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Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase (CROSBI ID 555240)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Katalinić, Maja ; Rusak, Gordana ; Domaćinović Barović, Jelena ; Šinko, Goran ; Jelić, Dubravko ; Antolović, Roberto ; Kovarik, Zrinka Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase // 10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts / Kovarik, Zrinka (ur.). Zagreb: Hrvatsko društvo za biokemiju i molekularnu biologiju (HDBMB), 2009. str. 99-99

Podaci o odgovornosti

Katalinić, Maja ; Rusak, Gordana ; Domaćinović Barović, Jelena ; Šinko, Goran ; Jelić, Dubravko ; Antolović, Roberto ; Kovarik, Zrinka

engleski

Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase

Selected flavonoids: galangin, kaempferol, quercetin, myricetin, fisetin, apigenin, luteolin and rutin, reversibly inhibited human butyrylcholinesterase (BChE, EC 3.1.1.8). Inhibition potency of the flavonoids we attributed to their chemical structure, i.e., the number of OH groups and their side on the phenyl ring. The most potent BChE inhibitor among the tested flavonoids was galangin, which showed 12 times higher preference for binding to BChE (Ki = 7 μ mol/L) than to the related enzyme human acetylcholinesterase (AChE, EC 3.1.1.7). Docking study showed that flavonoids bind to the BChE active site by forming multiple hydrogen bonds and π -π interactions. The UV-VIS (200-500 nm) absorption spectra of the flavonoid phosphate buffer solution (pH 7.4), with the exception of rutin, revealed time dependant changes indicating precipitation of flavonoids or in the case of myricetin, a change in the chemical structure resulting in a BChE non-inhibiting specie. Selected flavonoids showed no cytotoxic effect on HepG2 and A549 cell lines at concentrations up to 200 μ mol/L. Cytotoxicity was observed only for fisetin, apigenin and luteolin in the THP-1 cell line with IC50 of 30, 60 and 70 μ mol/L, respectively. Galangin is therefore singled out as a promising hit in the search for new BChE inhibitors.

Acetylcholinesterase; Cholinesterase; Cytotoxicity; Flavonoids; UV-VIS spectra; Reversible inhibition

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Podaci o prilogu

99-99.

2009.

objavljeno

Podaci o matičnoj publikaciji

10th International Meeting on Cholinesterases, Šibenik, Hrvatska, Programme and Abstracts

Kovarik, Zrinka

Zagreb: Hrvatsko društvo za biokemiju i molekularnu biologiju (HDBMB)

978-953-95551-3-7

Podaci o skupu

10th International Meeting on Cholinesterases

poster

20.09.2009-25.09.2009

Šibenik, Hrvatska

Povezanost rada

Kemija, Biologija