Four isoflavanones from the stem bark of Platycelphium voe¨nse

dc.contributor.authorGumula , Ivan
dc.contributor.authorHeydenreich, Matthias
dc.contributor.authorNdiege, Isaiah O.
dc.contributor.authorYenesew, Abiy
dc.date.accessioned2025-02-24T15:04:26Z
dc.date.available2025-02-24T15:04:26Z
dc.date.issued2012-08-20
dc.description.abstractFrom the stem bark of Platycelphium voënse (Leguminosae) four new isoflavanones were isolated and characterized as (S)-5,7-dihydroxy-2′,4′-dimethoxy-3′-(3″-methylbut-2″-enyl)-isoflavanone (trivial name platyisoflavanone A), (±)-5,7,2′-trihydroxy-4′-methoxy-3′-(3″-methylbut-2″-enyl)-isoflavanone (platyisoflavanone B), 5,7-dihydroxy-4′-methoxy-2″-(2‴-hydroxyisopropyl)-dihydrofurano-[4″,5″:3′,2′]-isoflavanone (platyisoflavanone C) and 5,7,2′,3″-tetrahydroxy-2″,2″-dimethyldihydropyrano-[5″,6″:3′,4′]-isoflavanone (platyisoflavanone D). In addition, the known isoflavanones, sophoraisoflavanone A and glyasperin F; the isoflavone, formononetin; two flavones, kumatakenin and isokaempferide; as well as two triterpenes, betulin and β-amyrin were identified. The structures were elucidated on the basis of spectroscopic evidence. Platyisoflavanone A showed antibacterial activity against Mycobacterium tuberculosis in the microplate alamar blue assay (MABA) with MIC = 23.7 μM, but also showed cytotoxicity (IC50 = 21.1 μM) in the vero cell test.
dc.identifier.citationGumula, I., Heydenreich, M., Derese, S., Ndiege, I. O., & Yenesew, A. (2012). Four isoflavanones from the stem bark of Platycelphium voënse. Phytochemistry Letters, 5(1), 150-154.
dc.identifier.otherhttps://doi.org/10.1016/j.phytol.2011.11.012
dc.identifier.urihttps://nru.uncst.go.ug/handle/123456789/9999
dc.language.isoen
dc.publisherPhytochemistry Letters
dc.titleFour isoflavanones from the stem bark of Platycelphium voe¨nse
dc.typeArticle

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