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N-methylmorpholinium 5-(anilinocarbonyl)-3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-1,4-dihydropyridine-2-thiolate | 1448816-20-3

中文名称
——
中文别名
——
英文名称
N-methylmorpholinium 5-(anilinocarbonyl)-3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-1,4-dihydropyridine-2-thiolate
英文别名
——
N-methylmorpholinium 5-(anilinocarbonyl)-3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-1,4-dihydropyridine-2-thiolate化学式
CAS
1448816-20-3
化学式
C5H11NO*C21H19N3O3S
mdl
——
分子量
494.615
InChiKey
JZPRKQYYGVLZIE-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):
    3.61
  • 重原子数:
    35.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    106.85
  • 氢给体数:
    4.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    N-methylmorpholinium 5-(anilinocarbonyl)-3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-1,4-dihydropyridine-2-thiolate2-氯-n-(4-乙基苯基)乙酰胺 在 potassium hydroxide 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以61%的产率得到5-cyano-6-({2-[(4-ethylphenyl)amino]-2-oxoethyl}thio)-4-(4-hydroxy-3-methoxyphenyl)-2-methyl-N-phenyl-1,4-dihydropyridine-3-carboxamide
    参考文献:
    名称:
    Inhibitors of Tick-Borne Flavivirus Reproduction from Structure-Based Virtual Screening
    摘要:
    Flaviviruses form a large family of enveloped viruses affecting millions of people over the world. To date, no specific therapy was suggested for the infected people, making the treatment exclusively symptomatic. Several attempts were performed earlier for the design of fusion inhibitors for mosquito-borne flaviviruses, whereas for the tick-borne flaviviruses such design had not been performed. We have constructed homology models of envelope glycoproteins of tick-transmitted flaviviruses with the detergent binding pocket in the open state. Molecular docking of substituted 1,4-dihydropyridines and pyrido[2,1-b][1,3,5]-thiadiazines was made against these models, and 89 hits were selected for the in vitro experimental evaluation. Seventeen compounds showed significant inhibition against tick-borne encephalitis virus, Powassan virus, or Omsk hemorrhagic fever virus in the 50% plaque reduction test in PEK. cells. These compounds identified through rational design are the first ones possessing reproduction inhibition activity against tick-borne flaviviruses.
    DOI:
    10.1021/ml400226s
  • 作为产物:
    参考文献:
    名称:
    Inhibitors of Tick-Borne Flavivirus Reproduction from Structure-Based Virtual Screening
    摘要:
    Flaviviruses form a large family of enveloped viruses affecting millions of people over the world. To date, no specific therapy was suggested for the infected people, making the treatment exclusively symptomatic. Several attempts were performed earlier for the design of fusion inhibitors for mosquito-borne flaviviruses, whereas for the tick-borne flaviviruses such design had not been performed. We have constructed homology models of envelope glycoproteins of tick-transmitted flaviviruses with the detergent binding pocket in the open state. Molecular docking of substituted 1,4-dihydropyridines and pyrido[2,1-b][1,3,5]-thiadiazines was made against these models, and 89 hits were selected for the in vitro experimental evaluation. Seventeen compounds showed significant inhibition against tick-borne encephalitis virus, Powassan virus, or Omsk hemorrhagic fever virus in the 50% plaque reduction test in PEK. cells. These compounds identified through rational design are the first ones possessing reproduction inhibition activity against tick-borne flaviviruses.
    DOI:
    10.1021/ml400226s
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