天然产物研究与开发 ›› 2018, Vol. 30 ›› Issue (增刊1): 141-145.

• 研究简报 • 上一篇    下一篇

脱氢枞基α-氨基膦酸酯的合成与抗病毒活性研究

罗云龙1,沈明贵1*,蔡照胜2,王丹1,商士斌1,宋湛谦1   

  1. 1中国林业科学研究院林产化学工业研究所 生物质化学利用国家工程实验室 国家林业局林产化学工程重点开放性实验室 江苏省生物质能源与材料重点实验室,南京 210042;2盐城工学院化学与生物工程学院,盐城 224051  
  • 出版日期:2018-07-31 发布日期:2018-07-31
  • 基金资助:

    国家自然科学基金青年基金项目(31500487),中国林业科学研究院中央级公益性科研院所基本科研业务费专项资金(CAFYBB2016QB014)

Synthesis and Antiviral Activity Evaluation of α-Aminophosphonate Derivatives Containing Dehydroabietic Group

LUO Yun-long1, SHEN Ming-gui1*, CAI Zhao-sheng2, WANG Dan1, SHANG Shi-bin1, SONG Zhan-qian1   

  1. 1Institute of Chemical Industry of Forest Products,CAF;National Engineering Lab.for Biomass Chemical Utilization;Key and Open Laboratory of Forest Chemical Engineering,SFA,Nanjing 210042,China;2School of Chemical and Biological Engineering,Yancheng Institute of Technology,Yancheng 224051,China
  • Online:2018-07-31 Published:2018-07-31

摘要: 以TiO2为催化剂,在无溶剂体系下,脱氢枞胺、芳香醛和亚磷酸二乙酯经过三组分一锅法,合成脱氢枞基α-氨基膦酸酯衍生物。通过FT-IR、MS、1H NMR表征了化合物结构。利用MTT比色法测试了这些化合物对人体单纯疱疹病毒I型(HSV-1)的体外抗病毒活性。数据显示,在脱氢枞酸骨架结构上引入α-氨基膦酸酯可以一定程度提升化合物的抗病毒活性;α-氨基膦酸酯中苯环上取代基团的差异对它们的抗病毒活性影响不大。

关键词: 松香;脱氢枞酸;&alpha, -氨基膦酸酯;抗病毒

Abstract: A facile one-pot synthesis of α-aminophosphonates is achieved by three-component condensation of dehydroabietylamine,aldehyde and diethyl phosphite using TiO2 as a catalyst under solvent-free condition.The compounds were characterized by FT-IR,MS and 1H NMR.The antiviral activity of these α-aminophosphonate derivatives was evaluated against the Herpes simplex virus type I (HSV-1) through the MTT method.Preliminary structure activity relationship analysis suggests that the introduction of α-aminophosphonate group into the skeleton of dehydroabietic acid improves the antiviral activity of the derivatives.On the other hand,substituents of the benzene ring on the α-aminophosphonate group have little influence on the antiviral activity of the derivatives.

Key words: Rosin, Dehydroabietylamine, α-aminophosphonate, antiviral  

中图分类号:  O621.3 Q961