Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/1118
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dc.contributor.authorWanjala, Cornelius C.-
dc.contributor.authorBojase, Gomotsang-
dc.contributor.authorMajinda, Runner R. T.-
dc.date.accessioned2015-03-31T08:50:00Z-
dc.date.available2015-03-31T08:50:00Z-
dc.date.issued2001-
dc.identifier.citationBu ll. Chem. Soc. Eth iop. 2001, 15(2), 131-136en_US
dc.identifier.issn1011-3924-
dc.identifier.urihttp://www.ajol.info/index.php/bcse/article/view/20958/3902-
dc.identifier.urihttp://repository.seku.ac.ke/handle/123456789/1118-
dc.description.abstractThe structures of two new isoflavonoids from the combined ethyl acetate/methanolic extracts of the stem bark of Bolusanthus speciosus have been established as 4,7,2' -trihydroxy-4' -methoxyisoflavanol (1) and 5,7,3' ,4' -tetrahydroxy-5' -(2-epoxy-3-methylbutyl)isoflavanone (2). Five other known isoflavonoids, 5,7,3' -trihydroxy-4' -methoxy-5' -γγ; -dimethylallylisoflavanone, 5,7,2' -trihydroxy-4' -methoxy-6,5' -di)(γγ -dimethylallyl)isoflavanone, 5,7,2' ,4'-tetrahydroxy-8,5'2; -di(γγ -dimethylallyl)flavanone, 5,7,2' ,4' -tetrahydroxy-8,3' -di(γγ -dimethylallyl)-isoflavanone, and derrone were also isolated. Compound 2 showed moderate activity against gram positive bacteria and weak activity against gram negative bacteria, while compound 1 was weakly active against both organisms in a TLC bioautography assay.en_US
dc.language.isoenen_US
dc.subjectBolusanthus speciosusen_US
dc.subject4,7,2¢-Trihydroxy-4¢-methoxyisoflavanolen_US
dc.subject5,7,3¢,4¢- Tetrahydroxy-5¢-(2-epoxy-3-methylbutyl)isoflavanoneen_US
dc.subjectAntibacterial activityen_US
dc.titleTwo new isoflavanoids from Bolusanthus Speciosusen_US
dc.typeArticleen_US
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