Browsing Research articles (Dept of Chemistry) by Author "Chacha, M."
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Chacha, M.; Mapitse, R.; Afolayan, AJ; Majinda, R.R.T. (Natural Product Inc. http://www.naturalproduct.us/, NaN, 2008)[more][less]
Abstract: Investigation of the roots of Ceriops tagal led to the isolation of a new isopimarane, together with the known diterpenes isopimar-8(14)-en-15,16-diol and erythroxyl-4(17),15(16)-dien-3-one. The structure of the new compound was identified as isopimar-8(14)-en-16-hydroxy-15-one. These structures were determined from extensive spectroscopic data analysis. The isolates were screened for antibacterial activity using the agar dilution method against ten test bacterial strains (Bacillus cereus, Escherichia coli, Klebsiella pneumoniae, Micrococcus kristinae, Pseudomonas aeruginosa, Salmonella pooni, Serratia marcescens, Staphylococcus aureus, S. epidermidis and Streptococcus pyrogens). Isopimar-8(14)-en-16-hydroxy-15-one exhibited activity, with MIC values of 0.5 mg/mL against Streptococcus pyrogens; 0.25 mg/mL against Salmonella pooni and 0.1 mg/mL against Bacillus cereus, Staphylococcus aureus and Micrococcus kristinae. URI: http://hdl.handle.net/10311/224 Files in this item: 2
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Chacha, M.; Bojase-Moleta, G.; Majinda, R.R.T. (Elsevier Ltd; http://www.elsevier.com/wps/find/journaldescription.cws_home/273/description, November 20, 2004)[more][less]
Abstract: From the stem wood of Erythrina latissima, two isoflavones and a flavanone were isolated and characterized as 7,3'-dihydroxy-4'-methoxy-5'-(y,y-dimethylallyl)isoflavone (erylatissin A), 7,3'-dihydroxy-6".6"-dimethyl-4".5"-dehydropyrano [2",3":4'.5']isoflavone (erylatissin B), (-)-7,3'-dihydroxy-4'-methoxy-5'-(y,y-dimethylallyl)flavanone (erylatissin C), respectively, in addition to 10 known flavonoids. Structures of these compounds were determined on the basis of their spectroscopic data. These compounds showed antimicrobial activity against Escherichia coli, Staphylococcus aureus, Bacillus subtilis and Candida mycoderma. The isolated compounds also exhibited weak radical scavenging properties towards DPPH radical. URI: http://hdl.handle.net/10311/216 Files in this item: 2
license.txt (1.998Kb)
Now showing items 1-2 of 2