dc.contributor.author | Ivan Gumula | |
dc.contributor.author | Matthias Heydenreich | |
dc.contributor.author | Solomon Derese | |
dc.contributor.author | Isaiah Omolo Ndiege | |
dc.contributor.author | Abiy Yenesew | |
dc.date.accessioned | 2021-01-10T11:55:38Z | |
dc.date.available | 2021-01-10T11:55:38Z | |
dc.date.issued | 2012 | |
dc.identifier.issn | 18743900 | |
dc.identifier.uri | https://combine.alvar.ug/handle/1/49043 | |
dc.description.abstract | Abstract From the stem bark of Platycelphium voense (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 (IC 50 = 21.1 μM) in the vero cell test. | |
dc.publisher | Elsevier BV | |
dc.relation.ispartof | Phytochemistry Letters | |
dc.title | Four Isoflavanones from the stem bark of Platycelphium voënse. | |
dc.type | journal article | |
dc.identifier.doi | 10.1016/j.phytol.2011.11.012 | |
dc.identifier.mag | 2017162692 | |
dc.identifier.lens | 027-006-712-883-954 | |
dc.identifier.volume | 5 | |
dc.identifier.issue | 1 | |
dc.identifier.spage | 150 | |
dc.identifier.epage | 154 | |
dc.subject.lens-fields | Cytotoxicity | |
dc.subject.lens-fields | Flavones | |
dc.subject.lens-fields | Formononetin | |
dc.subject.lens-fields | Betulin | |
dc.subject.lens-fields | Kumatakenin | |
dc.subject.lens-fields | Antibacterial activity | |
dc.subject.lens-fields | Amyrin | |
dc.subject.lens-fields | Terpene | |
dc.subject.lens-fields | Stereochemistry | |
dc.subject.lens-fields | Biology |
|