Browsing by Author "Ngadjui, B.T."
Now showing items 1-10 of 10
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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.; 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) -
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) -
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) -
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)
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