• Keine Ergebnisse gefunden

Flavonoid Glycosides and their p-Coumaroyl Esters from Campylospermum calanthum Leaves

N/A
N/A
Protected

Academic year: 2022

Aktie "Flavonoid Glycosides and their p-Coumaroyl Esters from Campylospermum calanthum Leaves"

Copied!
1
0
0

Wird geladen.... (Jetzt Volltext ansehen)

Volltext

(1)

Flavonoid Glycosides and their p-Coumaroyl Esters from Campylospermum calanthum Leaves

Savio S. Elo Mangaa, Anastasie E. Tiha, Bintou Abderamaneb, Raphael T. Ghogomua,*, Alain Blondc, and Bernard Bodoc

a Faculty of Science, Department of Organic Chemistry, University of Yaounde 1, P. O. Box 812, Yaounde, Cameroon. E-mail: ghogomut@uy1.uninet.cm

b Faculté des Sciences, Université de Ndjamena, P. O. Box 127, Ndjamena, Tchad

c Laboratoire de Chimie des Substances Naturelles, Muséum National d’Histoire Naturelle, 63 Rue Buffon, 75005 Paris, France

* Author for correspondence and reprint requests

Z. Naturforsch. 67 c, 233 – 243 (2012); received August 19, 2011/January 20, 2012

Six new compounds, comprising three fl avonoid glycosides and their respective coumaroyl esters, have been isolated and characterized from the methanol extract of the leaves of Campylospermum calanthum, along with three known fl avonoid aglycones, 7-O-methyl api- genin (1), 7-O-methyl luteolin (2), and 7-O-methyl quercetin (3). Their structures were elu- cidated based on chemical evidence as well as spectroscopic analysis including 1D and 2D NMR (1H-1H COSY, HSQC, HMBC, and NOESY) spectroscopy and by comparing their spectral data with those reported for related compounds.

Key words: Campylospermum calanthum, Ochnaceae, Flavonoid Glycosides, Coumaroyl Esters

Referenzen

ÄHNLICHE DOKUMENTE

Their chemical structures were determined on the basis of 1D- and 2D-NMR spectra (HSQC, HMBC) of their peracetylated derivatives, MALDI- TOF-mass spectra, and

e Present address: Near East University, Faculty of Pharmacy, Department of Pharmacognosy and Pharmaceutical Botany, Nicosia, Turkish Republic of Northern Cyprus. Reprint requests

Their structures were determined by means of 1D and 2D NMR spectroscopy, including 1 H- 1 H COSY, NOESY, HSQC and HMBC experiments, which resulted in complete

a Chemistry of Natural Products Group, Nobel Project, National Research Centre (NRC), El-BehoosSt., Dokki, Cairo, EgyptZ. Fax: +20 23 37

Ð Under UV-light, it appeared as pink-purple spot, turned to light green colour with FeCl 3 , and showed a weak and unclear change with ammonia vapours and naturstoff spray reagent

Their structures were elucidated by spectroscopic methods, including one- and two-dimensional NMR (COSY, HMQC, HMBC and ROESY). Key words: Parepigynum funingense,

From the leaves of Zizyphus glabrata, a new dammarane-type triterpene, pseudojujubogenin -3-O- β -D-glucopyranoside, along with the known ceanothane triterpenes, granulosic

two Gaussian functions for the P 1 and P 3 peaks and a Lorentzian function for the P 2 peak, revealing the ex- istence of three types of protons in the structure (Ta- ble 4). The