Synthesis and antitumor activity of sulfur-containing 9-anilinoacridines

Kun Ming Chen, Yuan Wan Sun, Yu Wei Tang, Zhong Yue Sun, Chul Hoon Kwon

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20 Scopus citations

Abstract

A series of sulfur-containing 9-anilinoacridines related to amsacrine were synthesized and evaluated for their anticancer potential. Among the compounds, both diol-containing compounds, 2a and 3, were the most cytotoxic of the sulfide series against V-79 cells in vitro (IC90 = 2.1 μM and 1.9 μM, respectively). Among the non-alkyl-substituted compounds (7-9), compounds with electron-donating substitution para to the sulfide (7 and 9) were more cytotoxic than the electron-withdrawing nitro-substituted compound 8. The limited SAR suggested the importance of hydroxyl functionality along with its location for the cytotoxicity in the series. A preliminary anticancer screening against P388 leukemia showed that 2a is highly active in vivo as well. Topoisomerase II inhibitory activity appeared to be involved in the cytotoxicity of compound 2a. Sulfoxide compound 2b, which is 6-7-fold less cytotoxic than its sulfide 2a, appears to be a potential bioreductive anticancer prodrug on the basis of its bioreductive metabolism findings.

Original languageEnglish (US)
Pages (from-to)118-128
Number of pages11
JournalMolecular Pharmaceutics
Volume2
Issue number2
DOIs
StatePublished - Mar 2005

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Pharmaceutical Science
  • Drug Discovery

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