Antioxidant agents in wartime: prospects for the development of new biologically active compounds based on 1,2,4-triazole derivatives
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| Název: | Antioxidant agents in wartime: prospects for the development of new biologically active compounds based on 1,2,4-triazole derivatives |
|---|---|
| Autoři: | K. K. Isaycheva, A. G. Kaplaushenko, Yu. G. Sameliuk, O. P. Shmatenko, A. M. Solomennyi |
| Zdroj: | Український журнал військової медицини, Vol 6, Iss 2 (2025) |
| Informace o vydavateli: | Ukrainian Military Medical Academy, 2025. |
| Rok vydání: | 2025 |
| Témata: | Medicine, heterocyclic molecules, 1,2,4-triazole, biological activity, antioxidant activity |
| Popis: | Introduction. This article presents an analysis of the antioxidant activity of 4-amino-5-(2-, 3-, 4-nitrophenyl)-1H-1,2,4-triazole-3-thiones and their synthetic analogues, 5-(4-methoxyphenyl, 3,4,5-trimethoxyphenyl)-1,2,4-triazole-3-thiones and their synthetic analogues, and 5-(quinolin-2-yl, 2-hydroxyquinolin-4-yl)-4-R1-1,2,4-triazole-3-thiones. The main conclusions drawn from these studies are as follows: The purpose: to evaluate the antioxidant activity of 1,2,4-triazole derivatives, specifically 4-amino-5-(2-, 3-, 4-nitrophenyl)-1H-1,2,4-triazole-3-thiones, 5-(4-methoxyphenyl-, 3,4,5-trimethoxyphenyl)-1,2,4-triazole-3-thiones, and 5-(quinolin-2-yl-, 2-hydroxyquinolin-4-yl)-4-R₁-1,2,4-triazole-3-thiones, in order to identify promising compounds with pronounced antioxidant activity for potential use in the correction of pathological conditions associated with oxidative stress, particularly among the military personnel of the Armed Forces of Ukraine. Materials and Methods: The study involved the synthesis and structural analysis of 1,2,4-triazole derivatives. The antioxidant activity was assessed using spectrophotometric and electrochemical methods, determining the ability of the studied compounds to neutralize free radicals and inhibit oxidative processes. The influence of chemical structure, particularly the nature of substituents at positions 4 and 5 of the triazole ring, on antioxidant properties was analyzed through a comparative study of the obtained results. Results. Derivatives of 5-R-3-thio-1,2,4-triazole show promise as potential matrices for the development of highly effective antioxidant agents. The antioxidant properties of these derivatives depend on the nature of the substituents at the 4 and 5 positions of the 1,2,4-triazole ring. The presence of a free SH group and its substituted products, such as thioacetic acids, their salts, and esters, also contribute to the antioxidant effect. Compounds with a greater number of electron-donating groups exhibit the highest antioxidant activity, highlighting the importance of these groups in providing effective protection against oxidative processes. Conclusions. The results of the conducted study confirm the potential of 1,2,4-triazole derivatives as compounds with antioxidant activity and provide an important scientific basis for further structural optimization to enhance their effectiveness. The obtained data contribute to the development of novel highly active antioxidant agents for the correction of pathological conditions associated with oxidative stress, particularly among the military personnel of the Armed Forces of Ukraine. |
| Druh dokumentu: | Article |
| ISSN: | 2708-6623 2708-6615 |
| DOI: | 10.46847/ujmm.2025.2(6)-125 |
| Přístupová URL adresa: | https://doaj.org/article/1bd9589e6071463eb535e1262e09de52 |
| Rights: | CC BY |
| Přístupové číslo: | edsair.doi.dedup.....b6b5601da8df190d9c1422665a13e65c |
| Databáze: | OpenAIRE |
| FullText | Text: Availability: 0 CustomLinks: – Url: https://explore.openaire.eu/search/publication?articleId=doi_dedup___%3A%3Ab6b5601da8df190d9c1422665a13e65c Name: EDS - OpenAIRE (s4221598) Category: fullText Text: View record at OpenAIRE – Url: https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=EBSCO&SrcAuth=EBSCO&DestApp=WOS&ServiceName=TransferToWoS&DestLinkType=GeneralSearchSummary&Func=Links&author=Isaycheva%20KK Name: ISI Category: fullText Text: Nájsť tento článok vo Web of Science Icon: https://imagesrvr.epnet.com/ls/20docs.gif MouseOverText: Nájsť tento článok vo Web of Science |
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| Header | DbId: edsair DbLabel: OpenAIRE An: edsair.doi.dedup.....b6b5601da8df190d9c1422665a13e65c RelevancyScore: 1033 AccessLevel: 3 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 1032.51147460938 |
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| Items | – Name: Title Label: Title Group: Ti Data: Antioxidant agents in wartime: prospects for the development of new biologically active compounds based on 1,2,4-triazole derivatives – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22K%2E+K%2E+Isaycheva%22">K. K. Isaycheva</searchLink><br /><searchLink fieldCode="AR" term="%22A%2E+G%2E+Kaplaushenko%22">A. G. Kaplaushenko</searchLink><br /><searchLink fieldCode="AR" term="%22Yu%2E+G%2E+Sameliuk%22">Yu. G. Sameliuk</searchLink><br /><searchLink fieldCode="AR" term="%22O%2E+P%2E+Shmatenko%22">O. P. Shmatenko</searchLink><br /><searchLink fieldCode="AR" term="%22A%2E+M%2E+Solomennyi%22">A. M. Solomennyi</searchLink> – Name: TitleSource Label: Source Group: Src Data: Український журнал військової медицини, Vol 6, Iss 2 (2025) – Name: Publisher Label: Publisher Information Group: PubInfo Data: Ukrainian Military Medical Academy, 2025. – Name: DatePubCY Label: Publication Year Group: Date Data: 2025 – Name: Subject Label: Subject Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Medicine%22">Medicine</searchLink><br /><searchLink fieldCode="DE" term="%22heterocyclic+molecules%2C+1%2C2%2C4-triazole%2C+biological+activity%2C+antioxidant+activity%22">heterocyclic molecules, 1,2,4-triazole, biological activity, antioxidant activity</searchLink> – Name: Abstract Label: Description Group: Ab Data: Introduction. This article presents an analysis of the antioxidant activity of 4-amino-5-(2-, 3-, 4-nitrophenyl)-1H-1,2,4-triazole-3-thiones and their synthetic analogues, 5-(4-methoxyphenyl, 3,4,5-trimethoxyphenyl)-1,2,4-triazole-3-thiones and their synthetic analogues, and 5-(quinolin-2-yl, 2-hydroxyquinolin-4-yl)-4-R1-1,2,4-triazole-3-thiones. The main conclusions drawn from these studies are as follows: The purpose: to evaluate the antioxidant activity of 1,2,4-triazole derivatives, specifically 4-amino-5-(2-, 3-, 4-nitrophenyl)-1H-1,2,4-triazole-3-thiones, 5-(4-methoxyphenyl-, 3,4,5-trimethoxyphenyl)-1,2,4-triazole-3-thiones, and 5-(quinolin-2-yl-, 2-hydroxyquinolin-4-yl)-4-R₁-1,2,4-triazole-3-thiones, in order to identify promising compounds with pronounced antioxidant activity for potential use in the correction of pathological conditions associated with oxidative stress, particularly among the military personnel of the Armed Forces of Ukraine. Materials and Methods: The study involved the synthesis and structural analysis of 1,2,4-triazole derivatives. The antioxidant activity was assessed using spectrophotometric and electrochemical methods, determining the ability of the studied compounds to neutralize free radicals and inhibit oxidative processes. The influence of chemical structure, particularly the nature of substituents at positions 4 and 5 of the triazole ring, on antioxidant properties was analyzed through a comparative study of the obtained results. Results. Derivatives of 5-R-3-thio-1,2,4-triazole show promise as potential matrices for the development of highly effective antioxidant agents. The antioxidant properties of these derivatives depend on the nature of the substituents at the 4 and 5 positions of the 1,2,4-triazole ring. The presence of a free SH group and its substituted products, such as thioacetic acids, their salts, and esters, also contribute to the antioxidant effect. Compounds with a greater number of electron-donating groups exhibit the highest antioxidant activity, highlighting the importance of these groups in providing effective protection against oxidative processes. Conclusions. The results of the conducted study confirm the potential of 1,2,4-triazole derivatives as compounds with antioxidant activity and provide an important scientific basis for further structural optimization to enhance their effectiveness. The obtained data contribute to the development of novel highly active antioxidant agents for the correction of pathological conditions associated with oxidative stress, particularly among the military personnel of the Armed Forces of Ukraine. – Name: TypeDocument Label: Document Type Group: TypDoc Data: Article – Name: ISSN Label: ISSN Group: ISSN Data: 2708-6623<br />2708-6615 – Name: DOI Label: DOI Group: ID Data: 10.46847/ujmm.2025.2(6)-125 – Name: URL Label: Access URL Group: URL Data: <link linkTarget="URL" linkTerm="https://doaj.org/article/1bd9589e6071463eb535e1262e09de52" linkWindow="_blank">https://doaj.org/article/1bd9589e6071463eb535e1262e09de52</link> – Name: Copyright Label: Rights Group: Cpyrght Data: CC BY – Name: AN Label: Accession Number Group: ID Data: edsair.doi.dedup.....b6b5601da8df190d9c1422665a13e65c |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.46847/ujmm.2025.2(6)-125 Languages: – Text: Undetermined PhysicalDescription: Pagination: PageCount: 9 StartPage: 125 Subjects: – SubjectFull: Medicine Type: general – SubjectFull: heterocyclic molecules, 1,2,4-triazole, biological activity, antioxidant activity Type: general Titles: – TitleFull: Antioxidant agents in wartime: prospects for the development of new biologically active compounds based on 1,2,4-triazole derivatives Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: K. K. Isaycheva – PersonEntity: Name: NameFull: A. G. Kaplaushenko – PersonEntity: Name: NameFull: Yu. G. Sameliuk – PersonEntity: Name: NameFull: O. P. Shmatenko – PersonEntity: Name: NameFull: A. M. Solomennyi IsPartOfRelationships: – BibEntity: Dates: – D: 30 M: 06 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 27086623 – Type: issn-print Value: 27086615 – Type: issn-locals Value: edsair – Type: issn-locals Value: edsairFT Numbering: – Type: volume Value: 6 Titles: – TitleFull: Ukrainian Journal of Military Medicine Type: main |
| ResultId | 1 |
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