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ethyl 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-hydroxybutyrate | 1146221-15-9

中文名称
——
中文别名
——
英文名称
ethyl 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-hydroxybutyrate
英文别名
Ethyl 4-(1,4-dioxonaphthalen-2-yl)-3-hydroxybutanoate
ethyl 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-hydroxybutyrate化学式
CAS
1146221-15-9
化学式
C16H16O5
mdl
——
分子量
288.3
InChiKey
LGLNPMGUGXBOEC-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):
    1.3
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    80.7
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    ethyl 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-hydroxybutyrate 在 palladium 10% on activated carbon 、 氢气 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成
    参考文献:
    名称:
    Pyranonaphthoquinone Lactones: A New Class of AKT Selective Kinase Inhibitors Alkylate a Regulatory Loop Cysteine
    摘要:
    The naturally occurring pyranonaphthoquinone (PNQ) antibiotic lactoquinomycin and related aglycones were found to be selective inhibitors of the serine-threonine kinase AKT. A set of synthetic PNQs were prepared and a minimum active feature set and preliminary SAR were determined, PNQ lactones inhibit the proliferation of human tumor cell lines containing constitutively activated AKT and show expected effects on cellular biomarkers. Biochemical data are presented supporting a proposed bioreductive alkylation mechanism of action.
    DOI:
    10.1021/jm900075g
  • 作为产物:
    描述:
    3-hydroxypentanedioic acid monoethyl ester1,4-萘醌 在 ammonium peroxydisulfate 、 silver nitrate 作用下, 以 乙腈 为溶剂, 以29%的产率得到ethyl 4-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-3-hydroxybutyrate
    参考文献:
    名称:
    Pyranonaphthoquinone Lactones: A New Class of AKT Selective Kinase Inhibitors Alkylate a Regulatory Loop Cysteine
    摘要:
    The naturally occurring pyranonaphthoquinone (PNQ) antibiotic lactoquinomycin and related aglycones were found to be selective inhibitors of the serine-threonine kinase AKT. A set of synthetic PNQs were prepared and a minimum active feature set and preliminary SAR were determined, PNQ lactones inhibit the proliferation of human tumor cell lines containing constitutively activated AKT and show expected effects on cellular biomarkers. Biochemical data are presented supporting a proposed bioreductive alkylation mechanism of action.
    DOI:
    10.1021/jm900075g
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文献信息

  • Pyranonaphthoquinone Lactones: A New Class of AKT Selective Kinase Inhibitors Alkylate a Regulatory Loop Cysteine
    作者:Edward J. Salaski、Girija Krishnamurthy、Wei-Dong Ding、Ker Yu、Shabana S. Insaf、Clark Eid、Jaechul Shim、Jeremy I. Levin、Keiko Tabei、Lourdes Toral-Barza、Wei-Guo Zhang、Leonard A. McDonald、Erick Honores、Cilien Hanna、Ayako Yamashita、Bernard Johnson、Zhong Li、Leif Laakso、Dennis Powell、Tarek S. Mansour
    DOI:10.1021/jm900075g
    日期:2009.4.23
    The naturally occurring pyranonaphthoquinone (PNQ) antibiotic lactoquinomycin and related aglycones were found to be selective inhibitors of the serine-threonine kinase AKT. A set of synthetic PNQs were prepared and a minimum active feature set and preliminary SAR were determined, PNQ lactones inhibit the proliferation of human tumor cell lines containing constitutively activated AKT and show expected effects on cellular biomarkers. Biochemical data are presented supporting a proposed bioreductive alkylation mechanism of action.
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