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dc.contributor.authorDeyou, T
dc.contributor.authorMarco, M
dc.contributor.authorHeydenreich, M
dc.contributor.authorPan, F
dc.contributor.authorGruhonjic, A
dc.contributor.authorFitzpatrick, PA
dc.contributor.authorKoch, A
dc.contributor.authorDerese, S
dc.contributor.authorPelletier, J
dc.contributor.authorRissanen, K
dc.contributor.authorYenesew, A
dc.contributor.authorErdélyi, M
dc.date.accessioned2017-10-18T07:23:01Z
dc.date.available2017-10-18T07:23:01Z
dc.date.issued2017
dc.identifier.citationJ Nat Prod. 2017 Jul 28;80(7):2060-2066. doi: 10.1021/acs.jnatprod.7b00255. Epub 2017 Jun 30.en_US
dc.identifier.urihttp://pubs.acs.org/doi/abs/10.1021/acs.jnatprod.7b00255
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/28665590
dc.identifier.urihttp://hdl.handle.net/11295/101130
dc.description.abstractA 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. Teitensis.en_US
dc.typeArticleen_US


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