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dc.contributor.authorRahman AA.
dc.contributor.authorSamoylenko V.
dc.contributor.authorJain SK.
dc.contributor.authorTekwani BL.
dc.contributor.authorKhan SI.
dc.contributor.authorJacob MR.
dc.contributor.authorMidiwo Jacob O.
dc.contributor.authorHester JP.
dc.contributor.authorWalker LA.
dc.contributor.authorMuhammad I.
dc.date.accessioned2013-06-21T06:24:15Z
dc.date.available2013-06-21T06:24:15Z
dc.date.issued2011-11
dc.identifier.citationNat Prod Commun. 2011 Nov;6(11):1645-50.en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/22224279
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/37122
dc.description.abstractThe EtOH extract of Abrus schimperi (Fabaceae), collected in Kenya, demonstrated significant activity against Leishmania donovani promastigotes with IC50 value of 3.6 microg/mL. Bioassay-guided fractionation of CHCl3 fraction using Centrifugal Preparative TLC afforded two antiparasitic isoflavanquinones, namely amorphaquinone (1) and pendulone (2). They displayed IC50 values of 0.63 microg/mL and 0.43 microg/mL, respectively, against L. donovani promastigotes. Both the compounds were also evaluated against L. donovani axenic amastigotes and amastigotes in THPI macrophage cultures. In addition, compounds 1 and 2 showed antiplasmodial activity against Plasmodium falciparum D6 and W2 strains, while 2 displayed antibacterial activity against Staphylococcus aureus and methicillin-resistant S. aureus (each IC50 1.44 microg/mL). The 1H and 13C data of 1, not fully assigned previously, were unambiguously assigned using 1D and 2D NMR HMBC and HMQC experiments. In addition, the absolute stereochemistry of the isolated compounds 1 and 2 was revised as C-(3S) based on Circular Dichroism experiments. This appears to be the first report of amorphaquinone (1) and pendulone (2) from the genus Abrus.en
dc.language.isoenen
dc.titleAntiparasitic and antimicrobial isoflavanquinones from Abrus schimperi.en
dc.typeArticleen


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