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Aethyl-p-carboxybenzoylpyruvat | 40155-55-3

中文名称
——
中文别名
——
英文名称
Aethyl-p-carboxybenzoylpyruvat
英文别名
1-Ethyl 4-carboxy-I+/-,I(3)-dioxobenzenebutanoate;4-(4-ethoxy-3,4-dioxobutanoyl)benzoic acid
Aethyl-p-carboxybenzoylpyruvat化学式
CAS
40155-55-3
化学式
C13H12O6
mdl
——
分子量
264.235
InChiKey
ZNTAYZAKAGLNAI-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):
    1.09
  • 重原子数:
    19.0
  • 可旋转键数:
    6.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    97.74
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    Aethyl-p-carboxybenzoylpyruvat 在 lithium hydroxide 作用下, 以 乙醇 为溶剂, 反应 0.67h, 生成 5-(4-Carboxyphenyl)-1-(3,4-dichlorophenyl)pyrazole-3-carboxylic acid
    参考文献:
    名称:
    Diphenylpyrazoles as Replication Protein A Inhibitors
    摘要:
    Replication Protein A is the primary eukaryotic ssDNA binding protein that has a central role in initiating the cellular response to DNA damage. RPA recruits multiple proteins to sites of DNA damage via the N-terminal domain of the 70 kDa subunit (RPA70N). Here we describe the optimization of a diphenylpyrazole carboxylic acid series of inhibitors of these RPA-protein interactions. We evaluated substituents on the aromatic rings as well as the type and geometry of the linkers used to combine fragments, ultimately leading to submicromolar inhibitors of RPA70N protein-protein interactions.
    DOI:
    10.1021/ml5003629
  • 作为产物:
    描述:
    4-乙酰基苯甲酸草酸二乙酯sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 0.33h, 生成 Aethyl-p-carboxybenzoylpyruvat
    参考文献:
    名称:
    Diphenylpyrazoles as Replication Protein A Inhibitors
    摘要:
    Replication Protein A is the primary eukaryotic ssDNA binding protein that has a central role in initiating the cellular response to DNA damage. RPA recruits multiple proteins to sites of DNA damage via the N-terminal domain of the 70 kDa subunit (RPA70N). Here we describe the optimization of a diphenylpyrazole carboxylic acid series of inhibitors of these RPA-protein interactions. We evaluated substituents on the aromatic rings as well as the type and geometry of the linkers used to combine fragments, ultimately leading to submicromolar inhibitors of RPA70N protein-protein interactions.
    DOI:
    10.1021/ml5003629
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