Browsing by Author "Abegaz, B.M."
Now showing items 1-17 of 17
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Kouam, S.F.; Flo¨rke, U.; Krohn, K.; Akhtar, M.N.; Ngadjui, B.T.; Abegaz, B.M. (February 13, 2009)[more][less]
Abstract: Isolation of the title compound, C30H50O, from Bridelia micrantha yielded suitable crystals for an X-ray structure determination, showing it to be in the -form. The crystal packing is determined by infinite zigzag O—H O hydrogenbonded chains. URI: http://hdl.handle.net/10311/285 Files in this item: 1
Taraxerol.pdf (955.6Kb) -
Kuete, V.; Ngameni, B.; Tsafack, A.M.; Ambassa, P.; Simo, I.K.; Bezabih, M.; Etoa, F.; Ngadjui, BT; Abegaz, B.M.; Beng, V.P. (Pharmacologyonline. http://www.pharmacologyonline.org/, NaN, 2007)[more][less]
Abstract: The crude extract from the twigs of Dorstenia elliptica (DET) as well one of the five compounds isolated from this extract namely O-[3-(2, 2-dimethyl-3-oxo-2H-furan-5-yl)-3- hydroxybutyl]bergaptol (5) were tested for their antimicrobial activity against bacteria and fungi. The Agar disc diffusion test was used to determine the sensitivity of the tested samples while the well micro-dilution was used to determine the minimal inhibition concentrations (MIC) and the minimal microbicidal concentration (MMC) of the active samples. The results of the disc diffusion assay showed that DET prevented the growth of all the 22 tested microbial species while the two tested compounds showed selective activity. At the tested MIC interval ranged from 1.22 to 156.25 μg/ml for the crude extracts and 0.08 to 39.06 μg/ml for the compounds, the activity of DET was noted on 20 of the 22 microbial species. The antimicrobial activities of DET as well as that compound 5 are being reported for the first time. The overall results provide promising baseline information for the potential use of the crude extract in the treatment of bacterial and fungal infections. URI: http://hdl.handle.net/10311/287 Files in this item: 1
ANTIMICROBIAL ACTIVITY OF THE.pdf (4.398Mb) -
Kuete, V.; Metuno, R.; Ngameni, B.; Tsafack, A.M.; Ngandeu, F.; Fotso, G.W.; Bezabih, M.; Etoa, F.; Ngadjui, B.T.; Abegaz, B.M.; Penlap, B.V. (Elsevier Ireland Ltd. www.elsevier.com/locate/jethpharm, NaN, 2007)[more][less]
Abstract: The crude extract from Treculia obovoidea was subjected to purification by repeated chromatography. Eight compounds were isolated from Treculia obovoidea and identified as Psoralen (1), Bergapten (2), 7-methoxycoumarin (3), 7-hydroxycoumarin (4), 4,2 ,4 -trihydroxychalcone (5), 4,2 ,4 -trihydroxy-3-prenylchalcone (6), 3-hydroxy-4-methoxybenzoic acid (7) and O-[3-(2,2-dimethyl-3-oxo-2H-furan-5-yl) butyl] bergaptol (8). These compounds together with the extract were tested for their antimicrobial activity against Gram-positive bacteria (six species), Gram-negative bacteria (12 species) and three Candida species using micro-dilution methods for the determination of the minimal inhibition concentration (MIC) and the minimal microbicidal concentration (MMC). The MIC values obtained with the crude extracts varied from 78.12 to 156.25 g/ml against 17 (80.95%) of the 21 tested microorganisms. All the isolated compounds showed selective activity. The antimicrobial activity of this plant as well as that of compounds 6 and 8 is being reported for the first time. The obtained results provide promising baseline information for the potential use of these crude extract as well as some of the isolated compounds in the treatment of bacterial and fungal infections. URI: http://hdl.handle.net/10311/288 Files in this item: 1
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Omisore, N.O.A.; Adewunmi, C.O.; Iwalewa, E.O.; Ngadjui, B.T.; Adenowo, T.K.; Abegaz, B.M.; Ojewole, J.A.; Watchueng, J. (Brazilian Journal of Medical and Biological Research. http://www.scielo.br/scielo.php?pid=0100-879X&script=sci_serial, NaN, 2005)[more][less]
Abstract: Dorstenia barteri and D. convexa extracts and some isolated components of the former were investigated for effectiveness against Trichomonas gallinarum and compared with quercetin and quercitrin. The antioxidant activity of the extracts/compounds was also determined. The minimum lethal concentrations (MLCs) for the extract of D. barteri leaves and twigs at 24 h were found to be 15.625 and 15.625 μg/ml, respectively. However, the MLCs of the leaf and twig extract of D. convexa were 125 and 437.5 μg/ml, respectively. The prenylated and geranylated chalcones were as active as the prenylated flavones, 6- prenylapigenin and the diprenylated derivative 6,8-diprenyleridictyol. The order of the antitrichomonal activity of the compounds at 24 h was: quercetin (0.121 μg/ml) > quercitrin (0.244 μg/ml) ≥ bartericin B (0.244 μg/ml) > bartericin A (0.73 μg/ml) > stigmasterol (0.98 μg/ml) > 6,8-diprenyleridictyol = isobavachalcone = dorsmanin F (31.25 μg/ ml). D. barteri extracts, quercitrin, and bartericin A, and the prenylated flavonoids had potent antioxidant properties. The twig extract of D. barteri was more potent than the leaf extract. Moderate (EC50 >50 μg/ ml) and high (EC50 <50 μg/ml) antioxidant activities were detected in the leaf and twig extracts of D. barteri and the prenylated flavonoids. Prenylated flavonoids and the isolated compounds with antioxidant properties described here may account for the anti-inflammatory action of these extracts. The antitrichomonal and antioxidant activities shown by the extracts and compounds in this study are consistent with the ethnomedicinal and local use of the Dorstenia species studied. URI: http://hdl.handle.net/10311/284 Files in this item: 1
Antitrichomonal and antioxidant.pdf (2.508Mb) -
Masesane, I.B.; Yeboah, S.O.; Liebscher, J.; Mugge, C.; Abegaz, B.M. (Elsevier Science Ltd, http://www.elsevier.com/locate/phytochem, NaN, 2000)[more][less]
Abstract: The twigs of Rhus pyroides yielded a novel bichalcone 2',40,21-trihydroxy-4',41-dimethoxy-4-O-51-bichalcone. It was identified on the basis of spectroscopic data including 1D and 2D NMR spectroscopy. The name rhuschalcone-1 is proposed. URI: http://hdl.handle.net/10311/1028 Files in this item: 1
Masesane_P_2000.pdf (321.5Kb) -
Abegaz, B.M.; Ngadjui, B.T.; Dongo, E.; Ngameni, B.; Nindi, M.N.; Bezabih, M. (Elsevier Science Ltd. www.elsevier.com/locate/phytochem, NaN, 2002)[more][less]
Abstract: The twigs of Dorstenia prorepens furnished the digeranylated chalcone, 5,30-(3,7-dimethyl-2,6-octadienyl)-3,4, 20,40-tetrahydroxychalcone while Dorstenia zenkeri yielded the 30,40-(3-hydroxy-2,2-dimethyldihydropyrano)-4,20-dihydroxychalcone and a bichalcone. 4-Hydroxylonchocarpin was found in both plants. D. prorepens also yielded the known compounds: psoralen, bergapten, b-sitosterol and its D-glucopyranosyl derivative. D. zenkeri yielded p-hydroxybenzaldehyde, dorsmanin A, 4,20,40-trihydroxychalcone and 4,20,40-trihydroxy-30-prenylchalcone. Structures of the new compounds were established by UV, IR, MS and 2-D NMR analysis. URI: http://hdl.handle.net/10311/254 Files in this item: 2
Chalcones and other constituents.pdf (3.760Mb)license.txt (1.998Kb) -
Metuno, R.; Ngandeu, F.; Tchinda, A.T.; Ngameni, B.; Kapche, G.D.W.F.; Djemgou, P.C.; Ngadjui, B.T.; Bezabih, M.; Abegaz, B.M. (Elsevier Ltd. www.elsevier.com/locate/biochemsyseco, NaN, 2007)[more][less]
Abstract: Three species of the genus Treculia namely, Treculia acuminata Baill., Treculia africana Decne ex. Treà ´cul and Treculia obovoidea N.E.Br. grow in the humid rain forest of southwest Cameroon. They are also widely distributed in tropical Africa. T. africana is commonly known as African bread fruit. These three species are commonly used in folk medicine against skin diseases and dental allergies (Berg et al., 1985). The twigs, stem and wood of T. acuminata and the leaves of T. africana, whose chemical constituents are reported herein, were collected from Kumba, Cameroon, in August 2004, and identified by Mr Victor Nana of the National Herbarium in Yaounde, Cameroon where voucher specimens (N 2921/Srf/CAM and 29053/SRF/Cam, respectively) are deposited. URI: http://hdl.handle.net/10311/291 Files in this item: 1
Chemical constituents of Treculia.pdf (2.209Mb) -
Ngadjui, B.T.; Abegaz, B.M.; Keumedjio, F.; Folefoc, G.N.; Kapchec, G.W.F. (Elsevier Science Ltd. www.elsevier.com/locate/phytochem, NaN, 2002)[more][less]
Abstract: Three clerodane diterpenoids, crotozambefurans A, B and C were isolated from the stem bark of Croton zambesicus together with the known clerodane crotocorylifuran and two trachylobanes: 7b-acetoxytrachyloban-18-oic acid and trachyloban-7b, 18-diol. Betulinol, lupeol, sitosterol and its 3b-glucopyranosyl derivative were also obtained. The structures of crotozambefurans A, B and C were determined, respectively, as: 15,16-epoxy-1,3,13(16),14-clerodatetraen-20,12-olide-18,19-dioic acid dimethylester, 15,16-epoxy- 1,3,13(16),14-clerodatetraen-18,19,20-trioic acid trimethylester and 15,16-epoxy-3,13(16),14-clerodatrien-19,1a:20,12-diolide-18-oic acid methylester, using spectroscopic analysis, especially, NMR spectra in conjunction with 2D experiments, COSY, HSQC, HMBC and TOCSY. URI: http://hdl.handle.net/10311/251 Files in this item: 2
Diterpenoids from the stem bark.pdf (2.493Mb)license.txt (1.998Kb) -
Nindi, M.M.; Kgarebe, B.V.; Wolfender, J.L.; Abegaz, B.M. (John Wiley & Sons, Ltd., NaN, 1999)[more][less]
Abstract: Three naphthalenic derivatives, four flavonoids and two of the four anthraquinones previously isolated from the leaves of Rhamnus prinoides were successfully ionised under electrospray ionisation conditions. These compounds were subsequently detected in the leaf extract of the plant using electrospray liquid chromatography–mass spectrometry (LC–ESI–MS). The potential of LC–ESI–MS for screening a leaf extract, with the focus on the suitability of the method for assaying the bitter principle, geshoidin, of this commercially important plant, is presented. URI: http://hdl.handle.net/10311/290 Files in this item: 1
Electrospray Liquid.pdf (1.464Mb) -
Abegaz, B.M.; Bezabih, M.; Msuta, T.; Brun, R.; Menche, D.; Muhlbacher, J.; Bringmann, G. (American Chemical Society. http://pubs.acs.org/jnp/, NaN, 2002)[more][less]
Abstract: The novel phenylanthraquinones 4'-O-demethylknipholone-4'-O-β-D-glucopyranoside (2) and gaboroquinones A (3) and B (4) were isolated from the African medicinal plant Bulbine frutescens. Biaryl 2 represents the first phenylanthraquinone glucoside, while 3 and 4 are the first side-chain-hydroxylated phenylanthraquinones. Their constitutions were determined by spectroscopic analysis, in particular by HMBC, HMQC, and ROESY NMR investigations, and by chemical transformations. The axial configurations were elucidated chemically, by deglucosylation of 2 and by side-chain deoxygenation of 3 and 4 to give the known phenylanthraquinones 4'-O-demethylknipholone (5), isoknipholone (6), and knipholone (1), respectively, and chiroptically, by CD investigations. Compounds 2, 3, and 4 showed moderate to good antiplasmodial and antitrypanosomal activities in vitro. URI: http://hdl.handle.net/10311/346 Files in this item: 1
Gaboroquinones.pdf (407.3Kb) -
Ngamga, D.; Yankep, E.; Tane, P.; Bezabih, M.; Ngadjui, B.T.; Fomum, Z.T.; Abegaz, B.M. (Verlag der Zeitschrift fu¨r Naturforschung, Tu¨bingen · http://znaturforsch.com, NaN, 2005)[more][less]
Abstract: Three new isoflavonoids, griffonianone F, G and H were isolated from the seeds of Millettia griffoniana, along with the known prebarbigerone, pseudobaptigenin, pseudobaptigenin methyl ether, tephrosin, dipterixine, odorantine, 7,4’,5’-tetramethoxyisoflavone and isojamaicin. Their structures were assigned on the basis of spectroscopic data and chemical transformations. URI: http://hdl.handle.net/10311/274 Files in this item: 1
Isoflavonoids from Seeds.pdf (1.353Mb) -
Abegaz, B.M.; Ngadjui, B.T.; Bezabih, M.; Mdee, L.K. (International Union of Pure and Applied Chemistry. http://www.iupac.org/publications/pac/, NaN, 1999)[more][less]
Abstract: Marketed plants are an important but a vulnerable group of plants whose investigations as well as conservation should be considered with priority. The chemistry, and in some cases biological activities of novel iso¯avonoids, nor-lignans, anthracene and naphthalene derivatives and poly prenylated ¯avonoids isolated and characterized from Hagenia abyssinica, Salsola somalensis, Hypoxis spp., Taverniera abyssinica, Aloe spp., Bulbine capitata, Rhamnus prinoides and Dorstenia spp. are discussed. URI: http://hdl.handle.net/10311/289 Files in this item: 1
Novel natural products.pdf (4.533Mb) -
Kapche, G.D.W.F.; Fozing, C.D.; Donfack, J.H.; Fotso, G.W.; Amadou, D.; Tchana, A.N.; Bezabih, M.; Moundipa, P F; Ngadjui, B.N.; Abegaz, B.M. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2008)[more][less]
Abstract: Five prenylated arylbenzofurans, moracins Q–U, were isolated from Morus mesozygia (Moraceae). Their structures were elucidated on the basis of spectroscopic evidence. Along with these compounds, 3b-acetoxyurs- 12-en-11-one, marsformoxide, moracin C, moracin M, moracin K, artocarpesin, cycloartocarpesin, morachalcone A were also isolated. Four of the five compounds, (moracins R–U) displayed potent antioxidant activity. URI: http://hdl.handle.net/10311/315 Files in this item: 1
Prenylated arylbenzofuran.pdf (3.853Mb) -
Simo, I.K.; Ngadjui, B.T.; Abegaz, B.M. (Elsevier Ltd. www.elsevier.com/locate/biochemsyseco, June 18, 2005)[more][less]
Abstract: Dorstenia (Moraceae) is a mainly tropical genus of some 170 species (Mabberley, 1987). There are 23 species in Cameroon where a decoction of the leaves is administered for the treatment of cough, headache and stomach pain (Bouquet, 1969). The genus is made up largely of herbaceous perennials with succulent and non-succulent scrambling rhizomes (Berg et al., 1989). The twigs of Dorstenia angusticornis were collected in February 2002 from Kumba South West Province of Cameroon. Voucher specimen (No 28165/sfcam) is deposited at the National Herbarium Yaounde, Cameroon. URI: http://hdl.handle.net/10311/255 Files in this item: 1
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Abegaz, B.M.; Ngadjui, B.T.; Folefoc, G.N.; Fotso, S.; Ambassa, P.; Bezabih, M.; Dongo, E.; Rise, F.; Petersen, D. (Elsevier Ltd. www.elsevier.com/locate/phytochem, NaN, 2003)[more][less]
Abstract: A monoprenylated flavan and two monoterpenoid substituted furanocoumarins were isolated from the twigs of Dorstenia elliptica along with 3-(3,3-dimethylallyl)-4,20,40-trihydroxylchalcone, psoralen, bergapten, O-[3-(2,2-dimethyl-3-oxo-2H-furan-5-yl)butyl] bergaptol, b-sitosterol and its b-d-glucopyranoside. The structure of the flavan was determined as 6(1,1-dimethylallyl)-7,40- dihydroxylflavan and the monoterpenoid substituted furanocoumarins were assigned as O-[3-(2,2-dimethyl-3-oxo-2H-furan-5-yl)-3- hydroxybutyl]-bergaptol and O-[2-(5-hydroxy-2,6,6-trimethyl-3-oxo-2H-pyran-2-yl)ethyl]bergaptol, respectively, using spectroscopic analysis, especially, 2D NMR spectra. URI: http://hdl.handle.net/10311/286 Files in this item: 1
Prenylated flavonoids,.pdf (3.692Mb) -
Abegaz, B.M. (Chemical Society of Ethiopia. http://www.aau.edu.et/faculties/sc/CSE/home.html, NaN, 1996)[more][less]
URI: http://hdl.handle.net/10311/345 Files in this item: 1
progress in the chemistry of.pdf (922.3Kb) -
Majinda, R.R.T; Abegaz, B.M.; Bezabih, M.; Ngadjui, B.T; Wanjala, C.C.W.; Mdee, L.K.; Bojase, G.; Silayo, A.; Masesane, I.; Yeboah, S.O. (IUPAC. http://www.iupac.org/publications/pac/, NaN, 2001)[more][less]
Abstract: Marketed plants are very important items of trade in many parts of the world. The community uses these for a variety of purposes such as foods, cosmetics, flavors, spices, and medicines. It seems that plants that are used for medicinal purposes form the most common category. Four plants used for treatment of microbial infections, viz., Bolusanthus speciosus, Erythrina latissima, Crotalaria podocarpa, and Elephantorrhiza goetzei, were investigated, and these yielded several known and novel structures, some with appreciable antibiotic activity against the test organisms. The activity of some of the isolated plants and the parts of the plant from which these were obtained lend support to their traditional use. Bulbine abyssinica and B. capitata yielded phenylanthraquinones, some of which were shown to possess strong antiplasmodial activity. In addition, these yielded isofuranonaphthoquinones, which were also found to be weakly antiplasmodial and antioxidant. Scilla nervosa yielded several known and novel homoisoflavoinds of the 3-benzylchroman-4-ones and 3-benzylidinechroman- 4-one type, as well as some stilbenoids. The homoisoflavonoids showed strong antitumor activity against various cancer cell lines. Rhus pyroides gave a novel bichalcone, which showed weak antifeedant activity, consistent with the observation by farmers that the plant was avoided by corn cricket. Results from investigated Dorstenia species originating from Cameroon, Ethiopia, and Tanzania yielded styrenes, coumarins, chalcones, and flavonoids. The chalcones and flavonoids showed various levels of prenylation or geranylation, and an observation made so far is that prenylated flavonoids are only found in Dorstenia species of African origin. The only example of a bis-geranylated chalcone is found in Dorstenia. URI: http://hdl.handle.net/10311/308 Files in this item: 1
Recent results from.pdf (4.630Mb)
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