Aurantoside C, a New Tetramic Acid Glycoside from the Sponge Homophymia conferta

A new tetramic acid glycoside, aurantoside C (3), was isolated from the sponge Homophymia conferta and the structure was determined by detailed 1D and 2D NMR analysis of the natural product and a hexaacetate derivative.

Saved in:
Bibliographic Details
Published in:Journal of natural products (Washington, D.C.) D.C.), 1999-01, Vol.62 (1), p.170-172
Main Authors: Wolf, Dietmar, Schmitz, Francis J, Qiu, Feng, Kelly-Borges, Michelle
Format: Article
Language:English
Subjects:
AGENTES ANTINEOPLASTICOS
Analytical, structural and metabolic biochemistry
Animals
ANTINEOPLASTIC AGENTS
Aromatic and heterocyclic compounds
Biological and medical sciences
CHEMICAL COMPOSITION
CHEMICAL STRUCTURE
COMPOSICION QUIMICA
COMPOSITION CHIMIQUE
CYTOTOXIC COMPOUNDS
ESPECTROMETRIA
ESTRUCTURA QUIMICA
FILIPINAS
Fundamental and applied biological sciences. Psychology
GLICOSIDOS
GLYCOSIDE
GLYCOSIDES
Glycosides - chemistry
Glycosides - isolation & purification
Glycosides - pharmacology
Heterocyclic compounds, pigments
Homophymia conferta
Magnetic Resonance Spectroscopy
MEDICAMENT CYTOSTATIQUE
METABOLITE
METABOLITES
METABOLITOS
Molecular Structure
Other biological molecules
PARAZOA
PHARMACEUTICAL PRODUCTS
PHILIPPINES
Porifera - chemistry
Pyrrolidinones - chemistry
Pyrrolidinones - isolation & purification
Pyrrolidinones - pharmacology
SPECTRAL ANALYSIS
SPECTROMETRIE
SPECTROMETRY
Spectrum Analysis
STRUCTURE CHIMIQUE
SUBSTANCE TOXIQUE
SUSTANCIAS TOXICAS
TOXIC SUBSTANCES
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A new tetramic acid glycoside, aurantoside C (3), was isolated from the sponge Homophymia conferta and the structure was determined by detailed 1D and 2D NMR analysis of the natural product and a hexaacetate derivative.
ISSN:0163-3864
1520-6025
DOI:10.1021/np980283x