Evaluation of Perylenediimide Derivatives for Potential Therapeutic Benefits on Cancer Chemotherapy

dc.authoridISGOR, Belgin S/0000-0001-5716-3159
dc.authoridIsgor, Yasemin G./0000-0002-6021-257X
dc.authorscopusid55347181500
dc.authorscopusid57190741107
dc.authorscopusid7801688219
dc.authorscopusid15770540700
dc.authorwosidIsgor, Yasemin G./AAE-4859-2021
dc.authorwosidISGOR, Belgin S/B-7829-2013
dc.authorwosidIsgor, Yasemin G./B-3322-2010
dc.contributor.authorKeskin, Taner
dc.contributor.authorIsgor, Belgin S.
dc.contributor.authorIsgor, Yasemin G.
dc.contributor.authorYukruk, Funda
dc.contributor.otherChemical Engineering
dc.date.accessioned2024-07-05T14:28:22Z
dc.date.available2024-07-05T14:28:22Z
dc.date.issued2012
dc.departmentAtılım Universityen_US
dc.department-temp[Keskin, Taner; Yukruk, Funda] Balikesir Univ, Fac Art & Sci, Dept Chem, TR-10145 Cagis, Balikesir, Turkey; [Isgor, Belgin S.; Isgor, Yasemin G.] Atilim Univ, Dept Chem Engn & Appl Chem, Fac Engn, TR-06836 Ankara, Turkeyen_US
dc.descriptionISGOR, Belgin S/0000-0001-5716-3159; Isgor, Yasemin G./0000-0002-6021-257Xen_US
dc.description.abstractPerylene 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.en_US
dc.description.sponsorshipAtilim University; Balikesir University [BAP2009/40, BAP 2010/18]; Scientific and Technological Research Council of Turkey [TUBITAK-110T026]; Undersecretariat of State Planning Organization [DPT-2005-K-120-170]en_US
dc.description.sponsorshipThis work was partially supported by grants from the Atilim University (BAP 2011), Balikesir University (BAP2009/40; BAP 2010/18), The Scientific and Technological Research Council of Turkey (TUBITAK-110T026), and Undersecretariat of State Planning Organization (DPT-2005-K-120-170).en_US
dc.identifier.citation4
dc.identifier.doi10.1111/cbdd.12004
dc.identifier.endpage681en_US
dc.identifier.issn1747-0277
dc.identifier.issn1747-0285
dc.identifier.issue5en_US
dc.identifier.pmid22834711
dc.identifier.scopus2-s2.0-84867230113
dc.identifier.scopusqualityQ3
dc.identifier.startpage675en_US
dc.identifier.urihttps://doi.org/10.1111/cbdd.12004
dc.identifier.urihttps://hdl.handle.net/20.500.14411/364
dc.identifier.volume80en_US
dc.identifier.wosWOS:000309595500005
dc.identifier.wosqualityQ3
dc.institutionauthorİşgör, Sultan Belgin
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectanticancer agenten_US
dc.subjectglutathione transferaseen_US
dc.subjectperylenediimideen_US
dc.subjectsmall-molecule inhibitoren_US
dc.subjecttyrosine kinaseen_US
dc.titleEvaluation of Perylenediimide Derivatives for Potential Therapeutic Benefits on Cancer Chemotherapyen_US
dc.typeArticleen_US
dspace.entity.typePublication
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