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Xanthone

About: Xanthone is a research topic. Over the lifetime, 1639 publications have been published within this topic receiving 25870 citations. The topic is also known as: 9-oxo-xanthene & Diphenyline ketone oxide.


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Journal ArticleDOI
TL;DR: A new xanthone: mangostanaxanthone VIIII [1,3,5,6,7-pentahydroxy-2-(3methylbut-2-enyl)-8-(3hydroxy-3-methyl-but-1-ENyl) xanthones] (5) and four known xanthains: mangoes I (1) and II (2), γ-mangostin (3), and mangostansaxanthones VII (4) were separated and characterized from the acetone fraction of Garcinia mang
Abstract: A new xanthone: mangostanaxanthone VIIII [1,3,5,6,7-pentahydroxy-2-(3-methylbut-2-enyl)-8-(3-hydroxy-3-methylbut-1-enyl) xanthone] (5) and four known xanthones: mangostanaxanthones I (1) and II (2), γ-mangostin (3), and mangostanaxanthone VII (4) were separated and characterized from the acetone fraction of Garcinia mangostana L., Clusiaceae (mangosteen) pericarps. Their structures were established based on various spectroscopic analyses in addition to HRMS and comparison with the literature. The α-amylase inhibitory potential of the isolated metabolites was evaluated. Compounds 1, and 5 had the highest activity with % inhibition 72.5, 86.5, and 81.8, respectively compared to acarbose (97.1%, reference α-amylase inhibitor). The molecular docking study of the tested metabolites was estimated to shade up the rational explanation of the α-amylase inhibitory activity results. Moreover, the pharmacokinetic parameters were assessed using Swiss ADME. It is noteworthy that 1, 2, and 5 had similar binding poses as the X-ray crystal structure of acarbose, whereas the other metabolites possessed different binding mode that decreased their inhibitory capacity. Thus, these data reinforced the health benefit of mangosteen as an alternative medicine to help lowering the postprandial glucose absorption. Therefore, it could have a good potential for the treatment of diabetes.

25 citations

Journal ArticleDOI
TL;DR: A new xanthone derivative, artoindonesianin C, was isolated from Artocarpus teysmanii, together with two known prenylated flavonoids, cycloartobiloxanthone and artonin J.
Abstract: A new xanthone derivative, artoindonesianin C (1), was isolated from Artocarpus teysmanii, together with two known prenylated flavonoids, cycloartobiloxanthone and artonin J. The structure of artoindonesianin C (1) was determined on the basis of MS and NMR evidence and by comparison with known related compounds.

25 citations

Journal ArticleDOI
TL;DR: In this article, the endolichenic fungus Apiospora montagnei isolated from the lichen Cladonia sp. was cultured on solid rice medium, yielding the new diterpenoid libertellenone L (1), the new pyridine alkaloid, 23-O-acetyl-N-hydroxyapiosporamide (2) and the new xanthone derivative 8hydroxy-3-hydroxymethyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ether (3

25 citations

Journal ArticleDOI
TL;DR: From the root bark of Calophyllum inophyllus L. (Guttiferae), a new xanthone named caloxanthone C (1) and 4-hydroxyxanthone (2) were isolated.
Abstract: From the root bark of Calophyllum inophyllum L. (Guttiferae), a new xanthone named caloxanthone C (1) and 4-hydroxyxanthone (2), and from the heartwood of root, a new xanthone 1-hydroxy-2-methoxyxanthone (3) in addition to three known xanthones [1,2-dimethoxy-(4), 2-hydroxy- 1-methoxy-(5)], and 6-deoxyjacareubin (6) were isolated. The structures were characterized by means of a spectroscopic analysis

25 citations

Journal ArticleDOI
TL;DR: Two new prenylated anthraquinones were isolated from the seeds of Vismia laurentii together with four known compounds; xanthone V(1) (3), physcion (4), 3-geranyloxyemodin anthrone (5) and friedelin (6).
Abstract: Two new prenylated anthraquinones, laurenquinone A (1) and B (2) were isolated from the seeds of Vismia laurentii together with four known compounds; xanthone V 1 (3), physcion (4), 3-geranyloxyemodin anthrone (5) and friedelin (6). The structures of the new metabolites were determined with the help of spectroscopic data including extensive 2D-NMR spectroscopy. The known compounds were identified by comparison of their physical and spectroscopic data with those reported in the literature. Compounds 1, 4 and 5 exhibited moderate algicidal activity against Chlorella fusca and 3 showed moderate activity against the gram-positive bacterium Bacillus megaterium.

25 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202347
202296
202146
202054
201949
201872