Design, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents

dc.contributor.authorCapan, Irfan
dc.contributor.authorHawash, Mohammed
dc.contributor.authorJaradat, Nidal
dc.contributor.authorSert, Yusuf
dc.contributor.authorServi, Refik
dc.contributor.authorKoca, Irfan
dc.date.accessioned2026-08-12T17:38:15Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractBackgroundThe carbazole skeleton is an important structural motif occurring naturally or synthesized chemically and has antihistaminic, antioxidant, antitumor, antimicrobial, and anti-inflammatory activities.ObjectivesThis study aimed to design and synthesize a novel series of carbazole derivatives and evaluate their antiproliferative and antioxidant activities.MethodsThe synthesized compounds were characterized utilizing HRMS, H-1-, and C-13(APT)-NMR, and assessed for their anticancer, antifibrotic, and antioxidant effects utilizing reference biomedical procedures. In addition, the AutoDock Vina application was used to perform in-silico docking computations.ResultsA series of carbazole derivatives were synthesized and characterized in the current study. Compounds 10 and 11 were found to have a stronger antiproliferative effect than compounds 2-5 against HepG2, HeLa, and MCF7 cancer cell lines with IC50 values of 7.68, 10.09, and 6.44 mu M, respectively. Moreover, compound 9 showed potent antiproliferative activity against HeLa cancer cell lines with an IC50 value of 7.59 mu M. However, except for compound 5, all of the synthesized compounds showed moderate antiproliferative activities against CaCo-2 with IC50 values in the range of 43.7-187.23 mu M. All of these values were compared with the positive control anticancer drug 5-Fluorouracil (5-FU). In addition, compound 9 showed the most potent anti-fibrotic compound, and the cellular viability of LX-2 was found 57.96% at 1 mu M concentration in comparison with the positive control 5-FU. Moreover, 4 and 9 compounds showed potent antioxidant activities with IC50 values of 1.05 +/- 0.77 and 5.15 +/- 1.01 mu M, respectively.ConclusionMost of the synthesized carbazole derivatives showed promising antiproliferative, antioxidant, and antifibrotic biological effects, and further in-vivo investigations are needed to approve or disapprove these results.
dc.description.sponsorshipGazi University, Projects of Scientific Investigation Unit (Gazi BAP) [65/2018-03]
dc.description.sponsorshipWe acknowledge the grant awarded by Gazi University, Projects of Scientific Investigation Unit (Gazi BAP # 65/2018-03). The authors especially thank Prof. Dr. Fatih UCUN from the Suleyman Demirel University for his helpful contribution to Gaussian calculations, as well as the authors would like to thank An-Najah National University.
dc.identifier.doi10.1186/s13065-023-00961-y
dc.identifier.issn2661-801X
dc.identifier.issue1
dc.identifier.orcid0000-0001-5640-9700
dc.identifier.pmid37328860
dc.identifier.scopus2-s2.0-85162090731
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1186/s13065-023-00961-y
dc.identifier.urihttps://hdl.handle.net/11508/58359
dc.identifier.volume17
dc.identifier.wosWOS:001009200100003
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherBmc
dc.relation.ispartofBmc Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectCarbazole
dc.subjectAnticancer
dc.subjectAntifibrotic
dc.subjectLX-2
dc.subjectAntioxidant
dc.subjectDoxorubicin
dc.subjectMolecular docking
dc.titleDesign, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents
dc.typeArticle

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