Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
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Myeloperoxidase Inhibitory and Radical Scavenging Activities of Flavones from Pterogyne nitens
Daniara Cristina FernandesLuis Octávio RegasiniJosé Carlos Rebuglio VellosaPatrícia Mendonça PaulettiIan Castro-gamboaVanderlan Silva BolzaniOlga Maria Mascarenhas OliveiraDulce Helena Siqueira Silva
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2008 Volume 56 Issue 5 Pages 723-726

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Abstract

Two new flavone glucosides, nitensosides A and B (1, 2), together with four known compounds, sorbifolin (3), sorbifolin 6-O-β-glucopyranoside (4), pedalitin (5), and pedalitin 6-O-β-glucopyranoside (6) were isolated from Pterogyne nitens. Their structures were elucidated from 1D and 2D NMR analysis, as well as by high resolution mass spectrometry. All the isolated flavones were evaluated for their myeloperoxidase (MPO) inhibitory activity. The most active compound, pedalitin, exhibited IC50 value of 3.75 nM on MPO. Additionally, the radical-scavenging capacity of flavones 1—6 was evaluated towards ABTS and DPPH radicals and compared to standard compounds quercetin and Trolox®.

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© 2008 The Pharmaceutical Society of Japan
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