Parladı, UfukYılmaz, ÜlküNoma, Samir Abbas AliAteş, BurhanKüçükbay, Hasan2024-11-182024-11-182022-01-011551-7004https://doi.org/10.24820/ark.5550190.p011.810https://www.arkat-usa.org/browse-arkivoc/browse-arkivoc/ark.5550190.p011.810https://hdl.handle.net/11452/47996A series of anthraquinone derivatives (1-11) was prepared using alkyl halides, quinizarin, and danthron. The structural analysis of new compounds was carried out by 1H, 13C NMR, IR, and UV-Vis spectroscopic techniques. Xanthine oxidase inhibitory activities of compounds were measured using allopurinol as a standard. Inhibition abilities were identified by measuring the uric acid formation at 294 nm at 37 degrees C. According to the IC50 values of the compounds, it was observed that all the compounds in the group had higher inhibition values than allopurinol.eninfo:eu-repo/semantics/openAccessUric-acidDerivativesQuinizarinDyesSensitizerAnthraquinone derivativeQuinizarinDanthronXanthine oxidaseInhibitionChemistryArticle00089139900000110.24820/ark.5550190.p011.810