Published January 1, 2010
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New Nortriterpenoid and Ceramides From Stems and Leaves of Cultivated Triumfetta cordifolia A Rich (Tiliaceae)
Creators
- 1. Univ Yaounde I, Dept Organ Chem, Yaounde, Cameroon
- 2. Univ Yaounde I, Natl Adv Sch Engn, Yaounde, Cameroon
- 3. Univ Henri Poincare, Fac Sci, Lab Methodol RMN, Inst Jean Barriol, F-54506 Vandoeuvre Les Nancy, France
- 4. Univ Paul Verlaine Metz, Inst Jean Barriol, Lab Ingn Mol & Biochim Pharmaol, F-57070 Metz, France
- 5. Univ Versailles St Quentin en Yvelines, Inst Lavoisier Versailles, UMR 8086, F-78035 Versailles, France
Description
To highlight the role of plants in traditional healing, the leaves and the stems of cultivated Triumfetta cordifolia were phytochemically studied yielding a new nor-ursane type (1), a new ceramide (2) and a new piperidinic ceramide derivative (3) named, respectively, 2 alpha,19 alpha-dihydroxy-3-oxo-23-nor-urs-12-en-28-oic acid, (2R)-2-hydroxy-N-[(2S,3S,4R,26E)-1,3,4-trihydroxy-26-triaconten-2-yl] tetradecanamide and (2R,8Z)-2-hydroxy-{(2S,3R,5R,6S)-3,5-dihydroxy-6-[(1E,5Z)-hexadeca-1,5-dienyl]-2-(beta-d-glucopyranosyloxy)methyl piperidine-1-yl} tetracos-8-enamide (3). These were obtained together with lupeol (4), stigmasterol (5), 3-O-beta-d-glucopyranoside of beta-sitosterol (6), tormentic acid (7) from stems and heptadecanoic acid (8), beta-carotene (9), oleanolic acid (10), and 24-hydroxytormentic acid (11) from leaves. The structures were determined on the basis of NMR data (H-1-, C-13-, 2D-NMR analyses), mass spectrometry and confirmed by chemical transformations as well as comparison of spectral data with those reported in the literature. The FRAP method was used to evaluate the antioxidant activity of fractions collected from flash chromatography and isolated compounds. Among the fractions, four reduced Fe-III-TPTZ to Fe-II-TPTZ while isolated pure compounds showed no activity.
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