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A new ursane-type triterpene oxoglucopyranoside from Crossopteryx febrifuga.
Kayangar, Modjinan; Ngansop Nono, Raymond; Kühlborn, Jonas; Tchuenguem, Roland; Ponou, Beaudelaire K; Jenett-Siems, Kristina; Teponno, Rémy B; Dzoyem, Jean P; Opatz, Till; Melzig, Matthias F; Tapondjou, Léon A.
Affiliation
  • Kayangar M; Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Ngansop Nono R; Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Kühlborn J; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, D-55128 Mainz, Germany.
  • Tchuenguem R; Department of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Ponou BK; Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Jenett-Siems K; Institut für Pharmazie (Pharmazeutische Biologie), Freie Universität Berlin, Königin-Luise-Str. 2-4, D-14195 Berlin, Germany.
  • Teponno RB; Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Dzoyem JP; Department of Biochemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon.
  • Opatz T; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, D-55128 Mainz, Germany.
  • Melzig MF; Institut für Pharmazie (Pharmazeutische Biologie), Freie Universität Berlin, Königin-Luise-Str. 2-4, D-14195 Berlin, Germany.
  • Tapondjou LA; Department of Chemistry, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon, Phone: +237-675004826.
Z Naturforsch C J Biosci ; 74(11-12): 289-293, 2019 Nov 26.
Article in En | MEDLINE | ID: mdl-31525160
ABSTRACT
A new saponin, 3-O-ß-d-3-oxo-glucopyranosyl-ursa-12,20(30)-diene-27,28-dioic acid (1), was isolated from the methanol extract of stem bark of Crossopteryx febrifuga together with the known 3ß-d-glucopyranosyl-ursa-12,20(30)-diene-27,28-dioic acid (2), shanzhiside methyl ester (3), shanzhiside (4), ß-sitosterol (5), ß-sitosterol-3-O-ß-d-glucopyranoside (6), ursa-12,20(30)-diene-27,28-dioic acid (7), hederagenin (8), and oleanolic acid (9). The structures were established by comprehensive interpretation of their spectral data 1D- (1H and 13C), 2D-NMR (1H-1H COSY, HMQC, HMBC), spectroscopic, and electrospray ionisation time-of-flight mass spectrometry analysis. The isolated compounds and extracts were screened for their antibacterial properties. Although the EtOAc and n-BuOH extracts exhibited considerable antibacterial activity against Pseudomonas aeruginosa with minimum inhibitory concentration (MIC) value of 32 µg/mL, compounds 2 and 8 showed moderate activity against Enterococcus faecalis with MIC values of 256 and 128 µg/mL, respectively. The new compound (1) exhibited a moderate antibacterial activity against Staphylococcus aureus with an MIC value of 512 µg/mL.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Triterpenes / Rubiaceae / Glucosides Language: En Journal: Z Naturforsch C J Biosci Year: 2019 Document type: Article Affiliation country: Cameroon

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Triterpenes / Rubiaceae / Glucosides Language: En Journal: Z Naturforsch C J Biosci Year: 2019 Document type: Article Affiliation country: Cameroon