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dc.contributor.authorTsegaye, Deyou
dc.contributor.authorMakungu, Marco
dc.contributor.authorMatthias, Heydenreich
dc.contributor.authorPan, Fangfang
dc.contributor.authorAmra, Gruhonjic
dc.contributor.authorFitzpatrick, Paul A.
dc.contributor.authorAndreas, Koch
dc.contributor.authorSolomon, Derese
dc.contributor.authorJerry, Pelletier
dc.contributor.authorRissanen, Kari
dc.contributor.authorAbiy, Yenesew
dc.contributor.authorMáté, Erdélyi
dc.date.accessioned2019-09-10T09:53:42Z
dc.date.available2019-09-10T09:53:42Z
dc.date.issued2017
dc.identifier.citationDeyou, Tsegaye, et al. "Isoflavones and Rotenoids from the Leaves of Millettia oblata ssp. teitensis." Journal of natural products 80.7 (2017): 2060-2066.en_US
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.jnatprod.7b00255
dc.identifier.urihttps://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.7b00255?rand=rz0pql5q
dc.identifier.urihttp://erepository.uonbi.ac.ke/handle/11295/107094
dc.description.abstract: A new isoflavone, 8-prenylmilldrone (1), and four new rotenoids, oblarotenoids A−D (2−5), along with nine known compounds (6−14), were isolated from the CH2Cl2/CH3OH (1:1) extract of the leaves of Millettia oblata ssp. teitensis by chromatographic separation. The purified compounds were identified by NMR spectroscopic and mass spectrometric analyses, whereas the absolute configurations of the rotenoids were established on the basis of chiroptical data and in some cases by single-crystal X-ray crystallography. Maximaisoflavone J (11) and oblarotenoid C (4) showed weak activity against the human breast cancer cell line MDA-MB-231 with IC50 values of 33.3 and 93.8 μM, respectively.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.titleIsoflavones and Rotenoids from the Leaves of Millettia oblata ssp. teitensisen_US
dc.typeArticleen_US


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