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4-溴-2-(4-硝基苯基)喹啉-8-羧酸甲酯 | 651311-55-6

中文名称
4-溴-2-(4-硝基苯基)喹啉-8-羧酸甲酯
中文别名
——
英文名称
methyl 2-(4'-nitrophenyl)-4-bromo-quinoline-8-carboxylate
英文别名
Methyl 4-bromo-2-(4-nitrophenyl)quinoline-8-carboxylate;methyl 4-bromo-2-(4-nitrophenyl)quinoline-8-carboxylate
4-溴-2-(4-硝基苯基)喹啉-8-羧酸甲酯化学式
CAS
651311-55-6
化学式
C17H11BrN2O4
mdl
——
分子量
387.189
InChiKey
YQUQAGRUOKXIOV-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):
    4.2
  • 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:
    85
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-溴-2-(4-硝基苯基)喹啉-8-羧酸甲酯 在 lithium hydroxide 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 51.0h, 生成 4-[4-(Allyloxycarbonylamino-methyl)-phenylamino]-2-(4-nitro-phenyl)-quinoline-8-carboxylic acid
    参考文献:
    名称:
    Peptide Quinoline Conjugates:  A New Class of RNA-Binding Molecules
    摘要:
    A synthesis of 4,8-disubstituted 2-phenylquinoline amino acids is reported with the incorporation of one example into a peptide by solid-phase synthesis. The phenylquinoline-containing peptide binds an RNA target with nanomolar affinity (K-D = 208 nM). The strategy can be used to prepare a variety of 2-substituted quinoline amino acids for alteration of affinity in intercalator peptides. Since quinolones represent an important class of antibacterials, these compounds may be useful in the discovery of new antibacterial agents.
    DOI:
    10.1021/ol036094+
  • 作为产物:
    参考文献:
    名称:
    Peptide Quinoline Conjugates:  A New Class of RNA-Binding Molecules
    摘要:
    A synthesis of 4,8-disubstituted 2-phenylquinoline amino acids is reported with the incorporation of one example into a peptide by solid-phase synthesis. The phenylquinoline-containing peptide binds an RNA target with nanomolar affinity (K-D = 208 nM). The strategy can be used to prepare a variety of 2-substituted quinoline amino acids for alteration of affinity in intercalator peptides. Since quinolones represent an important class of antibacterials, these compounds may be useful in the discovery of new antibacterial agents.
    DOI:
    10.1021/ol036094+
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文献信息

  • Peptide Quinoline Conjugates:  A New Class of RNA-Binding Molecules
    作者:Malathy Krishnamurthy、Barry D. Gooch、Peter A. Beal
    DOI:10.1021/ol036094+
    日期:2004.1.1
    A synthesis of 4,8-disubstituted 2-phenylquinoline amino acids is reported with the incorporation of one example into a peptide by solid-phase synthesis. The phenylquinoline-containing peptide binds an RNA target with nanomolar affinity (K-D = 208 nM). The strategy can be used to prepare a variety of 2-substituted quinoline amino acids for alteration of affinity in intercalator peptides. Since quinolones represent an important class of antibacterials, these compounds may be useful in the discovery of new antibacterial agents.
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