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1-hydroxy-N-[(4-nitrophenyl)methyl]naphthalene-2-carboxamide | 27179-77-7

中文名称
——
中文别名
——
英文名称
1-hydroxy-N-[(4-nitrophenyl)methyl]naphthalene-2-carboxamide
英文别名
——
1-hydroxy-N-[(4-nitrophenyl)methyl]naphthalene-2-carboxamide化学式
CAS
27179-77-7
化学式
C18H14N2O4
mdl
——
分子量
322.32
InChiKey
GXQSALKDCSGKSP-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):
    4
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    95.2
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    Naphthalene carboxamides as inhibitors of human cytomegalovirus DNA polymerase
    摘要:
    ortho-Hydroxynaphthalene carboxamides have been identified as inhibitors of HCMV DNA polymerase. SAR investigations have demonstrated that both the amide and hydroxy functionalities are required for activity. Substitution on the naphthalene ring has led to inhibitors with submicromolar IC(50)s against HCMV polymerase. These compounds have been found to be >100-fold selective for inhibition of HCMV polymerase versus human alpha polymerase and display antiviral activity in a cell-based plaque reduction assay. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00402-9
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文献信息

  • Naphthalene carboxamides as inhibitors of human cytomegalovirus DNA polymerase
    作者:Valerie A Vaillancourt、Michele M Cudahy、Sandra A Staley、Roger J Brideau、Steven J Conrad、Mary L Knechtel、Nancee L Oien、Janet L Wieber、Yoshihiko Yagi、Michael W Wathen
    DOI:10.1016/s0960-894x(00)00402-9
    日期:2000.9
    ortho-Hydroxynaphthalene carboxamides have been identified as inhibitors of HCMV DNA polymerase. SAR investigations have demonstrated that both the amide and hydroxy functionalities are required for activity. Substitution on the naphthalene ring has led to inhibitors with submicromolar IC(50)s against HCMV polymerase. These compounds have been found to be >100-fold selective for inhibition of HCMV polymerase versus human alpha polymerase and display antiviral activity in a cell-based plaque reduction assay. (C) 2000 Elsevier Science Ltd. All rights reserved.
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