Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"Extraction, standardization and assessment of the volatility of the sex attractants of Heterodera rostocheinsis Woll. and H. schachtii Schm"    Next AbstractGenome-wide association scan and phased haplotype construction for quantitative trait loci affecting boar taint in three pig breeds »

J Nat Prod


Title:"Mahorones, highly brominated cyclopentenones from the red alga Asparagopsis taxiformis"
Author(s):Greff S; Zubia M; Genta-Jouve G; Massi L; Perez T; Thomas OP;
Address:"Institut Mediterraneen de Biodiversite et d'Ecologie Marine et Continentale, IMBE UMR 7263 CNRS/IRD/ Aix-Marseille Universite/Universite d'Avignon et des Pays du Vaucluse , Station Marine d'Endoume, rue de la Batterie des Lions, 13007 Marseille, France"
Journal Title:J Nat Prod
Year:2014
Volume:20140418
Issue:5
Page Number:1150 - 1155
DOI: 10.1021/np401094h
ISSN/ISBN:1520-6025 (Electronic) 0163-3864 (Linking)
Abstract:"The red alga Asparagopsis taxiformis (Rhodophyta, Bonnemaisoniaceae) has been shown to produce a large diversity of halogenated volatile organic compounds, with one to four carbons. As the distribution of this alga may expand worldwide, we implemented a research program that aims to understand the functions of its specialized metabolome in marine ecosystems. Phytochemical investigations performed on A. taxiformis gametophyte stages from the Indian Ocean revealed two new highly brominated cyclopentenones named mahorone (1) and 5-bromomahorone (2). They are the first examples of natural 2,3-dibromocyclopentenone derivatives. Their structure elucidation was achieved using spectrometric methods including NMR and MS. A standardized ecotoxicological assay was used as an assessment of their role in the environment, revealing high toxicities for both compounds (EC50 0.16 muM for 1 and 2). Additionally, both compounds were evaluated in antibacterial, antifungal, and cytotoxicity assays. Compounds 1 and 2 exhibit mild antibacterial activities against the human pathogen Acinetobacter baumannii"
Keywords:Acinetobacter baumannii/drug effects Anti-Bacterial Agents/chemistry/*isolation & purification/*pharmacology Antifungal Agents/chemistry/*isolation & purification/*pharmacology Cyclopentanes/chemistry/*isolation & purification/*pharmacology Humans Hydroca;
Notes:"MedlineGreff, Stephane Zubia, Mayalen Genta-Jouve, Gregory Massi, Lionel Perez, Thierry Thomas, Olivier P eng Research Support, Non-U.S. Gov't 2014/04/22 J Nat Prod. 2014 May 23; 77(5):1150-5. doi: 10.1021/np401094h. Epub 2014 Apr 18"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 16-11-2024