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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2010, Vol. 15 ›› Issue (7): 814-820.

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Research advance on P-glycoprotein inhibitors and the structure-activity relationship

WEN Xiao-zhou, ZHOU Fang, WU Xiao-lan, WANG Guang-ji   

  1. Key Laboratory of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University Nanjing 210009, Jiangsu, China
  • Received:2010-04-07 Revised:2010-05-11 Online:2010-07-26 Published:2020-09-15

Abstract: P-glycoprotein (P-gp) is an important ATP-dependent transmembrane transporter, which can pump out a large number of structural and functional diverse compounds. P-gp plays a prominent role in physiological and pathological functions. It is not only crucial to drug disposition, but also one of the main causes of multidrug resistance (MDR). Therefore, developing P-gp inhibitors is significant to researches on modulation of drug pharmacokinetics and reversion of multidrug resistance. In this paper, we summarize studies on structure-activity relationship of P-gp inhibitors, which will give us important information for screening and synthesizing desirable P-gp inhibitors in the future.

Key words: P-glycoprotein, Multidrug resistance, Structure-activity relationship

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