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dc.contributor.authorAkimanya, Aggrey
dc.contributor.authorMidiwo, Jacob O.
dc.contributor.authorOkanga, Francis
dc.contributor.authorKerubo, Leonidah
dc.contributor.authorIlias, Muhammad
dc.contributor.authorWalker, Larry
dc.date.accessioned2015-11-05T09:55:00Z
dc.date.available2015-11-05T09:55:00Z
dc.date.issued2015
dc.identifier.citationAkimanya, Aggrey., Midiwo, Jacob O., Okanga, Francis., Kerubo, Leonidah., Ilias, Muhammad and Walker, Larry. (2015). Two flavonoids and a rearranged clerodane diterpenoid from the leaf exudates of microglossa pyrifolia. The 16th symposium of the natural products reseach network for eastern and central Africa (NAPRECA) 31st August to 3rd September 2015 Arusha, Tanzaniaen_US
dc.identifier.urihttp://www.napreca-tz.org/16napreca/16th_NAPRECA_Book_Abstracts.pdf
dc.identifier.urihttp://hdl.handle.net/11295/92282
dc.description.abstractThe fresh leaves of Microglossa pyrifolia , Asteraceae (7.5 kg) were extracted by successive dipping into fresh portions of ethyl acetate for short periods (less than or ca. 15 s) to yield (180 g, 2.4% of dry leaf) of yellow concentrate. The crude extr act was found to have IC50 of 8.0 μg/ml against P.falciparum D6 strain and 13.0 μg/ml against W2. A portion of the crude extract (150 g) was subjected to column chromatography on silica gel (1500 g) eluting with mixtures of n - hexane/CH 2 Cl 2 and then with CH 2 Cl 2 /MeOH in increasing polarities. A total of seven compounds (two diterpenoids and five fl avonoids),whose structures were determined using NMR (1H, 13C, COSY, HMQC , and HMBC) and EIMS as 5,7,4 - trihydro xy - 3,8,3 - t rimethoxyflavone (1), 5, 7, 4 - trihydroxy - 3, 8, 3, 5 - tetramethoxyflavone (2), 5,3,4 - trihydroxy - 7 - methoxyflavanone (3), 5,7,3 - trihydroxy - 8,4,5 - trimethoxyflavone (4), 5, 3, 4 - Trihydroxy - 3, 7, 8 - trimethoxyflavone (5) 8 - acetoxyisochiliolide lactone (6) and 7, 8 - epoxyisocholiolide lactone (7); out of the se 2,4 and 6 were new to literature. Tests with DPPH showed that antioxidant activity was e xhibited by 1 with IC50 of 6.2 μg/ml. Compound 6 exhibited modest in vitro antileishmanial activity with IC 50 value of 13.13 mg/mL against the growth of Leish mania d onovanii promastigotesen_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.titleTwo flavonoids and a rearranged clerodane diterpenoid from the leaf exudates of microglossa pyrifoliaen_US
dc.typePresentationen_US
dc.type.materialenen_US


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