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dc.contributor.authorYenesew Abiy.
dc.contributor.authorInduli Martha.
dc.contributor.authorDerese Solomon.
dc.contributor.authorMidiwo Jacob O.
dc.contributor.authorHeydenreich Matthias.
dc.contributor.authorPeter Martin G
dc.contributor.authorAkala Hoseah.
dc.contributor.authorWangui Julia.
dc.contributor.authorLiyala Pamela.
dc.contributor.authorWaters Norman C.
dc.date.accessioned2013-07-03T09:20:56Z
dc.date.available2013-07-03T09:20:56Z
dc.date.issued2004
dc.identifier.citationAbiy Yenesew, Martha Induli, Solomon Derese et al (2004). Anti-plasmodial flavonoids from the stem bark of Erythrina abyssinica. Phytochemistry Volume 65, Issue 22, November 2004, Pages 3029–3032en
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S003194220400442X
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/44548
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/15504437
dc.description.abstractThe ethyl acetate extract of the stem bark of Erythrina abyssinica showed anti-plasmodial activity against the chloroquine-sensitive (D6) and chloroquine-resistant (W2) strains of Plasmodium falciparum with IC50 values of 7.9 ± 1.1 and 5.3 ± 0.7 μg/ml, respectively. From this extract, a new chalcone, 2′,3,4,4′-tetrahydroxy-5-prenylchalcone (trivial name 5-prenylbutein) and a new flavanone, 4′,7-dihydroxy-3′-methoxy-5′-prenylflavanone (trivial name, 5-deoxyabyssinin II) along with known flavonoids have been isolated as the anti-plasmodial principles. The structures were determined on the basis of spectroscopic evidence.en
dc.language.isoenen
dc.titleAnti-plasmodial flavonoids from the stem bark of Erythrina abyssinicaen
dc.typeArticleen
local.publisherDepartment of Chemistry, University of Nairobien
local.publisherInstitut für Chemie, Universität Potsdam, Germanyen
local.publisherUnited States Army Medical Research Unit-Kenya, USAen


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