4.5 Article

Synthesis and antimultidrug resistance evaluation of icariin and its derivatives

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 19, 期 15, 页码 4237-4240

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2009.05.103

关键词

Icariin derivatives; Synthesis; Multidrug resistance reversal activity; P-Glycoprotein inhibitors

资金

  1. National Nature Science Foundation of China [20772159, 90813011, U0832005]
  2. NSFC/RGC [30731160006]

向作者/读者索取更多资源

A series of icariin derivatives were synthesized. Their multidrug resistance (MDR) reversal activities were evaluated by MTT assay and the results indicated that the derivatives were the potent modulators of MDR. It was showed that the derivatives significantly increased the intracellular accumulation of ADR in MCF-7/ADR cells compared with drug sensitive MCF-7 cells. The results of bi-directional assay and reverse transcription polymerase chain reaction (RT-PCR) assay showed that the derivatives had high inhibitory activity against P-gp efflux function and significantly down-regulated on the expression of P-gp. (C) 2009 Elsevier Ltd. All rights reserved.

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