Research Article
Evaluation of Perylenediimide Derivatives for Potential Therapeutic Benefits on Cancer Chemotherapy
Article first published online: 31 AUG 2012
DOI: 10.1111/cbdd.12004
© 2012 John Wiley & Sons A/S
Additional Information
How to Cite
Keskin, T., Isgor, B. S., Isgor, Y. G. and Yukruk, F. (2012), Evaluation of Perylenediimide Derivatives for Potential Therapeutic Benefits on Cancer Chemotherapy. Chemical Biology & Drug Design, 80: 675–681. doi: 10.1111/cbdd.12004
Publication History
- Issue published online: 5 OCT 2012
- Article first published online: 31 AUG 2012
- Accepted manuscript online: 26 JUL 2012 08:45PM EST
- Received 22 January 2012, revised 12 June 2012 and accepted for publication 16 July 2012
- Abstract
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Keywords:
- anticancer agent;
- glutathione transferase;
- perylenediimide;
- small-molecule inhibitor;
- tyrosine kinase
Perylene derivatives, known to have potential therapeutic benefits on particular cancer types as photosensitizers, may also function as small-molecule inhibitors with promising therapeutic value for diverse diseases. This recently recognized biological activity was attributed to their capacity to modulate the function of various enzymes as biological targets in vitro. Although the inhibitory activity on glutathione transferase and Src tyrosine kinase is important in determining the anticancer potential of compounds for target-specific drug design and development, to date, there are no successful inhibitors of this kind. Moreover, there are only a few studies about the effects of perylene derivatives on glutathione transferase and various kinases. In this study, four novel perylene compounds, N,N′-disubstituted perylenediimides and their 1,7-dibromo derivatives, were synthesized and evaluated for their biological activities. Here, among the compounds analyzed, one of them was identified with strong glutathione transferase inhibition and two with dual activity for both glutathione transferase and c-src inhibition. These results revealed that perylene derivatives may be employed as potential chemosensitizers to prevent chemotherapy-dependent drug resistance and identified as prospective anticancer agents with dual activity on both glutathione transferase and c-src enzymes.

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