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7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H)quinolone | 1006049-56-4

中文名称
——
中文别名
——
英文名称
7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H)quinolone
英文别名
7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H) quinolone;methyl 2-[7-amino-2-oxo-4-(trifluoromethyl)-1H-quinolin-3-yl]acetate
7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H)quinolone化学式
CAS
1006049-56-4
化学式
C13H11F3N2O3
mdl
——
分子量
300.237
InChiKey
YAVYYUXANSQSJU-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):
    0.9
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    81.4
  • 氢给体数:
    2
  • 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
  • 下游产品
    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:
    7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H)quinolone溶剂黄146N,N'-二环己基碳二亚胺三氟乙酸 、 sodium hydroxide 作用下, 以 四氢呋喃1,4-二氧六环甲醇二甲基亚砜 为溶剂, 反应 6.67h, 生成
    参考文献:
    名称:
    FLUOROPHORE CHELATED LANTHANIDE LUMINESCENT PROBES WITH IMPROVED QUANTUM EFFICIENCY
    摘要:
    这项发明涉及含有荧光物质的新型发光组合物,制备这些组合物的合成方法,这些组合物的高分子共轭物,以及在各种检测方法中使用这些组合物的用途。该发明还提供了包含这些组合物及其共轭物的试剂盒,用于上述检测方法。
    公开号:
    US20130202536A1
  • 作为产物:
    描述:
    1-ethyl 4-methyl 2-(2,2,2-trifluoroacetyl)succinate间苯二胺 反应 4.0h, 以260mg的产率得到7-amino-4-trifluoromethyl-3-carbomethoxymethyl-2(1H)quinolone
    参考文献:
    名称:
    Dual-sensitizer-containing luminescent compounds, conjugates, and uses thereof
    摘要:
    这项发明涉及含有两种荧光团(敏化剂)的新型发光物质组合,制备这些组合的合成方法,这些组合的高分子共轭物,以及这些组合及其共轭物在各种检测方法中的应用。该发明还提供了包含这些组合及其共轭物的试剂盒,用于上述检测方法。
    公开号:
    US09415111B2
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文献信息

  • Luminescent Probes for Ultrasensitive Detection of Nucleic Acids
    作者:Lev N. Krasnoperov、Salvatore A. E. Marras、Maxim Kozlov、Laura Wirpsza、Arkady Mustaev
    DOI:10.1021/bc900403n
    日期:2010.2.17
    Novel amino-reactive derivatives of lanthanide-based luminescent labels of enhanced brightness and metal retention were synthesized and used for the detection of cDNA oligonucleotides by molecular beacons. Time-resolved acquisition of the luminescent signal that occurs upon hybridization of the probe to the target enabled the avoidance of short-lived background fluorescence, markedly enhancing the sensitivity of detection, which was less than 1 pM. This value is about 50 to 100 times More sensitive than the level achieved with conventional fluorescence-based molecular beacons, and is 10 to 60 times more sensitive than previously reported for other lanthanide-based hybridization probes. These novel luminescent labels should significantly enhance the sensitivity of all type of nucleic acid hybridization probes, and could dramatically improve the detection limit of other biopolymers and small compounds that are used in a variety of biological applications.
  • New quinolone-based thiol-reactive lanthanide luminescent probes
    作者:Laura Wirpsza、Lev Krasnoperov、Arkady Mustaev
    DOI:10.1016/j.jphotochem.2012.12.008
    日期:2013.2
    Luminescent lanthanide ion complexes are distinguished by unique light emitting properties that enable both highly sensitive detection of lanthanide labels attached to biomolecules and contrast imaging of various micro objects (cells, nanoparticles, etc.). Previously, we synthesized amine-reactive cs124-based luminescent lanthanide chelates with improved brightness and metal retention. Here we report the synthesis of new thiol-reactive derivatives of the same compounds including bromoacetamido-, and maleimido-forms of cs124 and cs124CF(3) fluorophores. Maleimido-compounds displayed exceptional reactivity instantaneously coupling to thiols at physiological conditions at micromolar probes concentrations. Surprisingly, they displayed strong quenching by adjacent maleimido-group, which was completely eliminated after reaction with thiols, thereby enabling their simple detection by monitoring the light emission of the reaction mixture. This reaction can be used for hyper-sensitive determination of biologically important sulphydryl compounds (e.g. glutathione, co-enzyme A, etc.) in time-resolved mode. (C) 2013 Elsevier B.V. All rights reserved.
  • US9221759B2
    申请人:——
    公开号:US9221759B2
    公开(公告)日:2015-12-29
  • US9732378B2
    申请人:——
    公开号:US9732378B2
    公开(公告)日:2017-08-15
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