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t-butyl (Z)-2-(2'-deoxy-2'-phthalimido-6'-azido-6'-deoxy-β-D-galactopyranosyloxy)-3-p-hydroxyphenyl-2-acrylate | 864070-77-9

中文名称
——
中文别名
——
英文名称
t-butyl (Z)-2-(2'-deoxy-2'-phthalimido-6'-azido-6'-deoxy-β-D-galactopyranosyloxy)-3-p-hydroxyphenyl-2-acrylate
英文别名
tert-butyl (Z)-2-[(2S,3R,4R,5R,6R)-6-(azidomethyl)-3-(1,3-dioxoisoindol-2-yl)-4,5-dihydroxyoxan-2-yl]oxy-3-(4-hydroxyphenyl)prop-2-enoate
t-butyl (Z)-2-(2'-deoxy-2'-phthalimido-6'-azido-6'-deoxy-β-D-galactopyranosyloxy)-3-p-hydroxyphenyl-2-acrylate化学式
CAS
864070-77-9
化学式
C27H28N4O9
mdl
——
分子量
552.541
InChiKey
CCAJLZOFOOAMQC-ZSMJMNQMSA-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):
    3.3
  • 重原子数:
    40
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    157
  • 氢给体数:
    3
  • 氢受体数:
    11

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Synthesis of Staudinger-type Molecular Probe for Catch-and-release Purification of the Binding Protein for Potassium Isolespedezate, a Leaf-closing Substance of Leguminous Plant
    作者:Tomohiko Fujii、Nobuki Kato、Izumi Iwakura、Yoshiyuki Manabe、Minoru Ueda
    DOI:10.1246/cl.2008.52
    日期:2008.1.5
    We synthesized azide-containing photoaffinity probe 1 based on the structure of potassium isolespedezate. This probe can be used for catch-and-release-mechanism purification of binding protein for 1: photo-crosslinking with 1 gave azide-labeled receptor which can be captured by phosphane-linked gel matrix by the Staudinger ligation. After washing the gel, the caught binding protein can be released by the reductive cleavage of disulfide bond in 1. This process can be used as a convenient method for the purification of binding protein for bioactive natural product.
    我们根据异双哌酸的结构合成了含叠氮化物的光亲和探针1。该探针可用于结合蛋白的捕获和释放机制纯化,与 1 个给定叠氮化物标记的受体进行 1: 光交联,该受体可通过 Staudinger 连接被烷连接的凝胶基质捕获。洗涤凝胶后,捕获的结合蛋白可通过1中二键的还原断裂而释放。该过程可作为纯化具有生物活性的天然产物的结合蛋白的便捷方法。
  • Nanometer-scale direct observation of the receptor for the leaf-movement factor in plant cell by a novel TEM probe
    作者:Yoshiyuki Manabe、Takanori Sugimoto、Tomoyuki Kawasaki、Minoru Ueda
    DOI:10.1016/j.tetlet.2006.12.128
    日期:2007.2
    Electron microscopy is a useful method for observing localization of some proteins in a cell. In this Letter, we report a nanometer-scale direct observation of the receptor for a bioactive substance of small molecular weight by using TEM (transmission electron microscopy). We developed a novel TEM probe compound (1) that is a modified leaf-movement factor with benzophenone as a photoaffinity group and FITC as an antigen that is recognized by a nano-gold bound anti-FITC antibody. By using probe 1, we revealed that the receptor for the leaf-movement factor of Cassia mimosoides is localized in the plasma membrane of the plant motor cell. (c) 2007 Elsevier Ltd. All rights reserved.
  • Detection of potential membrane receptor proteins concerning circadian rhythmic leaf movement of legumes using novel photoaffinity probe compounds
    作者:Takanori Sugimoto、Tomohiko Fujii、Yuusuke Idutu、Shosuke Yamamura、Minoru Ueda
    DOI:10.1016/j.tetlet.2003.10.150
    日期:2004.1
    Circadian rhythmic plant leaf movement, called nyctinasty, is controlled by a time-course change in the internal concentration of the leaf-movement factor in the plant body. We report that specific binding protein (210 and 108 kDa) for a leaf movement factor, potassium lespedezate, is contained in the plasma membrane of the plant motor cell. These proteins Would be potential receptors for leaf-movement factor to control the leaf movement. (C) 2003 Elsevier Ltd. All rights reserved.
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