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A prenylated cinnamaldehyde (glomeral), together with the known p -hydroxycinnamic acid, caffeic acid, methyl cinnamate, hesperetin, scoparone, skimmianine, syringaresinol and two limonoids (limonin and limonyl acetate) were isolated from the roots and stem bark of Vepris glomerata . The antibacterial assay of the isolated compounds indicated an inhibition zone, ranging from 8 to 16 mm, against standard strains of Staphylococcus aureus (ATCC 29213, 25923) and Shigella dysentrieae . Glomeral inhibited the growth of S. aureus and S. dysentrieae at low concentrations (MIC of 2 μg/mL and 0.4 μg/mL respectively). Of the other compounds tested, hesperetin displayed good antibacterial activity, the limonoids, scoparone and skimmianine displayed moderate antibacterial activity and the cinnamic acid derivatives were inactive against the test pathogens. This study provides a rationale for the use of V. glomerata in its treatment of bacterial infections.

Two A-seco-limonoids, accorded the trivial names, uguenensene and uguenensone and a C-7 prenylated flavonoid, uguenenprenol were isolated from Vepris uguenensis (Rutaceae). In addition, 11 known compounds, niloticin, chisocheton A, kihadalactone A, limonyl acetate, methyl uguenenoate, 7-O-methylaromadenrin, flindersiamine, 8α,11-elemodiol, tricoccin S₁₃ acetate, skimmianine, and lupeol were isolated. The structures of the compounds were elucidated and characterized by spectroscopic analyses (NMR, GC-MS and IR). Antioxidant activity of the isolated compounds showed that uguenenprenol and 7-O-methylaromadenrin are good antioxidant agents. Significantly high antioxidant activity was also exhibited by 8α,11-elemodiol, which was 72% at 250 μg mL⁻¹ and 57% at 15.62 μg mL⁻¹ when tested with the deoxyribose method. The two liminoids fit nicely into the biosynthetic pathway from niloticin to methyl uguenenoate.

The present study was conducted to examine the anti-oxidative activities of extracts from different parts of Ziziphus mucronata. Stem bark, root and leaf samples were sequentially extracted with solvents of increasing polarity and tested for in vitro anti-oxidative activity using various models. Our results indicated that all the extracts had potent electron donating and 1,1-diphenyl-2-picryl-hydrazyl (DPPH) radical scavenging activities. However, the ethanolic extracts exhibited a significantly (p

Hydro-distilled essential oil from Satureja biflora (Lamiaceae) growing in Kenya was analysed by gas chromatography mass spectrometry (GC-MS) and also evaluated for antimicrobial activity. Twenty two compounds which constitute 99.29 % of the total oil were identified. The oil was dominated by monoterpenes, which accounted for 62.02 % of the oil. This monoterpene fraction was characterized by a high percentage of linalool (50.60 %) such that this Satureja species can be classified as the linalool chemotype. The other major monoterpenes were α-terpineol (2.80 %), β-ocimene (2.25 %), β-pinene (1.96 %) and cis -linalool oxide (1.91 %). Sesquiterpenes present in fairly good amounts are germacrene D (10.63 %), α-cadinol (4.53 %), β-bourbonene (2.33 %), δ-cadinene (2.19 %), τ-cadinol (2.17 %), endo-1-bourbonanol (2.14 %) and β-caryophyllene (1.98 %). Aliphatic alcohols and acids accounted for 7.23 % of the oil, of which the major one was linoleic acid (4.48 %). The oil was screened for antimicrobial activity against both gram-positive ( Staphylococcus aureus, Bacillus ssp. ) and gram-negative ( Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, Klebsiella pheumoniae, Proteus mirabilis ) bacteria and a pathogenic fungus ( Candida albicans ). To the best of our knowledge nothing concerning the chemical composition and biological activity of the essential oil of S. biflora has been reported. KEY WORDS : Satureja biflora , Essential oil, Antimicrobial activity Bull. Chem. Soc. Ethiop. 2007 , 21(2), 249-254.