| Literature DB >> 25456384 |
Marina Roussaki1, Konstantinos Zelianaios2, Eleni Kavetsou2, Stylianos Hamilakis2, Dimitra Hadjipavlou-Litina3, Christos Kontogiorgis3, Thalia Liargkova3, Anastasia Detsi2.
Abstract
In the present project, a series of coumarin analogues, were synthesised and evaluated for their antioxidant and soybean lipoxygenase inhibitory activity. A variety of structural modifications on the coumarin scaffold revealed interesting structure–activity relationships concerning the different biological assays. Prenyloxy-coumarins 9 and 10 displayed the best combined inhibition of lipid peroxidation and soybean lipoxygenase. Thiocoumarins 11 and 14 were identified as potent lipoxygenase inhibitors whereas hydrazone analogues 15 and 16 were efficient DPPH radical scavengers.Entities:
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Year: 2014 PMID: 25456384 DOI: 10.1016/j.bmc.2014.10.008
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641