Kaurane-type diterpenoids from Chromoleana odorata, their X-ray diffraction studies and potent α-glucosidase inhibition of 16-kauren-19-oic acid

A new diterpenoid, 15-angeloyloxy-16,17-epoxy-19-kauronic acid ( 1), along with five known metabolites, 16-kauren-19-oic acid ( 2), 6′-hydroxy-2′,3′,4,4′-tetramethoxychalcone ( 3), isosakuranetin ( 4), acacetin ( 5), and kaempferide ( 6) was isolated from the organic extracts of the roots of Chromol...

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Veröffentlicht in:Fitoterapia 2011-06, Vol.82 (4), p.642-646
Hauptverfasser: Wafo, Pascal, Kamdem, Ramsay S.T., Ali, Zulfiqar, Anjum, Shazia, Begum, Afshan, Oluyemisi, Ogbole O., Khan, Shamsun N., Ngadjui, Bonaventure T., Etoa, Xavier F., Choudhary, Muhammed Iqbal
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Sprache:eng
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Zusammenfassung:A new diterpenoid, 15-angeloyloxy-16,17-epoxy-19-kauronic acid ( 1), along with five known metabolites, 16-kauren-19-oic acid ( 2), 6′-hydroxy-2′,3′,4,4′-tetramethoxychalcone ( 3), isosakuranetin ( 4), acacetin ( 5), and kaempferide ( 6) was isolated from the organic extracts of the roots of Chromoleana odorata. Their structures were determined by spectroscopic evidences. The structures of 1 and 2 were further confirmed by single-crystal X-ray diffraction studies. Compound 2 exhibited significant α-glucosidase inhibitory and antibacterial activities against Escherichia coli and Bacillus subtilis. A new diterpenoid, 15-angeloyloxy-16,17-epoxy-19-kauronic acid, along with five known metabolite, 16-kauren-19-oic acid, was isolated from the organic extracts of the roots of Chromoleana odorata and confirmed by single-crystal X-ray diffraction studies. 16-Kauren-19-oic acid exhibited significant α-glucosidase inhibitory activity. [Display omitted]
ISSN:0367-326X
1873-6971
DOI:10.1016/j.fitote.2011.02.003