研究生: |
陳吉峰 GeeFong Chen |
---|---|
論文名稱: |
SARS冠狀病毒蛋白酶抑制劑之開發與合成 Synthesis of SARS Coronavirus Main Protease Inhibitors as anti-SARS Therapeutic Agents |
指導教授: |
陳家俊
Chen, Chia-Chun |
學位類別: |
碩士 Master |
系所名稱: |
化學系 Department of Chemistry |
論文出版年: | 2004 |
畢業學年度: | 92 |
語文別: | 中文 |
論文頁數: | 58 |
中文關鍵詞: | 嚴重呼吸道症候群 |
英文關鍵詞: | Severe Acute Respiratory Syndrome |
論文種類: | 學術論文 |
相關次數: | 點閱:188 下載:15 |
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嚴重呼吸道症候群 (Severe Acute Respiratory Syndrome,SARS)是由感染性SARS冠狀病毒所引起的事件,在瞭解SARS冠狀病毒蛋白酶在生物體內的作用機制,期待能發展出SARS冠狀病毒蛋白酶的抑制劑。本論文使用Passerini反應為中心反應,快速地合成五個不同的SARS-CoV Mpro抑制劑核心結構,接著合成衍生出800個分子,利用這樣的分子庫,進行SARS抑制劑活性的篩選,試圖找出效果佳的抑制劑。在本合成的5個系列中,發現數個抑制活性IC50小於10 μΜ的分子,其中在系列4中,化合物35-B8及35-B5的IC50值分別為0.9、1.4,為分子庫中最佳的兩個可能抑制分子,希望利用這兩個分子作為核心結構,在C端衍生出不同的分子進行篩選,發展出更有效的抑制劑。
SARS (Severe Acute Respiratory Syndrome) is an infectious disease caused by a novel human coronavirus. SARS-CoV Mpro is a crucial protease in the virus’s replication cycle. By a understanding of SARS-CoV Mpro catalysis and a full substrate specificity spectrum for SARS-CoV Mpro, we hope to design and synthesize inhibitors against SARS. We applied the Passerini reaction to form five α-hydroxyl amide core structures and followed by formation of another amide bond to generate five α-hydroxyl amide libraries. Eight hundred compounds were synthesized and their activities against SARS-CoV Mpro were screened. Few compounds of the library members show their IC50 less than 10 μΜ. In the fourth series, we’ve found that compounds 35-B8 and 35-B5 showed strong inhibition (IC50 = 0.9、1.4μΜ) for SARS main protease. Then use compounds 35-B8 and 35-B5 as cores, its C-terminal can be further modified by amide or ester bond formation to yield new libraries. By means of this approach, the best SARS-CoV Mpro inhibitors were screened and obtained.
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