TY - JOUR
T1 - New flavonoids from the underground parts of Eriosema laurentii
AU - Ateba, Sylvin Benjamin
AU - Njamen, Dieudonne
AU - Ukowitz, Katrin
AU - Zehl, Martin
AU - Kählig, Hanspeter
AU - Hobiger, Stefanie
AU - Jungbauer, Alois
AU - Krenn, Liselotte
N1 - Publisher Copyright:
© 2016 Phytochemical Society of Europe
PY - 2016/12
Y1 - 2016/12
N2 - Pharmacological, toxicological and phytochemical investigations of aerial parts of Eriosema laurentii De Wild. (Leguminosae), a plant used in traditional African medicine, showed a complex pattern of very rare and several new exceptional phenolic compounds. In continuation of the phytochemical work and based on the activity of an extract from the underground parts, the presented study showed the occurrence of a new pyranoisoflavone, named methyleriosemaone D, and a new highly prenylated (2S,3S)-6,8,3'-triprenyl-3,5,7,2',4'-pentahydroxyflavanone in these parts of E. laurentii. In addition, the very rare pyranoisoflavone eriosemaone D was proven in this plant for the first time. All structures were elucidated unambiguously by extensive MS- and one and two-dimensional NMR-experiments. Detailed NMR spectra of eriosemaone D were included to rationalize the correction of some of the previously reported carbon signals in the
13C NMR spectrum. The estrogenic activity of the extract and isolated compounds was tested in an estrogen receptor α yeast transactivation assay.
AB - Pharmacological, toxicological and phytochemical investigations of aerial parts of Eriosema laurentii De Wild. (Leguminosae), a plant used in traditional African medicine, showed a complex pattern of very rare and several new exceptional phenolic compounds. In continuation of the phytochemical work and based on the activity of an extract from the underground parts, the presented study showed the occurrence of a new pyranoisoflavone, named methyleriosemaone D, and a new highly prenylated (2S,3S)-6,8,3'-triprenyl-3,5,7,2',4'-pentahydroxyflavanone in these parts of E. laurentii. In addition, the very rare pyranoisoflavone eriosemaone D was proven in this plant for the first time. All structures were elucidated unambiguously by extensive MS- and one and two-dimensional NMR-experiments. Detailed NMR spectra of eriosemaone D were included to rationalize the correction of some of the previously reported carbon signals in the
13C NMR spectrum. The estrogenic activity of the extract and isolated compounds was tested in an estrogen receptor α yeast transactivation assay.
KW - Eriosema laurentii De Wild
KW - Leguminosae
KW - Eriosemaone D
KW - Methyleriosemaone D
KW - (2S,3S)-6,8,3 '-Triprenyl-3,5,7,2 ',4 '-pentahydroxyflavanone
KW - IONIZATION MASS-SPECTROMETRY
KW - LIQUID-CHROMATOGRAPHY
KW - PRENYLATED FLAVONOIDS
KW - ANTHELMINTIC ACTIVITY
KW - RICH SOURCE
KW - CONSTITUENTS
KW - LEGUMINOSAE
KW - DIVOIRE
KW - EXTRACT
KW - WILD
KW - (2S,3S)-6,8,3'-Triprenyl-3,5,7,2',4'-pentahydroxyflavanone
UR - https://www.scopus.com/pages/publications/84991650683
U2 - 10.1016/j.phytol.2016.10.003
DO - 10.1016/j.phytol.2016.10.003
M3 - Article
SN - 1874-3900
VL - 18
SP - 144
EP - 149
JO - Phytochemistry Letters
JF - Phytochemistry Letters
ER -