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https://open.uns.ac.rs/handle/123456789/30503
Nаziv: | Microwave assisted synthesis and biomedical potency of salicyloyloxy and 2-methoxybenzoyloxy androstane and stigmastane derivatives | Аutоri: | Penov-Gaši Katarina Đurendić Evgenija Mihály Szécsi János Gardi Čanadi Janoš Klisurić Olivera Dojčinović-Vujašković S. V Nikolić (Gaković) Andrea Savić Marina P. Ajduković Jovana Oklješa Aleksandar Kojić Vesna Sakač Marija Jovanović-Šanta Suzana |
Dаtum izdаvаnjа: | 2015 | Čаsоpis: | Steroids | Sažetak: | © 2014 Elsevier Inc. All rights reserved. A convenient microwave assisted solvent free synthesis as well as conventional synthesis of salicyloyloxy and 2-methoxybenzoyloxy androstane and stigmastane derivatives 7-19 from appropriate steroidal precursors 1-6 and methyl salicylate is reported. The microwave assisted synthesis in most cases was more successful regarding reaction time and product yields. It was more environmentally friendly too, compared to the conventional method. The antioxidant activity and cytotoxicity of the synthesized derivatives were evaluated in a series of in vitro tests, as well as their inhibition potency exerted on hydroxysteroid dehydrogenase enzymes (Δ 5 -3βHSD, 17βHSD2 and 17βHSD3). All of the tested compounds were effective in OH radical neutralization, particularly compounds 9, 11 and 14, which exhibited about 100-fold stronger activity than commercial antioxidants BHT and BHA. In DPPH radical scavenging new compounds were effective, but less than reference compounds. 2-Methoxybenzoyl ester 10 exhibited strong cytotoxicity against MDA-MB-231 cells. Most compounds inhibited growth of PC-3 cells, where salicyloyloxy stigmastane derivative 15 showed the best inhibition potency. Compounds 9, 10 and 11 were the best inhibitors of 17βHSD2 enzyme. X-ray structure analysis and molecular mechanics calculations (MMC) were performed for the best cytotoxic agents, compounds 10 and 15. A comparison of crystal and MMC structures of compounds 10 and 15 revealed that their molecules conformations are stable even after releasing of the influence of crystalline field and that the influence of crystal packing on molecular conformation is not predominant. | URI: | https://open.uns.ac.rs/handle/123456789/30503 | ISSN: | 0039-128X | DOI: | 10.1016/j.steroids.2014.12.008 |
Nаlаzi sе u kоlеkciјаmа: | PMF Publikacije/Publications |
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