Synthesis, Molecular Modeling and Biological Assessment of Aryloxymethyl 1,3,4-Thiadiazole and 1,2,4-Triazole-5-Thione Derivatives as Potential Cox Inhibitors
dc.contributor.author | Shirzad, Mohammad Musa | |
dc.contributor.author | Ozadali-Sari, Keriman | |
dc.contributor.author | Unsal-Tan, Oya | |
dc.contributor.author | Husseini, Abbas Ali | |
dc.contributor.author | Palaska, Erhan | |
dc.date.accessioned | 2024-09-11T19:50:24Z | |
dc.date.available | 2024-09-11T19:50:24Z | |
dc.date.issued | 2024 | |
dc.department | İstanbul Gelişim Üniversitesi | en_US |
dc.description.abstract | Thiadiazole and triazole-5-thione derivatives are five membered heterocyclic compounds showing cyclooxygenase inhibition activities. Based on this observation a series of novel aryloxymethyl 1,3,4-thiadiazole and 1,2,4-triazole-5-thione derivatives were synthesized and their biological activities evaluated. The suggested chemical structure of synthesized compounds was confirmed using FT-IR, Mass, 1H-NMR, and 13C-NMR spectrometric methods and elemental analysis. The biological activity or potency of synthesized compounds was evaluated using a COX inhibitor screening assay kit (Cayman Chemical Company), and indomethacin and NS398 as standard compounds. Compounds 2b and 3b showed good inhibitory activity against COX-2 and COX-1 enzymes respectively. The obtained data indicate that compound 2b is more selective to COX-2 and compound 3b is more selective to COX-1 compared with other synthesized compounds. These two compounds show promising selectivity and could be a starting point for future research in this area. | en_US |
dc.description.sponsorship | Research council of Hacettepe University, Institute Health Science | en_US |
dc.description.sponsorship | This study was supported by grants from the research council of Hacettepe University, Institute Health Science. | en_US |
dc.identifier.doi | 10.1007/s11094-024-03136-8 | |
dc.identifier.endpage | 215 | en_US |
dc.identifier.issn | 0091-150X | |
dc.identifier.issn | 1573-9031 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopus | 2-s2.0-85197641439 | en_US |
dc.identifier.startpage | 209 | en_US |
dc.identifier.uri | https://doi.org/10.1007/s11094-024-03136-8 | |
dc.identifier.uri | https://hdl.handle.net/11363/7624 | |
dc.identifier.volume | 58 | en_US |
dc.identifier.wos | WOS:001252346500009 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Pharmaceutical Chemistry Journal | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.snmz | 20240903_G | en_US |
dc.subject | thiadiazole | en_US |
dc.subject | triazole | en_US |
dc.subject | cyclooxygenase | en_US |
dc.subject | inflammation | en_US |
dc.subject | docking | en_US |
dc.title | Synthesis, Molecular Modeling and Biological Assessment of Aryloxymethyl 1,3,4-Thiadiazole and 1,2,4-Triazole-5-Thione Derivatives as Potential Cox Inhibitors | en_US |
dc.type | Article | en_US |