-1,3-thiazolidin-4-ones were synthesized and evaluated as anti-HIV agents. The results of the in vitro tests showed that some of them were highly effective inhibitors of HIV-1 replication at 30-50 nM concentrations with minimal cytotoxicity, thereby acting as non-nucleoside HIV-1 reverse transcriptase inhibitors (NNRTIs).
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