2″,4″-<i>O</i>-Diacetylquercitrin, a Novel Advanced Glycation End-Product Formation and Aldose Reductase Inhibitor from <i>Melastoma sanguineum</i>
Advanced glycation end-product
DOI:
10.1248/cpb.c12-00877
Publication Date:
2013-06-01T04:12:47Z
AUTHORS (6)
ABSTRACT
A new flavonoid, 2,″4″-O-diacetylquercitrin (1), along with six known flavonoids (2–7) were isolated from the aerial parts of Melastoma sanguineum. The structure flavonoid was established by extensive spectroscopic studies and chemical evidence. inhibitory effects compounds (1–7) on advanced glycation end-products (AGEs) formation rat lens aldose reductase (RLAR) in vitro examined. Of tested compounds, compound 1 strongest inhibitor AGEs, an IC50 11.46±0.44 µm. In RLAR assay, all exhibited greater than that a positive control, 3,3-tetramethyleneglutaric acid (IC50=28.8±1.5 µm); RLAR-inhibitory activity, 0.077±0.003
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