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Melantheraside A–E, five original triterpenes with natural chloride or oxime group from the aerial parts of Melanthera elliptica O. Hoffm

Authors :
David Ngnokam
Laurence Voutquenne-Nazabadioko
Cyrille Ngoufack Tagousop
Dominique Harakat
Université de Dschang
Institut de Chimie Moléculaire de Reims - UMR 7312 (ICMR)
SFR Condorcet
Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-SFR CAP Santé (Champagne-Ardenne Picardie Santé)
Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Source :
Phytochemistry Letters, Phytochemistry Letters, Elsevier, 2018, 26, pp.38-43. ⟨10.1016/j.phytol.2018.05.007⟩
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

International audience; Five new pentacyclic triterpenoids, Melantheraside A–E (1–5) together with eleven known compounds (6-16) were isolated from the methanol extract of the aerial parts of Melanthera elliptica O. Hoffm. Their structures were established by extensive analysis of 1D- (1H, 13C), 2D- (COSY, ROESY, HSQC and HMBC) NMR data experiments in conjunction with mass spectrometry (TOFESIMS and HR-TOFESIMS) and by comparison with data reported in the literature. The structures of the new compounds were established as: 12α-chloro-3β-hydroxyoleanan-28,13β-olide (1), 3β-acetoxy-12α-hydroxytaraxer-14-en-28-oic acid (2), 3β-hydroxy-12-oximetaraxeran-28,14β-olide (3), 3β-acetoxy-12-oximetaraxeran-28,14β-olide (4) and 2β-carboxyamino-12α-chloro-3-oxo-1-nor-oleanan-28,13β-olide (5). The 3β-acetoxy-12α-chloro-oleanan-28,13β-olide (6) was isolated for the first time as natural product.

Details

ISSN :
18743900
Volume :
26
Database :
OpenAIRE
Journal :
Phytochemistry Letters
Accession number :
edsair.doi.dedup.....23a014abe901945f0e947ef70b563532