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Pregled bibliografske jedinice broj: 1072712

Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study


Lončarić, Melita; Strelec, Ivica; Pavić, Valentina; Šubarić, Domagoj; Rastija, Vesna; Molnar, Maja
Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study // Pharmaceuticals, 13 (2020), 7; 1-21 doi:10.3390/ph13070154 (međunarodna recenzija, članak, znanstveni)


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Naslov
Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study

Autori
Lončarić, Melita ; Strelec, Ivica ; Pavić, Valentina ; Šubarić, Domagoj ; Rastija, Vesna ; Molnar, Maja

Izvornik
Pharmaceuticals (1424-8247) 13 (2020), 7; 1-21

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
lipoxygenase ; coumarins ; lipid peroxidation ; antioxidant activity ; QSAR ; molecular docking

Sažetak
Lipoxygenases (LOXs) are a family of enzymes found in plants, mammals, and microorganisms. In animals and plants, the enzyme has the capability for the peroxidation of unsaturated fatty acids. Although LOXs participate in the plant defense system, the enzyme’s metabolites can have numerous negative effects on human health. Therefore, many types of research are searching for compounds that can inhibit LOXs. The best quantitative structure–activity relationship (QSAR) model was obtained using a Genetic Algorithm (GA). Molecular docking was performed with iGEMDOCK. The inhibition of lipoxygenase was in the range of 7.1 to 96.6%, and the inhibition of lipid peroxidation was 7.0–91.0%. Among the synthesized compounds, the strongest inhibitor of soybean LOX-3 (96.6%) was found to be 3-benzoyl-7-(benzyloxy)-2Hchromen- 2-one. A lipid peroxidation inhibition of 91.0% was achieved with ethyl 7-methoxy-2-oxo- 2H-chromene-3-carboxylate. The docking scores for the soybean LOX-3 and human 5-LOX also indicated that this compound has the best affinity for these LOX enzymes. The best multiple linear QSAR model contains the atom-centered fragment descriptors C-06, RDF035p, and HATS8p. QSAR and molecular docking studies elucidated the structural features important for the enhanced inhibitory activity of the most active compounds, such as the presence of the benzoyl ring at the 3- position of coumarin’s core. Compounds with benzoyl substituents are promising candidates as potent lipoxygenase inhibitors.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Prehrambena tehnologija



POVEZANOST RADA


Projekt / tema
HRZZ-UIP-2017-05-6593 - Zelene tehnologije u sintezi heterocikličkih spojeva (Maja Molnar) - HRZZ-UIP-2017-05-6593 - Zelene tehnologije u sintezi heterocikličkih spojeva (Maja Molnar)

Ustanove
Fakultet agrobiotehničkih znanosti Osijek,
Prehrambeno-tehnološki fakultet, Osijek,
Sveučilište u Osijeku - Odjel za biologiju

Citiraj ovu publikaciju

Lončarić, Melita; Strelec, Ivica; Pavić, Valentina; Šubarić, Domagoj; Rastija, Vesna; Molnar, Maja
Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study // Pharmaceuticals, 13 (2020), 7; 1-21 doi:10.3390/ph13070154 (međunarodna recenzija, članak, znanstveni)
Lončarić, M., Strelec, I., Pavić, V., Šubarić, D., Rastija, V. & Molnar, M. (2020) Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study. Pharmaceuticals, 13 (7), 1-21 doi:10.3390/ph13070154.
@article{article, year = {2020}, pages = {1-21}, DOI = {10.3390/ph13070154}, keywords = {lipoxygenase, coumarins, lipid peroxidation, antioxidant activity, QSAR, molecular docking}, journal = {Pharmaceuticals}, doi = {10.3390/ph13070154}, volume = {13}, number = {7}, issn = {1424-8247}, title = {Lipoxygenase Inhibition Activity of Coumarin Derivatives—QSAR and Molecular Docking Study}, keyword = {lipoxygenase, coumarins, lipid peroxidation, antioxidant activity, QSAR, molecular docking} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
    • Emerging Sources Citation Index (ESCI)
  • Scopus


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