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methyl (2R,4S,5R,6R)-5-acetamido-2-chloro-6-[(1S,2R)-2,3-diacetyloxy-1-methoxypropyl]-4-methoxyoxane-2-carboxylate | 1400692-83-2

中文名称
——
中文别名
——
英文名称
methyl (2R,4S,5R,6R)-5-acetamido-2-chloro-6-[(1S,2R)-2,3-diacetyloxy-1-methoxypropyl]-4-methoxyoxane-2-carboxylate
英文别名
——
methyl (2R,4S,5R,6R)-5-acetamido-2-chloro-6-[(1S,2R)-2,3-diacetyloxy-1-methoxypropyl]-4-methoxyoxane-2-carboxylate化学式
CAS
1400692-83-2
化学式
C18H28ClNO10
mdl
——
分子量
453.874
InChiKey
VLWRRFXEXDSEDR-AIVZJVSBSA-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

物化性质

  • 沸点:
    587.2±50.0 °C(Predicted)
  • 密度:
    1.28±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.2
  • 重原子数:
    30
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    136
  • 氢给体数:
    1
  • 氢受体数:
    10

反应信息

点击查看最新优质反应信息

文献信息

  • Detection of Enzymes, Viruses, and Bacteria Using Glucose Meters
    作者:Amrita Das、Xikai Cui、Vasanta Chivukula、Suri S. Iyer
    DOI:10.1021/acs.analchem.8b02960
    日期:2018.10.2
    We also demonstrate that glucose oxidase or glucose dehydrogenase is not required because the paracetamol gets oxidized directly on the electrode surface. This indicates that test strips without glucose oxidase or dehydrogenase can be used, and we can detect analytes in the presence of high levels of background glucose. We demonstrate this unique nature of the assay to detect paracetamol in simulated
    我们开发了创新的检测方法,可以快速检测酶。携带扑热息痛邻苯二酚的化合物暴露于其各自的酶时,会释放出扑热息痛邻苯二酚,可以使用标准血糖仪对其进行检测。该方法用于检测多种分析物,包括酶(例如β-半乳糖苷酶α-甘露糖苷酶)以及病原体(例如流感病毒,肺炎链球菌和大肠杆菌)迅速。所有分析物的检出限极低,并且与流感病毒在临床上相关。我们还证明,由于扑热息痛在电极表面直接被氧化,因此不需要葡萄糖氧化酶或葡萄糖脱氢酶。这表明可以使用没有葡萄糖氧化酶或脱氢酶的试纸,并且我们可以在存在高平背景葡萄糖的情况下检测分析物。我们证明了这种检测方法的独特性质,可在模拟尿液和绵羊血液中检测扑热息痛,而不会干扰内在葡萄糖,这表明血糖仪可用于检测无葡萄糖分析物而无背景葡萄糖干扰。
  • Synthesis of novel N-acetylneuraminic acid derivatives as substrates for rapid detection of influenza virus neuraminidase
    作者:Wei Yang、Xiaoyu Liu、Xiaoxia Peng、Pei Li、Tianxin Wang、Guihua Tai、X. James Li、Yifa Zhou
    DOI:10.1016/j.carres.2012.06.009
    日期:2012.10
    Two novel N-acetylneuraminic acid derivatives, luciferyl N-acetylneuraminic acid (1) and luciferyl 4,7-di-O-methyl-N-acetylneuraminic acid (2), were designed and synthesized as substrates for the rapid detection of influenza virus neuraminidase. The sensitivity and specificity of the assays with compound 1 or 2 as the substrate for detection of neuraminidases from influenza virus (H1N1 and H5N1) and bacteria (A. ureafaciens and C. perfringens) were evaluated. Compound 1 was sensitive to neuraminidases from both influenza virus and bacteria. Bioluminescent assays with this compound with H1N1 and H5N1 neuraminidases were approximately 20- and 16-fold more sensitive, respectively, than the fluorescent method with the commercial substrate 4-MUNANA. In contrast, compound 2 was only sensitive to the neuraminidases from influenza virus, showing approximately 10- and 8-fold greater sensitivity than 4-MUNANA for the detection of H1N1 and H5N1 neuraminidases, respectively. The data showed that compound 2 could be used in assays for detection of an influenza viral neuraminidase. (c) 2012 Elsevier Ltd. All rights reserved.
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