4.7 Article

Search for MDR modulators: Design, syntheses and evaluations of N-substituted acridones for interactions with p-glycoprotein and Mg2+

期刊

BIOORGANIC & MEDICINAL CHEMISTRY
卷 17, 期 6, 页码 2423-2427

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2009.02.002

关键词

Multi drug resistance; p-Glycoprotein; Hybrid molecules; Acridone derivatives; Modulators

资金

  1. DST
  2. UGC
  3. CSIR New Delhi

向作者/读者索取更多资源

By combining the structural features of acridone based anti-cancer drugs (like amsacrine) and MDR modulator propafenone, acridones with hydroxyl amine chain at N-10 have been designed and synthesized. These molecules exhibit appreciable interactions with p-gp and Mg2+ indicating their suitability to modulate p-gp mediated multi drug resistance. (C) 2009 Elsevier Ltd. All rights reserved.

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