Show simple item record

dc.contributor.authorMuhammada, Ilias
dc.contributor.authorWalkera, Larry A.
dc.contributor.authorHester, John P.
dc.contributor.authorMidiwob, Jacob O.
dc.contributor.authorJacoba, Melissa R.
dc.contributor.authorKhana, Shabana I.
dc.contributor.authorTekwania, Babu L.
dc.contributor.authorJaina, Surendra K.
dc.contributor.authorSamoylenkoa, Volodymyr
dc.contributor.authorRahmana, Aziz A.
dc.date.accessioned2013-06-28T08:32:33Z
dc.date.available2013-06-28T08:32:33Z
dc.date.issued2011
dc.identifier.citationNatural Product Communications Vol. 6 (11) 2011en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/41627
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 μg/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 μg/mL and 0.43 μg/mL, respectively, against L. donovani promastigotes. Both the compounds were also evaluated against L. donovani axenic amastigotes and amastigotes in THP1 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 μg/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.subjectAbrus schimperi, Amorphaquinone, Pendulone, NMR, Circular Diachroism, Antimicrobial, Antiparasitic, Cytotoxic.en
dc.titleNPC Natural Product Communicationsen
dc.typeArticleen
local.publisherDepartment of Chemistry, University of Nairobi,en
local.publisherNational Center for Natural Products Research and cDepartment of Pharmacology, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, Mississippien


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