Perspectives on Biologically Active Camptothecin Derivatives

Ying-Qian Liu(Lanzhou University), Wen-Qun Li(Lanzhou University), Susan L. Morris‐Natschke(University of North Carolina at Chapel Hill), Keduo Qian(University of North Carolina at Chapel Hill), Yang Liu(Lanzhou Jiaotong University), Gao-Xiang Zhu(Lanzhou University), Xiao-Bing Wu(Lanzhou University), An-Liang Chen(Zhejiang A & F University), Shao-Yong Zhang(Zhejiang A & F University), Xiang Nan(Lanzhou University), Kuo‐Hsiung Lee(University of North Carolina at Chapel Hill)
Medicinal Research Reviews
March 21, 2015
Cited by 204

Abstract

Camptothecins (CPTs) are cytotoxic natural alkaloids that specifically target DNA topoisomerase I. Research on CPTs has undergone a significant evolution from the initial discovery of CPT in the late 1960s through the study of synthetic small-molecule derivatives to investigation of macromolecular constructs and formulations. Over the past years, intensive medicinal chemistry efforts have generated numerous CPT derivatives. Three derivatives, topotecan, irinotecan, and belotecan, are currently prescribed as anticancer drugs, and several related compounds are now in clinical trials. Interest in other biological effects, besides anticancer activity, of CPTs is also growing exponentially, as indicated by the large number of publications on the subject during the last decades. Therefore, the main focus of the present review is to provide an ample but condensed overview on various biological activities of CPT derivatives, in addition to continued up-to-date coverage of anticancer effects.


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