An Overview on the Development of New Potentially Active Camptothecin Analogs Against Cancer

Author(s): Eliza de Lucas Chazin, Raisa da Rocha Reis, Walcimar Trindade Vellasco Junior, Lucas Fajardo Elmor Moor, Thatyana Rocha Alves Vasconcelos.

Journal Name: Mini-Reviews in Medicinal Chemistry

Volume 14 , Issue 12 , 2014

Become EABM
Become Reviewer

Abstract:

Camptothecin (CPT) and its derivatives comprise an important group of heterocyclic compounds that are well recognized for their anticancer activities. Efforts have been made over the years aiming to develop new CPT analogs with better clinical efficacy, improved pharmacokinetic profile and lower toxicity. First generation of analogs, irinotecan (CPT-11) and topotecan (TPT) was approved for use by FDA in 1996 for the treatment of colorectal (CPT-11) and cervical, ovarian and small lung cancers (TPT). Other analogs of CPT are currently in different phases of clinical trials. As CPT represents an important lead compound in the field of antitumor- research, in this review we will highlight some recent discoveries (2008-2013) on the development of novel camptothecin-based compounds as potential anticancer agents.

Keywords: Camptothecin, cancer, drugs, homocamptothecin, irinotecan, topoisomerase inhibitors, topotecan.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 14
ISSUE: 12
Year: 2014
Page: [953 - 962]
Pages: 10
DOI: 10.2174/1389557514666141029233037
Price: $58

Article Metrics

PDF: 44