合成具有抗腸病毒活性「二苯」及 「亞甲基二苯」與「阿昔洛韋」之共軛化合物; Synthesis of Benzhydryl– and Benzhydrylidene–Acyclovir Conjugates with Anti-enterovirus Activity

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/61406

Title:	合成具有抗腸病毒活性「二苯」及「亞甲基二苯」與「阿昔洛韋」之共軛化合物;Synthesis of Benzhydryl– and Benzhydrylidene–Acyclovir Conjugates with Anti-enterovirus Activity
Authors:	羅世偉;Lo,Shih-Wei
Contributors:	化學學系
Keywords:	阿昔洛韋;腸病毒;Acyclovir;enterovirus
Date:	2013-08-12
Issue Date:	2013-10-08 15:07:42 (UTC+8)
Publisher:	國立中央大學
Abstract:	病毒造成的疾病與死亡是人類必須面對的問題，其中以高變異性RNA病毒所造成的傷害最為嚴重，至今仍缺乏合適抗該等病毒藥物與疫苗。因此「歐盟第七架構計畫」中將「黃病毒科」、「微小核醣核酸」病毒科等RNA病毒列為優先研究目標，欲開發抑制此類RNA病毒的化合物。本實驗室參與「歐盟第七架構計畫」中名為SILVER之計畫，致力於先導藥物開發。胡紀如教授實驗室過去將有抗病毒活性之藥物以連接鍵在一起，發現藥物「去甲替林」與「阿昔洛韋」鍵結之化合物對腸病毒具有良好的抑制活性，因此本人採用類似的架構設計分子，使用結構類似於「去甲替林」的「二苯胺類」或「亞甲基二苯胺類」化合物與「阿昔洛韋」鍵結。合成的方法為將「二苯胺類」或「亞甲基二苯胺類」藉由「三光氣」從胺基反應成「異氰酸酯」，再與「阿昔洛韋」衍生物進行加成反應。本人利用「核磁共振光譜儀」、「高解析質譜儀」和「紅外線光譜儀」鑑定合成之共軛化合物結構，最後將保護基去除得到目標分子。其中共軛化合物21具有抑制「腸病毒71型」之活性，其EC50 = 23.7 μM。 Virus-related diseases pose a serious global treat to human health. In particular, RNA viruses lack effective drugs and vaccines, largely owing to the rapid mutation rate of such viruses. Therefore, the Seventh Framework Programme in the European Union has approved a project that focuses on drugs discovery towards Flaviviridae and Picornaviridae. Our laboratory participating in this program, referred to as SILVER, Our laboratory is devoting its efforts developing lead candidate. The laboratory of Professor Jih Ru Hwu has combined two antiviral activity-related drugs together. Based on those results, nortriptyline–acyclovir conjugates to inhibit of enterovirus replication activity, Correspondingly, this study use a similar architecture design to molecular structure. Our indicate that benzhydryl or benzhydrylidene is similar to nortriptyline, so we replaces "nortriptyline" with benzhydryl or benzhydrylidene. This study focuses on benzhydryl–acyclovir and benzhydrylidene–acyclovir conjugates as the target product, The synthetic method uses triphosgene react with amines, allowing for functional group from amine to isocyanate, and then reacting with acyclovir derivatives. The target structures are confirmed by nuclear magnetic resonance, high resolution mass spectrometers, and infrared spectroscopy. Finally, a protecting group is removed to achieve the final target. For the conjugated compound 21 which inhibits "EV71" activity, its EC50 = 23.7 μM.
Appears in Collections:	[Graduate Institute of Chemistry] Electronic Thesis & Dissertation

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