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dc.contributor.authorMachumi F.
dc.contributor.authorYenesew Abiy.
dc.contributor.authorMidiwo Jacob O.
dc.contributor.authorHeydenreich M.
dc.contributor.authorKleinpeter E.
dc.contributor.authorKhan S.
dc.contributor.authorTekwani BL.
dc.contributor.authorWalker LA.
dc.contributor.authorMuhammad I.
dc.date.accessioned2013-06-21T06:17:10Z
dc.date.available2013-06-21T06:17:10Z
dc.date.issued2012-09
dc.identifier.citationPlanta Med 2012; 78 - PI255en
dc.identifier.urihttps://www.thieme-connect.com/ejournals/abstract/10.1055/s-0032-1320942
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/37112
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/23074885
dc.description.abstractThe 1:1 MeOH/CH2Cl2 extract of aerial parts of Sphaeranthus bullatus, an annual herb native to tropical East Africa, showed activity against chloroquine sensitive D6 (IC50 9.7µg/ml) and chloroquine resistant W2 (IC50 15.0µg/ml) strains of P. falciparum. Seventeen secondary metabolites were isolated and evaluated for their in-vitro antiplasmodial, antileishmanial and anticancer activities revealing activity on four carvotacetone derivatives 1-4; with antiplasmodial activity of IC50 3.4, 0.6, 0.8, 1.4µg/ml respectively against D6 strains of P. falciparum; antiplasmodial activity of IC50 2.8, 0.7, 0.9, 2.0µg/ml respectively against W2 strains of P. falciparum; antileishmanial activity of IC50 17.0, 0.7, 3.0 and 0.7 respectively against the parasite L. donovanii, and anticancer activity of IC50 <5.3µg/ml against SK-MEL, KB, BT-549 and SK-OV-3 cells for 2-4. In addition, cytotoxicity of the active compounds was evaluated against monkey kidney fibroblasts (VERO) and pig kidney epithelial (LLC-PK11) cells.en
dc.language.isoenen
dc.titleAntiparasitic and anticancer carvotacetone derivatives from Sphaeranthus bullatusen
dc.typeArticleen
local.publisherDepartment of Chemistry, University of NairobIen


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