2 research outputs found

    Lesser Known Aromatic Plants in Nigeria

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    Herbs and spices are used in all cultures as natural foodstuffs and for medicinal purposes. Siphonochilus aethiopicus, Monodora myristica and Crateva adansonii are some of the spices which are not commonly used. They improve the taste of food, and through their anti-oxidant, anti-microbial and anti-fungal properties, they could act as food preservatives. There is an accumulation of evidence for the usage of these spices medicinally as anti-inflammatory, anti-plasmodial, anti-sickling, anti-oxidant and chemopreventive agents. There have also been investigations to identify the active constituents of these spices and to verify their pharmacological actions. This article aims at reviewing the available data on these investigations and the basis for usage in several diseases and conditions

    Two new antiprotozoal diterpenes from the roots of Acacia nilotica

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    The powdered roots of the medicinal plant Acacia nilotica were extracted with hexane and ethyl acetate, and the extracts were subjected to column chromatography for the isolation of potentially bioactive compounds and their screening against kinetoplastid pathogens. NMR and HREI mass spectrometric analyses identified two new diterpenes, characterized as 16, 19-dihydroxycassa-12-en-15-one (Sandynone, 1) and (5S, 7R, 8R, 9R, 10S, 13Z, 17S)-7,8:7,17:16,17-triepoxy-7,8-seco-cassa-13-ene (niloticane B, 2). The previously reported (5S,7R,8R,9R,10S) -(-)-7,8-seco-7, 8-oxacassa-13,15-diene-7,17-diol (3), (5S,7R,8R,9R,10S) -(-)-7,8-seco-7, 8-oxacassa-13,15-dien-7-ol-17-al (4), and (5S,7R,8R,9R,10S) -(-)-7,8-seco-7, 8-oxacassa-13,15-dien-7-ol (5) a, mixture of stigmasterol (6a) and sitosterol (6b), and lupeol (7) were also isolated. Several column fractions displayed significant activity against a panel of Trypanosoma and Leishmania spp., and from the most active fraction, compound 4 was isolated with high purity. The compound displayed high activity, particularly against T. brucei, T. evansi, and L. mexicana (0.88–11.7 µM) but only a modest effect against human embryonic kidney cells and no cross-resistance with the commonly used melaminophenyl arsenical and diamidine classes of trypanocides. The effect of compound 4 against L. mexicana promastigotes was irreversible after a 5-h exposure, leading to the sterilization of the culture between 24 and 48 h
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