4.7 Article

Synthesis and biological evaluation of N-substituted benzo[c]phenanthrolines and benzo[c]phenanthrolinones as antiproliferative agents

期刊

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 46, 期 6, 页码 2117-2131

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2011.02.065

关键词

Benzo[c]phenanthrolines; Benzo[c]phenanthrolinones; Dialkylaminoalkyl side chains; Cytotoxicity; DNA interactions

资金

  1. Universite de Lille 2/Conseil Regional Nord/Pas-de-Calais
  2. Institut pour la Recherche sur le Cancer de Lille (IRCL)
  3. Ligue Nationale Contre le Cancer (Comite du Nord)

向作者/读者索取更多资源

Benzo[c]phenanthrolines and benzo[c]phenanthrolinones substituted by dialkylaminoalkyl side chains at position N5 and C6, respectively, were synthesised and their biological activity evaluated. They displayed interessant cytotoxicity associated with some DNA interactions. However, the low topoisomerase 1 affinity suggests that other cellular targets are responsible for the antiproliferative activity. (C) 2011 Elsevier Masson SAS. All rights reserved.

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