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A Novel Depsidone and Some New Xanthones from Garcinia species

TLDR
In this article, a depsidone named garcinisidone-A (1), six new xanthones named assiguxanthone-a (3), -B (9), -C (15), and -D (16), as well as some known xanthone, benzophenone, chromone, and biflavanone derivatives, and their structures were elucidated by spectroscopic methods.
Abstract
Constituents of three EtOH extracts of the stem bark of Garcinia assigu LANTB., Garcinia dulcis (ROXB.) KURZ., and Garcinia latissima MIQ., belonging to the Guttiferae, collected in Central Province of Papua New Guinea, were studied. A novel depsidone named garcinisidone-A (1), six new xanthones named assiguxanthone-A (3) and -B (9) and dulxanthone-A (4), -B (6), -C (7), and - D (11), and four new pyranoxanthones named latisxanthone-A (13), -B (14), -C (15), and -D (16) were isolated, as well as some known xanthone, benzophenone, chromone, and biflavanone derivatives, and their structures were elucidated by spectroscopic methods. Among these components, garcinisidone-A (1) is the first example of a depsidone derivative having a five-carbon unit (prenyl) as a substituent to be found in nature. Latisxanthone-B (14) was found to contain a hydroperoxy moiety in the molecule. This is the second example of a xanthone hydroperoxide to be found in nature.

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Xanthones and benzophenones from Garcinia griffithii and Garcinia mangostana

TL;DR: The acetone extract of the heartwood of Garcinia mangostana contained one new diprenylated xanthone (mangoxanthone) and a new benzophenone (3',6-dihydroxy-2,4,4'-trimethoxybenzophenone); their structures were established on the basis of spectroscopic studies and chemical correlation.
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Chemical studies on antioxidant mechanism of garcinol: analysis of radical reaction products of garcinol with peroxyl radicals and their antitumor activities

TL;DR: In this article, the double bond of the isopentenyl group is identified as a principal site of the antioxidant reaction of garcinol with peroxyl radicals generated by thermolysis of azo initiator azo-bis-isobutyrylnitrile.
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Characterization of tyrosinase inhibitors in the twigs of Cudrania tricuspidata and their structure-activity relationship study.

TL;DR: The twigs of Cudrania tricuspidata were found to show strong tyrosinase inhibitory activity, and further detailed component analysis resulted in the isolation of a new flavanol glucoside, (2S,3S)-2,3-trans-dihydromorin-7-O-β-d-glucoside (1), plus twenty-seven known compounds.
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Phloroglucinols, depsidones and xanthones from the twigs of Garcinia parvifolia

TL;DR: In this article, seven phloroglucinols, named parvifoliols A−G (1, 7), two depsidones, named Parvifolidones A, B (8, 9), and three xanthones were isolated from the twigs of Garcinia parviferolia along with seven known compounds: garcidepsidone B, mangostinone, rubraxanthone, dulxanthone D, 1,3,5,6-tetrahydroxyxanthones, norathyriol
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Prenylated benzoylphloroglucinols and xanthones from the leaves of Garcinia oblongifolia with antienteroviral activity.

TL;DR: An acetone extract of the leaves of Garcinia oblongifolia showed antiviral activity against enterovirus 71 (EV71) using a cytopathic effect inhibition assay and bioassay-guided fractionation yielded 12 new prenylated benzoylphloroglucinols, ob longifolins J-U (1-12), and five known compounds.
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