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2000
Volume 32, Issue 34
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

Background

Calix[n]arenes have attracted great attention due to their biocompatibility and superior stability. When the necessary functional groups are attached to these compounds, they may have the potential to target tumor tissues. Benzimidazoles are among the anticancer drugs discovered in recent years.

Aim

The aim of this study was to design and synthesise a series of calix[4]arenes-benzimidazoles. For comparison purposes, a benzimidazole derivative was synthesized by attaching it to the diester. The anticancer effects of these compounds were investigated by performing cell proliferation, apoptosis, and cell imaging studies on cancer cell lines.

Methods

Some of the obtained compounds were synthesized by employing the methods available in literature studies, and the rest were synthesized by modifying previous methods. As a result, a total of 3 new fluorescent calix[4]arene-benzimidazole derivatives were synthesized. MTT was used for cell proliferation, and Annexin V was used for apoptosis studies. For confocal imaging studies, cells were treated with DAPI and MitoTracker dyes.

Results

Four designed calix[4]arene-benzimidazoles were successfully synthesized and structurally confirmed by 1H-NMR, 13C-NMR, and IR spectroscopy. The anticancer study on four synthesized compounds was performed. Bio-imaging studies were performed using confocal microscopy for the three successfully synthesized fluorescent compounds.

Conclusion

CB5-a and CB5-c were found to be the most effective against MCF-7 cells and CB5-b against HT-29 cells in the MTT test. Apoptosis analyses also proved that these compounds inhibited the proliferation of cancer cells. As a comparison compound, the synthesized CB5-R proved to be less cytotoxic than the fluorescent compounds by the MTT method, and we found the cationic compound to bind to the calix[4]arene more effectively than the molecule’s binding to the diester.

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References

  1. HuangF. AnslynE.V. Introduction: Supramolecular chemistry.Chem. Rev.2015115156999700010.1021/acs.chemrev.5b0035226263840
    [Google Scholar]
  2. WilliamsG.T. HaynesC.J.E. FaresM. CaltagironeC. HiscockJ.R. GaleP.A. Advances in applied supramolecular technologies.Chem. Soc. Rev.20215042737276310.1039/D0CS00948B33438685
    [Google Scholar]
  3. IsikA. OguzM. KocakA. YilmazM. Calixarenes: Recent progress in supramolecular chemistry for application in cancer therapy.J. Incl. Phenom. Macrocycl. Chem.20221025-643944910.1007/s10847‑022‑01134‑5
    [Google Scholar]
  4. ShinkaiS. Calixarenes - The third generation of supramolecules.Tetrahedron199349408933896810.1016/S0040‑4020(01)91215‑3
    [Google Scholar]
  5. FanX. GuoX. Development of calixarene-based drug nanocarriers.J. Mol. Liq.202132511524610.1016/j.molliq.2020.115246
    [Google Scholar]
  6. BaldiniL. CasnatiA. SansoneF. UngaroR. Calixarene-based multivalent ligands.Chem. Soc. Rev.200736225426610.1039/B603082N17264928
    [Google Scholar]
  7. RodikR. CherenokS. KalchenkoO. YesypenkoO. LipkowskiJ. KalchenkoV. Functional calixarenes for material and life science.Curr. Org. Chem.201822222200222210.2174/1385272822666181015141327
    [Google Scholar]
  8. Abd KarimN.F.N. SupianF.L. MusaM. AyopS.K. AzmiM.S.M. YazidM.D. YiW.Y. Calixarene derivatives: A mini-review on their synthesis and demands in nanosensors and biomedical fields.Mini Rev. Med. Chem.202323673474510.2174/138955752266622092812072736173047
    [Google Scholar]
  9. Berberan-SantosM. MarcosP.M. Calixarene Complexes: Synthesis, Properties and Applications.MDPI-Multidisciplinary Digital Publishing Institute2021
    [Google Scholar]
  10. KarakurtS. KelliciT.F. MavromoustakosT. TzakosA.G. YilmazM. Calixarenes in lipase biocatalysis and cancer therapy.Curr. Org. Chem.201620101043105710.2174/1385272820666151211192249
    [Google Scholar]
  11. OguzA. OguzM. KursunluA.N. YilmazM. A fully water-soluble Calix[4]arene probe for fluorometric and colorimetric detection of toxic hydrosulfide and cyanide ions: Practicability in living cells and food samples.Food Chem.202340113413210.1016/j.foodchem.2022.13413236115237
    [Google Scholar]
  12. OguzM. AlizadaM. GulA. KursunluA.N. YilmazM. A basket-type fluorescent sensor based calix[4]azacrown ether for multi-analytes: Practicability in living cells and real sample.Microchem. J.202116710627910.1016/j.microc.2021.106279
    [Google Scholar]
  13. OguzM. DoganB. DurdagiS. BhattiA.A. KarakurtS. YilmazM. Investigation of supramolecular interaction of quercetin with N, N-dimethylamine-functionalized p-sulfonated calix[4,8]arenes using molecular modeling and their in vitro cytotoxic response towards selected cancer cells.New J. Chem.20214539184431845210.1039/D1NJ03038H
    [Google Scholar]
  14. OguzM. BhattiA.A. DoganB. KarakurtS. DurdagiS. YilmazM. Formation of the inclusion complex of water soluble fluorescent calix[4]arene and naringenin: Solubility, cytotoxic effect and molecular modeling studies.J. Biomol. Struct. Dyn.202038133801381310.1080/07391102.2019.166830131526236
    [Google Scholar]
  15. NeriP. SesslerJ.L. WangM-X. Calixarenes and beyond.Springer201610.1007/978‑3‑319‑31867‑7
    [Google Scholar]
  16. de FátimaA. FernandesS. SabinoA. Calixarenes as new platforms for drug design.Curr. Drug Discov. Technol.20096215117010.2174/15701630978848830219519339
    [Google Scholar]
  17. PanY.C. HuX.Y. GuoD.S. Biomedical applications of calixarenes: State of the art and perspectives.Angew. Chem. Int. Ed.20216062768279410.1002/anie.20191638031965674
    [Google Scholar]
  18. TauranY. ColemanA. PerretF. KimB. Cellular and in vivo biological activities of the calix[n]arenes.Curr. Org. Chem.201519232250227010.2174/1385272819666150608222114
    [Google Scholar]
  19. ShurpikD.N. PadnyaP.L. StoikovI.I. CraggP.J. Antimicrobial activity of calixarenes and related macrocycles.Molecules20202521514510.3390/molecules2521514533167339
    [Google Scholar]
  20. NimseS.B. KimT. Biological applications of functionalized calixarenes.Chem. Soc. Rev.201342136638610.1039/C2CS35233H23032718
    [Google Scholar]
  21. HussainM.A. AshrafM.U. MuhammadG. TahirM.N. BukhariS.N.A. Calixarene: A versatile material for drug design and applications.Curr. Pharm. Des.201723162377238827779081
    [Google Scholar]
  22. PaulS. JeyaprakashR.S. PaiA. VenkatachalamH. JayashreeB.S. Calixarenes and their relevance in anticancer drug development.Med. Chem.2023191093994510.2174/157340641966623070311460537403386
    [Google Scholar]
  23. Da SilvaE. LazarA.N. ColemanA.W. Biopharmaceutical applications of calixarenes.J. Drug Deliv. Sci. Technol.200414132010.1016/S1773‑2247(04)50001‑1
    [Google Scholar]
  24. DingsR.P.M. LevineJ.I. BrownS.G. Astorgues-XerriL. MacDonaldJ.R. HoyeT.R. RaymondE. MayoK.H. Polycationic calixarene PTX013, a potent cytotoxic agent against tumors and drug resistant cancer.Invest. New Drugs20133151142115010.1007/s10637‑013‑9932‑023392775
    [Google Scholar]
  25. NaseerM.M. AhmedM. HameedS. Functionalized calix[4]arenes as potential therapeutic agents.Chem. Biol. Drug Des.201789224325610.1111/cbdd.1281828205403
    [Google Scholar]
  26. OguzM. GulA. KarakurtS. YilmazM. Synthesis and evaluation of the antitumor activity of Calix[4]arene l-proline derivatives.Bioorg. Chem.20209410320710.1016/j.bioorg.2019.10320731451296
    [Google Scholar]
  27. OguzM. Synthesis and anticancer activity of new p-tertbutylcalix[4]arenes integrated with trifluoromethyl aniline groups against several cell lines.Tetrahedron202211613281610.1016/j.tet.2022.132816
    [Google Scholar]
  28. OguzM. YildirimA. DurmusI.M. KarakurtS. YilmazM. Synthesis of new calix[4]arene derivatives and evaluation of their cytotoxic activity.Med. Chem. Res.2021315259
    [Google Scholar]
  29. AnL. WangC. ZhengY.G. LiuJ. HuangT. Design, synthesis and evaluation of calix[4]arene-based carbonyl amide derivatives with antitumor activities.Eur. J. Med. Chem.202121011298410.1016/j.ejmech.2020.11298433183867
    [Google Scholar]
  30. AnL. HanL.L. ZhengY.G. PengX.N. XueY.S. GuX.K. SunJ. YanC.G. Synthesis, X-ray crystal structure and anti-tumor activity of calix[n]arene polyhydroxyamine derivatives.Eur. J. Med. Chem.2016123213010.1016/j.ejmech.2016.07.01627474920
    [Google Scholar]
  31. YoussifB.G.M. MorcossM.M. BräseS. Abdel-AzizM. Abdel-RahmanH.M. Abou El-EllaD.A. AbdelhafezE.S.M.N. Benzimidazole-based derivatives as apoptotic Antiproliferative agents: Design, synthesis, docking, and mechanistic studies.Molecules202429244610.3390/molecules2902044638257358
    [Google Scholar]
  32. AlamgirM. BlackD.S.C. KumarN. Synthesis, reactivity and biological activity of benzimidazoles. Bioactive Heterocycles III. Topics in Heterocyclic ChemistrySpringerBerlin, Heidelberg2007987118
    [Google Scholar]
  33. TanY.J. LeeY.T. YeongK.Y. PetersenS.H. KonoK. TanS.C. OonC.E. Anticancer activities of a benzimidazole compound through sirtuin inhibition in colorectal cancer.Future Med. Chem.201810172039205710.4155/fmc‑2018‑005230066578
    [Google Scholar]
  34. SalahuddinM. ShaharyarM. MazumderA. Benzimidazoles: A biologically active compounds.Arab. J. Chem.201710S157S17310.1016/j.arabjc.2012.07.017
    [Google Scholar]
  35. OzkanS.C. AksakalF. YilmazA. Synthesis of novel calix[4]arene p-benzazole derivatives and investigation of their DNA binding and cleavage activities with molecular docking and experimental studies.RSC Advances20201063386953870810.1039/D0RA07486A35517565
    [Google Scholar]
  36. BansalY. SilakariO. The therapeutic journey of benzimidazoles: A review.Bioorg. Med. Chem.201220216208623610.1016/j.bmc.2012.09.01323031649
    [Google Scholar]
  37. El-RashedyA.A. Magd El-DinA.A. YousifN.M. YousifM.N.M. Recent trends on synthesis of Benzimidazoles.Antiinfect. Agents2024222e30112322408310.2174/0122113525276208231116121402
    [Google Scholar]
  38. MavvajiM. AkkocS. Recent advances in the application of heterogeneous catalysts for the synthesis of benzimidazole derivatives.Coord. Chem. Rev.202450521571410.1016/j.ccr.2024.215714
    [Google Scholar]
  39. GoyalK. SharmaA. AryaR. SharmaR. GuptaG.K. SharmaA.K. Double edge sword behavior of Carbendazim: A potent fungicide with anticancer therapeutic properties. Anticancer. Agents Med. Chem.20181813845
    [Google Scholar]
  40. DarwishS.A. El-KerdawyM.M. ElsheakhA.R. AbdelrahmanR.S. ShaldamM.A. Abdel-AzizH.A. HassanG.S. GhalyM.A. New tilomisole-based benzimidazothiazole derivatives as anti-inflammatory agents: Synthesis, in vivo, in vitro evaluation, and in silico studies.Bioorg. Chem.202212010564410.1016/j.bioorg.2022.10564435121552
    [Google Scholar]
  41. PetersenJ.S.S.M. BairdS.K. Treatment of breast and colon cancer cell lines with anti-helmintic benzimidazoles mebendazole or albendazole results in selective apoptotic cell death.J. Cancer Res. Clin. Oncol.2021147102945295310.1007/s00432‑021‑03698‑034148157
    [Google Scholar]
  42. OguzA. SaglikB.N. OguzM. OzturkB. YilmazM. Novel mitochondrial and DNA damaging fluorescent Calix[4]arenes bearing isatin groups as aromatase inhibitors: Design, synthesis and anticancer activity.Bioorg. Med. Chem.20249811758610.1016/j.bmc.2023.11758638171252
    [Google Scholar]
  43. FangJ.A. ZhaoJ.L. LiaoX. ZengX. ChenK. WeiX.Y. SuS.B. LuoQ.Y. RedshawC. JinZ. Molecular tweezers-like calix[4]arene based alkaline earth metal cation (Ca2+, Sr2+, and Ba2+) chemosensor and its imaging in living cells and zebrafish.Inorg. Chem.20195821147201472710.1021/acs.inorgchem.9b0236431613605
    [Google Scholar]
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