4.7 Article

Anti-HBV and cytotoxic activities of pyranocoumarin derivatives

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 17, Issue 16, Pages 6137-6143

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2008.12.007

Keywords

Pyranocoumarin derivatives; Anti-HBV; Cytotoxic

Funding

  1. National Science Council, Taiwan
  2. Republic of China [NSC94-2113-M006-008]
  3. NIH [CA-17625]

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Four natural pyranocoumarins clausenidin (1), nordentatin (2), clausarin (3), and xanthoxyletin (4) were isolated from the medicinal plant Clausena excavata. Recently, we found that 1 and 2 suppressed hepatitis B virus surface antigen in HepA2 cells, and in addition, 1-3 showed cytotoxic activity against four human cancer cell lines (A549, MCF7, KB, and KB-VIN). To explore the SAR of 1-4, 17 pyranocoumarin analogues (5-21) were designed and synthesized. Among these analogues, 5 and 10 were the most potent against hepatitis B virus with EC50 values of 1.14 and 1.34 mu M, respectively. The most interesting result in the cytotoxicity assay was the significant activity of 1, 5, and 6 against the multi-drug resistant cell line, KB-VIN, without activity against the KB cell line. These data suggest that these three compounds could be useful hits for developing MDR-inverse drugs. (C) 2009 Elsevier Ltd. All rights reserved.

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