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2000
Volume 2, Issue 6
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

The present review concentrates on camptothecin (CPT) analogues, the most extensively studied topoisomerase I (topo I) inhibitors, and provides concise information on the structural features of human topo I enzyme, mechanisms of interaction of CPT with topo I, structure-activity relationship study of CPT analogues including the influence of lactone stability on antitumor activity, and recent updates of valuable CPT analogues.

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/content/journals/mrmc/10.2174/1389557023405530
2002-12-01
2025-09-05
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