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投稿时间:2019-07-08
投稿时间:2019-07-08
中文摘要: 基于虫草素中的氨基稳定性问题,对其氨基修饰,并与磁性材料杂化。丙烯酰氯为酰化剂,三乙胺为缚酸剂,对虫草素进行衍生化反应,采用高分辨质谱、核磁共振波谱进行表征,合成新化合物N-丙烯酰虫草素,其与3-氨基丙基三乙氧基硅烷进行模板反应得到N-[1-氧代丙烷-3-(3-(三乙氧基硅基)丙基)氨基]虫草素,进而与氨基磁性材料(Fe3O4-NH2)发生aza-Michael反应,用x射线粉末衍射、磁滞回线、茚三酮比色法证明杂化成Fe3O4-NH2@N-丙烯酰虫草素。N-丙烯酰虫草素,既有抗菌性,又能与无机材料杂化,是一种潜在的活性中间体。
Abstract:Based on the stability of amino group in cordycepin,the amino group of cordycepin was modified and cordycepin was hybridized with magnetic materials.N-acryloyl cordycepin was a new compound,which was synthesized with acryloyl chloride as acylating agent,triethylamine as acid-binding agent,and it was characterized by high resolution mass spectrometry,nuclear magnetic resonance spectra,it reacted with 3-aminopropyl triethoxysilane in template reaction to obtain N-[1-oxopropanyl-3-(3-(triethoxysilyl)propyl)amino]cordycepin.Then,the aza-Michael reaction of N-acryloyl cordycepin with amino magnetic material(Fe3O4-NH2)occurs.The hybridization product was proved to be Fe3O4-NH2@N-acryloyl cordycepin by means of X-ray powder diffraction,magnetic moments and ninhydrin colorimetry.Thus,N-acryloyl cordycepin was potential active intermediate because of its antimicrobial activity,hybridization with inorganic materials capacity.
keywords: cordycepin acryloyl chloride N-acrylamide cordycepin aza-Michael reaction N-[1-oxopropanyl-3-(3-(triethoxysilyl)propyl)amino]cordycepin Fe3O4-NH2@N-acrylamide cordycepin antimicrobial activity
文章编号:202007002 中图分类号: 文献标志码:
基金项目:国家自然科学基金项目(21964017)
Author Name | Affiliation |
JIN Ying-jin,ZHANG Jing-dong,WANG Si-hong,LI Dong-hao |
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