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6-(3-trifluoromethylbenzoyloxy)-2-oxo-2H-naphtho[1,8-bc]furan

中文名称
——
中文别名
——
英文名称
6-(3-trifluoromethylbenzoyloxy)-2-oxo-2H-naphtho[1,8-bc]furan
英文别名
(3-Oxo-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaen-9-yl) 3-(trifluoromethyl)benzoate;(3-oxo-2-oxatricyclo[6.3.1.04,12]dodeca-1(12),4,6,8,10-pentaen-9-yl) 3-(trifluoromethyl)benzoate
6-(3-trifluoromethylbenzoyloxy)-2-oxo-2H-naphtho[1,8-bc]furan化学式
CAS
——
化学式
C19H9F3O4
mdl
——
分子量
358.273
InChiKey
GYORDKXQWOSWJZ-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):
    5
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    7

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

  • 作为产物:
    描述:
    参考文献:
    名称:
    2′-Deoxyuridine 5′-Monophosphate Substrate Displacement in Thymidylate Synthase through 6-Hydroxy-2H-naphtho[1,8-bc]furan-2-one Derivatives
    摘要:
    Thymidylate synthase (TS) is a target for antifolate-based chemotherapies of microbial and human diseases. Here, ligand-based, synthetic, and X-ray crystallography studies led to the discovery of 6-(3-cyanobenzoyloxy)-2-oxo-2H-naphto[1,8-bc]furan, a novel inhibitor with a K-i, of 310 nM against Pneumocystis carinii TS. The X-ray ternary complex with Escherichia coli TS revealed, for the first time, displacement of the substrate toward the dimeric protein interface, thus providing new opportunities for further design of specific inhibitors of microbial pathogens.
    DOI:
    10.1021/jm4014086
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文献信息

  • 2′-Deoxyuridine 5′-Monophosphate Substrate Displacement in Thymidylate Synthase through 6-Hydroxy-2<i>H</i>-naphtho[1,8-<i>bc</i>]furan-2-one Derivatives
    作者:Stefania Ferrari、Samuele Calò、Rosalida Leone、Rosaria Luciani、Luca Costantino、Susan Sammak、Flavio Di Pisa、Cecilia Pozzi、Stefano Mangani、M. Paola Costi
    DOI:10.1021/jm4014086
    日期:2013.11.27
    Thymidylate synthase (TS) is a target for antifolate-based chemotherapies of microbial and human diseases. Here, ligand-based, synthetic, and X-ray crystallography studies led to the discovery of 6-(3-cyanobenzoyloxy)-2-oxo-2H-naphto[1,8-bc]furan, a novel inhibitor with a K-i, of 310 nM against Pneumocystis carinii TS. The X-ray ternary complex with Escherichia coli TS revealed, for the first time, displacement of the substrate toward the dimeric protein interface, thus providing new opportunities for further design of specific inhibitors of microbial pathogens.
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