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dc.contributor.authorKuria, KA
dc.contributor.authorChepkwony, H
dc.contributor.authorGovaerts, C
dc.contributor.authorRoets, E
dc.contributor.authorBusson, R
dc.contributor.authorDe Witte, P
dc.contributor.authorZupko, I
dc.contributor.authorHoornaert, G
dc.contributor.authorQuirynen, L
dc.contributor.authorMaes, L
dc.contributor.authorJanssens, L
dc.contributor.authorHoogmartens, J
dc.contributor.authorLaekeman, G
dc.date.accessioned2013-06-06T13:11:41Z
dc.date.available2013-06-06T13:11:41Z
dc.date.issued2002-05
dc.identifier.citationJ Nat Prod. 2002 May;65(5):789-93.en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/12027771
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/29313
dc.description.abstractAjuga remota is the most frequently used medicinal herb for malaria treatment in Kenya. Its two known isolates ajugarin-1 (1) and ergosterol-5,8-endoperoxide (3) and a new isolate 8-O-acetylharpagide (2) were evaluated for their in vitro antiplasmodial activity. Ajugarin-1 was moderately active, with an IC(50) of 23.0 +/- 3.0 microM, as compared to chloroquine (IC(50) = 0.041 +/- 0.003 microM) against the chloroquine-sensitive (FCA 20/GHA) strain of Plasmodium falciparum. Ergosterol-5,8-endoperoxide was about 3x as potent (IC(50) = 8.2 +/- 1.1 microM), while 8-O-acetylharpagide, whose structure was established by spectroscopic evidence, was inactive. Both ajugarin-1 and ergosterol-5,8-endoperoxide did not exhibit cytotoxicity against A431 (skin carcinoma) cell line, but 8-O-acetylharpagide was significantly cytotoxic. This iridoid glucoside, which has been formerly isolated from Ajuga decumbens, was identified in A. remota for the first time.en
dc.language.isoenen
dc.publisherUniversity of Nairobi.en
dc.titleThe antiplasmodial activity of isolates from Ajuga remotaen
dc.typeArticleen
local.publisherFaculty of Pharmacy, University of Nairobien


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