{"title":"Nano Fe2O3/Ag/CeO2 catalyzed solvent free synthesis of 1,8 – di oxo octa hydro xanthene derivatives as potential anti-cancer agents","authors":"Mohammad Kazem Mohammadi , Nasim Kakesh","doi":"10.1016/j.jics.2025.101600","DOIUrl":null,"url":null,"abstract":"<div><div>Biologically active 1,8–dioxo-octa-hydro-xanthene derivatives were synthesized using Fe<sub>2</sub>O<sub>3</sub>/Ag/CeO<sub>2</sub> nanoparticles as a catalyst under solvent-free conditions. synthesized xanthene derivatives have Excellent yields of products and simple work-up are attractive features of this green protocol. The findings indicate that the catalyst can be used for a minimum of five cycles with only a slight decline in catalytic activity. Furthermore, the catalyst's reusability was also examined in the case of benzaldehyde at 90 °C under solvent-free conditions. Fe<sub>2</sub>O<sub>3</sub>/Ag/CeO<sub>2</sub> nanoparticles were thoroughly analyzed using XRD, FESEM, and UV techniques. Various substituted xanthenes were prepared and tested for activity against HeLa, SKOV-3, LS-180, MCF7, and Raji cell lines and cultures. The results of the cytotoxic study indicated that the compounds exhibited weak to moderate activity. The reactivity order of halogen substitution appeared to be F > Cl > Br. 3a and 3b exhibited moderate activity against cell lines. The exist of an electron-withdrawing group to the opposite aromatic ring of dihydroxyxanthene derivatives increased the anticancer activity, while the electron-donating group had the opposite effect.</div><div>Furthermore, compound 3f with fluorine substitution demonstrated higher activity, highlighting the significance of this site for the cytotoxic activity of these compounds.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101600"},"PeriodicalIF":3.2000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Indian Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0019452225000354","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Biologically active 1,8–dioxo-octa-hydro-xanthene derivatives were synthesized using Fe2O3/Ag/CeO2 nanoparticles as a catalyst under solvent-free conditions. synthesized xanthene derivatives have Excellent yields of products and simple work-up are attractive features of this green protocol. The findings indicate that the catalyst can be used for a minimum of five cycles with only a slight decline in catalytic activity. Furthermore, the catalyst's reusability was also examined in the case of benzaldehyde at 90 °C under solvent-free conditions. Fe2O3/Ag/CeO2 nanoparticles were thoroughly analyzed using XRD, FESEM, and UV techniques. Various substituted xanthenes were prepared and tested for activity against HeLa, SKOV-3, LS-180, MCF7, and Raji cell lines and cultures. The results of the cytotoxic study indicated that the compounds exhibited weak to moderate activity. The reactivity order of halogen substitution appeared to be F > Cl > Br. 3a and 3b exhibited moderate activity against cell lines. The exist of an electron-withdrawing group to the opposite aromatic ring of dihydroxyxanthene derivatives increased the anticancer activity, while the electron-donating group had the opposite effect.
Furthermore, compound 3f with fluorine substitution demonstrated higher activity, highlighting the significance of this site for the cytotoxic activity of these compounds.
期刊介绍:
The Journal of the Indian Chemical Society publishes original, fundamental, theorical, experimental research work of highest quality in all areas of chemistry, biochemistry, medicinal chemistry, electrochemistry, agrochemistry, chemical engineering and technology, food chemistry, environmental chemistry, etc.