Synthesis and Biological Evaluation of Novel Paracetamol-Triazole Conjugates

dc.authorscopusid57190582389
dc.authorscopusid57223437357
dc.authorscopusid39161700400
dc.authorscopusid58027927500
dc.authorscopusid57192925338
dc.authorscopusid26638740000
dc.authorscopusid13409447800
dc.contributor.authorKulabaş, N.
dc.contributor.authorGürboǧa, M.
dc.contributor.authorÖzakpinar, Ö.B.
dc.contributor.authorLiu, J.
dc.contributor.authorJakobsson, P.-J.
dc.contributor.authorDaniş, Ö.
dc.contributor.authorKüçükgüzel, I.
dc.date.accessioned2025-03-10T21:19:08Z
dc.date.available2025-03-10T21:19:08Z
dc.date.issued2023
dc.departmentFenerbahçe Universityen_US
dc.department-tempKulabaş N., Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Marmara University, Başibüyük, Istanbul, Turkey; Gürboǧa M., Department of Biochemistry, Faculty of Pharmacy, Marmara University, Başibüyük, Istanbul, Turkey; Özakpinar Ö.B., Department of Biochemistry, Faculty of Pharmacy, Marmara University, Başibüyük, Istanbul, Turkey; Liu J., Rheumatology Division, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden; Jakobsson P.-J., Rheumatology Division, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden; Daniş Ö., Department of Chemistry, Faculty of Science, Marmara University, Istanbul, Turkey; Ogan A., Department of Chemistry, Faculty of Science, Marmara University, Istanbul, Turkey; Küçükgüzel I., Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Fenerbahçe University, Ataşehir, Istanbul, Turkeyen_US
dc.description.abstractSome new triazole containing acetamide derivatives 9-20 using paracetamol as starting material were synthesized, and their structures were verified by FTIR, NMR (1H and 13C) and mass spectral data. Compounds 9-20 were tested against five human cancer cell lines (lung cancer A549, chronic myelogenous leukemia K562, breast cancer MCF-7, prostate cancer PC-3, neuroblastoma SH-SY5Y cell lines) for in vitro cytotoxic activities. They were also evaluated their cytotoxic effect on mouse embryonic fibroblast cells (NIH/3T3) to define selectivity by MTT assay. Additionally, we evaluated the potential mPGES-1 and COX-1/2 inhibitory effect of twelve target compounds 9-20. While none of the synthesized compounds exhibited significant inhibition against both cancer cells and mPGES-1 as well as COX-1/2, it was determined that they were not cytotoxic against healthy cells, too. Finally, ADMET properties of newly synthesized compounds were estimated using in silico methods. © 2023 Society of Pharmaceutical Sciences of Ankara (FABAD). All rights reserved.en_US
dc.description.sponsorshipEuropean Commission, EC; Horizon 2020 Framework Programme, H2020; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK, (218S549); Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, TÜBİTAK; H2020 Marie Skłodowska-Curie Actions, MSCA, (812890); H2020 Marie Skłodowska-Curie Actions, MSCAen_US
dc.identifier.doi10.55262/fabadeczacilik.1336831
dc.identifier.endpage410en_US
dc.identifier.issn1300-4182
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-85196581992
dc.identifier.scopusqualityQ4
dc.identifier.startpage395en_US
dc.identifier.urihttps://doi.org/10.55262/fabadeczacilik.1336831
dc.identifier.urihttps://hdl.handle.net/20.500.14627/846
dc.identifier.volume48en_US
dc.identifier.wosqualityN/A
dc.language.isoenen_US
dc.publisherSociety of Pharmaceutical Sciences of Ankara (FABAD)en_US
dc.relation.ispartofFabad Journal of Pharmaceutical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.scopus.citedbyCount1
dc.subject1,2,4-Triazoleen_US
dc.subjectCanceren_US
dc.subjectCox-1/2en_US
dc.subjectMpges-1en_US
dc.subjectParacetamolen_US
dc.titleSynthesis and Biological Evaluation of Novel Paracetamol-Triazole Conjugatesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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