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dc.contributor.authorYenesew Abiy.
dc.contributor.authorMushibe,EK.
dc.contributor.authorInduli M.
dc.contributor.authorDerese Solomon.
dc.contributor.authorMidiwo Jacob O.
dc.contributor.authorKabaru JM.
dc.contributor.authorHeydenreich M.
dc.contributor.authorKoch A.
dc.contributor.authorPeter MG.
dc.date.accessioned2013-06-15T12:02:19Z
dc.date.available2013-06-15T12:02:19Z
dc.date.issued2005-03
dc.identifier.citationPhytochemistry Volume 66, Issue 6, March 2005, Pages 653–657en
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0031942205000579
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/34454
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/15771885
dc.description.abstractFrom the acetone extract of the roots of Derris trifoliata an isoflavonoid derivative, named 7a-O-methyldeguelol, a modified rotenoid with an open ring-C, representing a new sub-class of isoflavonoids (the sub-class is here named as rotenoloid), was isolated and characterised. In addition, the known rotenoids, rotenone, deguelin and α-toxicarol, were identified. The structures were determined on the basis of spectroscopic evidence. Rotenone and deguelin were identified as the larvicidal principles of the acetone extract of the roots of Derris trifoliata.en
dc.language.isoenen
dc.subjectDerris trifoliataen
dc.subjectLeguminosaeen
dc.subjectRootsen
dc.subjectRotenoidsen
dc.subjectRotenoloiden
dc.subject7a-O-methyldeguelolen
dc.subjectConformationen
dc.subjectEnergy calculationen
dc.subjectMosquitoen
dc.subjectLarvicidesen
dc.subjectCulex quinquefasciatusen
dc.title7a-O-methyldeguelol, a modified rotenoid with an open ring-C, from the roots of Derris trifoliataen
dc.typeArticleen
local.publisherDepartment of Chemistry, University of Nairobien
local.publisherDepartment of Zoology, University of Nairobi,en
local.publisherInstitut für Chemie, Universität Potsdam, P.O. Box 601553, D-14415 Potsdam, Germanyen


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