Show simple item record

dc.contributor.authorInduli, M
dc.contributor.authorGebru, M
dc.contributor.authorAbdissa, N
dc.contributor.authorAkala, H
dc.contributor.authorWekesa, I
dc.contributor.authorByamukama, R
dc.contributor.authorHeydenreich, M
dc.contributor.authorMurunga, S
dc.contributor.authorDagne, E
dc.contributor.authorYenesew, A.
dc.date.accessioned2014-03-06T10:55:54Z
dc.date.available2014-03-06T10:55:54Z
dc.date.issued2013-09
dc.identifier.citationNat Prod Commun. 2013 Sep;8(9):1261-4en_US
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/24273862
dc.identifier.urihttp://hdl.handle.net/11295/65107
dc.description.abstractExtracts of the rhizomes of Kniphofia foliosa exhibited antiplasmodial activities against the chloroquine-sensitive (D6) and chloroquine-resistant (W2) strains of Plasmodium falciparum with IC50 values of 3-5 microg/mL. A phenyloxanthrone, named 10-acetonylknipholone cyclooxanthrone (1) and an anthraquinone-anthrone dimer, chryslandicin 10-methyl ether (2), were isolated from the rhizomes, along with known quinones, including the rare phenylanthraquinone dimers, joziknipholones A and B. The structures of these compounds were determined based on spectroscopic data. This is the second report on the occurrence of the dimeric phenylanthraquinones in nature. In an in vitro antiplasmodial assay of the isolated compounds, activity was observed for phenylanthraquinones, anthraquinone-anthrone dimers and dimeric phenylanthraquinones, with joziknipholone A being the most active. The new compound, 10-acetonylknipholone cyclooxanthrone, also showed anti-plasmodial activity. In an in vivo assay, knipholone anthrone displayed marginal antimalarial activity.en_US
dc.language.isoenen_US
dc.titleAntiplasmodial quinones from the rhizomes of Kniphofia foliosa.en_US
dc.typeArticleen_US


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record