Determination of Antioxidant Capacity of 2,6-Quinolinediol

MakaleAçık Erişim
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

The compounds of the quinolone group have been widely used in the alive metabolism,paint and pharmaceutical industry. Therefore, various quinoline derivatives are synthesized andsynthesis methods are developed. The synthesis of the quinoline compounds in the industrial field isformed in a separate area. 2,6-quinolinediol is derivative a quinoline. In this study, differentbioanalytical methods such as reducing capacity by Fe3+-Fe2+ transformation method, Fe3+-TPTZreducing capacity by FRAP method, Cu2+-Cu+reducing capacity by CUPRAC method, the ferric ions(Fe2+) chelating activity by using bipyridyl reagent, DPPH, ABTS, DMPD radical scavengingactivities, superoxide anion radicals (O2.-) scavenging activity have been used. Also, Trolox, αTocopherol, BHA and BHT have been used as reference antioxidants. The IC50 inhibition value of theABTS radical removal activity for this substance was calculated as 3.39 µg mL-1. Referenceantioxidants such as trolox, BHA, α-Tocopherol and BHT exhibited ABTS radical removal inhibitionsat 2.59, 4.44, 7.07 and 32.36 µg mL-1, respectively. Studies have shown that 2,6-quinolinediol is aneffective antioxidant.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/17973Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.21597/jist.553129Yayıncı resmi DOI adresi
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Atıflar
OpenAlex
4
TR Dizin
2
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTopal, Fevzi
dc.date.accessioned2026-10-22T10:39:26.641294683Z
dc.date.available2026-10-22T10:39:26.641294683Z
dc.date.issued2019
dc.description.abstractThe compounds of the quinolone group have been widely used in the alive metabolism,paint and pharmaceutical industry. Therefore, various quinoline derivatives are synthesized andsynthesis methods are developed. The synthesis of the quinoline compounds in the industrial field isformed in a separate area. 2,6-quinolinediol is derivative a quinoline. In this study, differentbioanalytical methods such as reducing capacity by Fe3+-Fe2+ transformation method, Fe3+-TPTZreducing capacity by FRAP method, Cu2+-Cu+reducing capacity by CUPRAC method, the ferric ions(Fe2+) chelating activity by using bipyridyl reagent, DPPH, ABTS, DMPD radical scavengingactivities, superoxide anion radicals (O2.-) scavenging activity have been used. Also, Trolox, αTocopherol, BHA and BHT have been used as reference antioxidants. The IC50 inhibition value of theABTS radical removal activity for this substance was calculated as 3.39 µg mL-1. Referenceantioxidants such as trolox, BHA, α-Tocopherol and BHT exhibited ABTS radical removal inhibitionsat 2.59, 4.44, 7.07 and 32.36 µg mL-1, respectively. Studies have shown that 2,6-quinolinediol is aneffective antioxidant.
dc.identifier.doi10.21597/jist.553129
dc.identifier.eissn2536-4618
dc.identifier.endpage1527
dc.identifier.issn2146-0574
dc.identifier.issue3
dc.identifier.startpage1520
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/17973
dc.identifier.volume9
dc.language.isoen
dc.relation.ispartofIğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectKimya, Uygulamalı
dc.subjectKimya, Organik
dc.subjectKimya, Tıbbi
dc.titleDetermination of Antioxidant Capacity of 2,6-Quinolinediol
dc.typeArticle
rdl.citation.openalex4
rdl.citation.trdizin2
rdl.oa.statusbronze
rdl.oa.urlhttps://dergipark.org.tr/en/download/article-file/786139
rdl.sdgSDG03
rdl.source.indexTRDIZIN