
Two new flavone glucosides, nitensosides A and B (1, 2), together with four known compounds, sorbifolin (3), sorbifolin 6-O-beta-glucopyranoside (4), pedalitin (5), and pedalitin 6-O-beta-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.
Magnetic Resonance Spectroscopy, Radical scavenging, Glucosides, Picrates, nitensoside a, pedalitin 6 o beta glucopyranoside, nitensoside b, flavone derivative, controlled study, Benzothiazoles, drug inhibition, Enzyme Inhibitors, Flavone, Peroxidase, Myeloperoxidase, nonhuman, sorbifolin 6 o beta glucopyranoside, Biphenyl Compounds, IC 50, Fabaceae, legume, Free Radical Scavengers, Flavones, Plant Leaves, myeloperoxidase, drug structure, nuclear magnetic resonance, pedalitin, sorbifolin, Pterogyne nitens, Antioxidant, Sulfonic Acids, glucoside
Magnetic Resonance Spectroscopy, Radical scavenging, Glucosides, Picrates, nitensoside a, pedalitin 6 o beta glucopyranoside, nitensoside b, flavone derivative, controlled study, Benzothiazoles, drug inhibition, Enzyme Inhibitors, Flavone, Peroxidase, Myeloperoxidase, nonhuman, sorbifolin 6 o beta glucopyranoside, Biphenyl Compounds, IC 50, Fabaceae, legume, Free Radical Scavengers, Flavones, Plant Leaves, myeloperoxidase, drug structure, nuclear magnetic resonance, pedalitin, sorbifolin, Pterogyne nitens, Antioxidant, Sulfonic Acids, glucoside
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