Chinese Journal of Applied Chemistry ›› 2015, Vol. 32 ›› Issue (9): 987-993.DOI: 10.11944/j.issn.1000-0518.2015.09.150019

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Synthesis and Anti-tumor Activities of Arylamino-α-glucofuranose Derivatives

SUN Baolia,ZHANG Yalinga,WANG Lilia,ZHANG Xiquanb,GU Hongmeib,LI Baolina*()   

  1. aKey Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry,School of Chemistry and Chemical Engineering,Shaanxi Normal University,Xi'an 710062,China
    bChia Tai Tianqing Pharmaceutical Co.,Ltd.,Nanjing,210042,China
  • Received:2015-01-19 Accepted:2015-04-16 Published:2015-08-31 Online:2015-08-31
  • Contact: LI Baolin
  • Supported by:
    Supported by the National Natural Science Foundation of China(No.21272144)

Abstract:

Four novel 1,2-O-isopropylidene-5-arylamino-α-glucofuranose derivatives were prepared using 2-methyl-5-nitrobenzoicacid and 2-chloro-5-nitrobenzoic acid, respectively, as the starting materials by a synthetic route including chlorination of carboxylic acid, Friedel-Crafts acylation, reduction of carbonyl, reduction of nitro and reductive amination. The structures of intermediates and target compounds were characterized by IR, NMR and HRMS. The anti-tumor activities of target compounds on three kinds of cells were tested preliminarily by MTT method. The results indicate that the anti-tumor activitives of compound 1a1 is better than other three kinds of target compounds on three kinds of tumor cells, especially on A431(IC50:(6.54±1.34) μmol/L).

Key words: arylaminogluofuranose derivatives, synthesis, anti-tumor activity