Academic Journal

Antioxidant, Antimicrobial and Antiproliferative Activities of Synthesized 2,2,5,5-Tetramethyl-9-aryl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione Derivatives

التفاصيل البيبلوغرافية
العنوان: Antioxidant, Antimicrobial and Antiproliferative Activities of Synthesized 2,2,5,5-Tetramethyl-9-aryl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione Derivatives
المؤلفون: Zukic, Selma, Veljović, Elma, Špirtović-Halilović, Selma, Muratovic, Samija, Osmanović, Amar, Trifunović, Snežana S., Novaković, Irena T., Završnik, Davorka
المصدر: Croatica Chemica Acta
بيانات النشر: Croatian Chemical Soc, Zagreb
سنة النشر: 2018
المجموعة: CHERRY - CHEMistry RepositorY, Faculty of Chemistry, University of Belgrade / Repozitorijum Hemijskog fakulteta - Cherry (Univerzitet u Beogradu - Hemijski fakultet)
مصطلحات موضوعية: xanthene-1,8-diones, antimicrobial activity, antiproliferative activity, antioxidant potency
الوصف: Ten biologically active 2,2,5,5-tetramethy1-9-aryl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione derivatives were synthesized and their structures were confirmed by IR, H-1 and C-13 NMR spectroscopy and mass spectrometry. Synthesized compounds were scanned for their antioxidant, antimicrobial and antiproliferative activity. Antibacterial activity was tested by the diffusion and dilution method against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, while a ntifunga I activity was tested against Candida albicans and Saccharomyces cerevisiae. Antiproliferative activity was tested against HeLa (cervical carcinoma), SW620 (colorectal adenocarcinoma, metastatic), hepatocellular carcinoma (HEpG2), lung carcinoma cells (A549) and mouse embryo fibroblast cell line (3T3). The best antioxidant activity showed compound 2 with two hydroxy groups substituted on phenyl ring in positions 2' and 3'. The best antimicrobial activity of all synthesized compounds showed compound 8, while the best antiproliferative activity showed compound 6. Results signify the importance of xanthene-1,8-dione derivatives as potential antioxidant and antiproliferative agents.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 0011-1643
Relation: https://cherry.chem.bg.ac.rs/handle/123456789/2231; 000447334900001; 2-s2.0-85047193004; https://cherry.chem.bg.ac.rs/bitstream/id/9230/2229.pdf
DOI: 10.5562/cca3225
الاتاحة: https://cherry.chem.bg.ac.rs/handle/123456789/2231
https://doi.org/10.5562/cca3225
https://cherry.chem.bg.ac.rs/bitstream/id/9230/2229.pdf
Rights: openAccess ; https://creativecommons.org/licenses/by/4.0/ ; BY
رقم الانضمام: edsbas.B8FB3062
قاعدة البيانات: BASE
الوصف
تدمد:00111643
DOI:10.5562/cca3225