Chem. J. Chinese Universities

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Structure-activity Relationships of Inhibitor of Terpenoids in GABAA Receptor

REN Tian-Rui1*; ZHAO Bao-Feng1,2; HU Yuan-Dong3; CI Su-Qin1,2   

  1. 1. State Key Laboratory of Biochemical Engineering, Institute of Process
    Engineering, Chinese Academy of Sciences, Beijing 100080, China;
    2. The Graduate University of Chinese Academy of Sciences, Beijing 100039,
    China;
    3. Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China
  • Received:2005-06-22 Revised:1900-01-01 Online:2006-07-10 Published:2006-07-10
  • Contact: REN Tian-Rui

Abstract: A variety of terpenoids of plant origin such as anisatin, picrotoxinin and picrodendrins were shown to be noncompetitive antagonists of GABAA receptors. The results show the selectivity toward the insect receptor and thus represent new leads toward selective insecticides. Two pharmacophore models of rat and housefly′s GABAA receptors for terpenoids inhibitors were studied by DISCOtech methodology. Two pharmacophore models were verified by the study of the threedimensional quantitative structure and activity relationships, which gave two predictive CoMFA models with q2rat=0.713 and q2fly=0.738. According to these results, it was found that negatively charged particle of inhibitor contributed strongly to binding at the rat receptor but showed almost no contribution to the housefly receptor. So these findings will lay a foundation of finding leading compounds and give some guidance on synthesizing insecticides with selectivity activity.

Key words: Inhibitors of terpenoids, Insecticide, Pharmacophore model, GABAA receptor, Comparative molecular field analysis

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