Xanthine oxidase inhibitors from Brandisia hancei

Citation
Ld. Kong et al., Xanthine oxidase inhibitors from Brandisia hancei, PLANTA MED, 65(8), 1999, pp. 744-746
Citations number
13
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PLANTA MEDICA
ISSN journal
00320943 → ACNP
Volume
65
Issue
8
Year of publication
1999
Pages
744 - 746
Database
ISI
SICI code
0032-0943(199912)65:8<744:XOIFBH>2.0.ZU;2-A
Abstract
Xanthine oxidase is a key enzyme associated with the incidence of hyperuric emia-related disorders. Repeated chromatography of the enzyme inhibitory pa rt of the water extract of the twigs and leaves of Brandisia hancei (Scroph ulariaceae) gave a flavone luteolin, an iridoid glycoside mussaenoside, two beta-sitosterol glycosides daucosterol and beta-sitosterol gentiobioside, and five phenylethanoids arenarioside, brandioside, acteoside, 2'-O-acetyla cteoside and isoacteoside. Luteolin and isoacteoside inhibited the xanthine oxidase (XO, EC 1.2.3.2) with the IC50 values at 7.83 and 45.48 mu M, resp ectively. Isoacteoside was found to be the first phenylethanoid that decrea sed substantially the formation of uric acid by inhibiting competitively xa nthine oxidase (K-i value: 10.08 mu M). Furthermore, the study suggested th at the caffeoylation of the 6'-hydroxyl group of the phenylethanoids was es sential for the enzyme inhibitory action.