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Antimycobacterial and cytotoxicity evaluation of the constituents of Monodora carolinae

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dc.creator Magoria, Nyangi
dc.creator Nyandoro, Stephen S.
dc.creator Munissi, Joan J. E.
dc.creator Heydenreichb, Matthias
dc.date 2016-06-26T17:08:50Z
dc.date 2016-06-26T17:08:50Z
dc.date 2013
dc.date.accessioned 2018-03-27T08:54:41Z
dc.date.available 2018-03-27T08:54:41Z
dc.identifier 0856 1761
dc.identifier http://hdl.handle.net/20.500.11810/2672
dc.identifier.uri http://hdl.handle.net/20.500.11810/2672
dc.description Phytochemical investigation of the stem bark of the recently described species Monodora carolinae (Annonaceae) afforded prenylindole derivatives (E)-4-(1H-indol-6-yl)-but-3-en-2-one (1), 5-formylindole (2), fatty acid (Z)-hexade-7-enoic acid (3) and the lignanamide cannabisin B (4). The structures of the isolated compounds were established using NMR and MS analyses. The antimycobacterial activities of the extracts and isolated compounds were evaluated against Mycobacterium madagascariense (MM) and M. indicus pranii (MIP) using the two-fold microtitre dilution method. While the extracts exhibited minimum inhibitory concentration (MIC) ranging from 500 – 1000 ìg/mL, the isolated compounds were 125 – 250 ìg/mL, indicating very low activity. Cytotoxic effects were evaluated using brine shrimp larvae whereby the ethanolic extract of the root bark exhibited the lowest LC50 (< 3ìg/mL). Isolation of prenylindole derivatives is of chemotaxonomic significance that affirms taxonomic placement of this plant species into the genus Monodora. This is the first time cannabisin B is reported from the genus Monodora.
dc.language en
dc.subject Monodora carolinae
dc.subject Annonaceae
dc.subject Prenylindole
dc.subject Cannabisin B
dc.subject (Z)-hexade-7-enoic acid
dc.subject Antimycobacterial
dc.subject Cytotoxicity
dc.title Antimycobacterial and cytotoxicity evaluation of the constituents of Monodora carolinae
dc.type Journal Article, Peer Reviewed


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