中大機構典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/94747
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 80990/80990 (100%)
造访人次 : 41635490      在线人数 : 1408
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/94747


    题名: 選擇性標記含胍基化合物的化學探針分子;Selective Chemical Probes for Labelling of Guanidine-bearing Molecule傑
    作者: 林俊甫;Lin, Jun-Fu
    贡献者: 化學學系
    关键词: ;精胺酸;光開關;1,2-雙酮;轉譯後修飾;標定;guanidine;arginine;photoswitch;1,2-diketone;post-translational modification;labelling
    日期: 2024-08-20
    上传时间: 2024-10-09 15:27:43 (UTC+8)
    出版者: 國立中央大學
    摘要: 胍基是一種強鹼性的含氮有機化合物官能基,通常在生理條件下帶有正電荷,能形成電荷-電荷作用力及多重氫鍵。精胺酸側鏈上的胍基是典型例子,精胺酸在蛋白質後修飾轉譯功能中發揮關鍵作用,如瓜胺酸化(citrullination)和甲基化(methylation)已被揭露與多種疾病生成有關,如類風濕性關節炎、狼瘡、朊病毒病和阿茲海默症等,近期科學家對於蛋白質上精胺酸後修飾對標靶蛋白的調節作用研究不遺餘力。在本篇論文中,我們合成一系列八環1,2-雙酮的衍生物,可以選擇性與胍基化合物或脲基化合物進行脫水重排反應,形成五七螺環的穩定產物;另一方面,我們設計製備具有偶氮官能基的八環1,2-雙酮化合物,透過照光預期可活化八環1,2-雙酮化合物與胍基的反應性,將使八環1,2-雙酮化合物成為更有應用性對含胍基化合物標定的化學探針工具。;Guanidine is a strongly alkaline nitrogen-containing organic compound that typically has a positive charge under physiological conditions. It is capable of forming charge–charge interactions and multiple hydrogen bonds. The guanidino group on the side chain of arginine is a typical example. Arginine plays a crucial role in the post-translational modification of proteins, such as citrullination and methylation, which have been linked to various diseases, such as rheumatoid arthritis, lupus, prion diseases and Alzheimer′s disease. Recently, scientists have dedicated significant efforts to studying the regulatory effects of post-translational modifications (PTMs) of arginine on proteins. In this thesis, we synthesized a series of dibenzocyclooctendione derivatives capable of undergoing condensation and rearrangement reactions with guanidine- or urea-bearing compounds to form a stable product with 5,7-spiroring. On the other hand, we also designed and synthesized octahydro-1,2-quinoline compounds with azo functional groups as chemical probes. These probes are expected to regulate the reactivity of the probe with guanidino and urea groups by controlling the E/Z isomerization of the photoswtich. This design aims to make them more versatile chemical probe tools for selectively labeling guanidine- and urea-containing compounds.
    显示于类别:[化學研究所] 博碩士論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML25检视/开启


    在NCUIR中所有的数据项都受到原著作权保护.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明