Literature DB >> 17603202

A new chromone, 11-hydroxy-sec-O-glucosylhamaudol from Ostericum koreanum.

Yeo Jin Park1, Hyoung Ja Kim, Sook Ja Lee, Ho-Young Choi, Changbae Jin, Yong Sup Lee.   

Abstract

From the ethyl acetate fraction of the roots of Ostericum koreanum, a new chromone, 11-hydroxy-sec-O-glucosylhamaudol (1) along with the known compounds: four chromones, three coumarins, six phenolic compounds, and three quinic acids were isolated. These compounds were assessed for antioxidant activities in the DPPH radical and superoxide anion radical scavenging assay systems. Among isolates, 4-(2-hydroxy-vinyl)-benzene-1,2-diol (12) showed the most potent DPPH radical scavenging activity (IC(50)=4.80+/-0.62 mug/ml) and superoxide anion radical scavenging activity (IC(50)=11.05+/-0.83 microg/ml) in the xanthine/xanthine oxidase system. The antioxidant activities of 12 were comparable to those of quercetin and luteolin.

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Year:  2007        PMID: 17603202     DOI: 10.1248/cpb.55.1065

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  5 in total

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2.  Comparative analysis of the constituents in Saposhnikoviae Radix and Glehniae Radix cum Rhizoma by monitoring inhibitory activity of nitric oxide production.

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4.  Vasorelaxant effect of osterici radix ethanol extract on rat aortic rings.

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5.  An Efficient Ionic Liquid-Mediated Extraction and Enrichment of Isoimperatorin from Ostericum koreanum (Max.) Kitagawa.

Authors:  Alice Nguvoko Kiyonga; Gyu Hwan Park; Hyun Su Kim; Young-Ger Suh; Tae Kon Kim; Kiwon Jung
Journal:  Molecules       Date:  2021-10-29       Impact factor: 4.411

  5 in total

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