Chemical Research in Chinese Universities ›› 2006, Vol. 22 ›› Issue (3): 356-359.

• Articles • Previous Articles     Next Articles

Design, Synthesis, and Activities of Novel Derivatives of Isophthalamide and Benzene-1,3-disulfonamide

LIU Xiu-jie1,3, WANG Song-qing2, ZHANG Jing1, ZHANG Feng-xia1, LI Gui-zhu1, WANG Bao-jie1, SHAO Ying-lu1, ZHANG Li-guang1, FANG Lin1, CHENG Mao-sheng1   

  1. 1. The College of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, P.R. China;

    2. The College of Pharmaceutical and Biotechnology, Tianjin University, Tianjin 300072, P.R. China;

    3. The School of Biology and Chemistry, Tianjin University of Technology, Tianjin 300191, P.R. China
  • Received:2005-03-18 Online:2006-06-24 Published:2011-08-06

Abstract: Based on the antiplatelet aggregation mechanism and the bioisosterism principle of the reference drug picotamide, thirteen novel derivatives of arylamide and arylsulfonamide were designed and prepared. The biological activities of these derivatives were investigated. The chemical structures of the target compounds were confirmed by 1H NMR and IR. The in vitro activities of antiplatelet aggregation of the thirteen target compounds were assessed by Born's method. Compounds 2b and 8h have significant antiplatelet aggregation activities, which are superior to the corresponding activity of Picotamide.

Key words: Thromboxane, Antiplatelet, Isophthalamide, Disulfonamide, Synthesis