Literature DB >> 12648540

Antibacterial bromophenols from the marine red alga Rhodomela confervoides.

Nianjun Xu1, Xiao Fan, Xiaojun Yan, Xiancui Li, Rongli Niu, C K Tseng.   

Abstract

Two bromophenols, together with three known compounds, were isolated from the methanolic extract of the marine alga, Rhodomela confervoides. By means of MS and NMR spectroscopic analyses, they were identified as 3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(hydroxymethyl) 1,2-benzenediol (1) and 3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5- (ethoxymethyl) 1,2-benzenediol (2). Three known compounds were also isolated, namely 3-bromo-4-[2,3-dibromo-4,5-dihydroxyphenyl] methyl-5-(methoxymethyl) 1,2-benzenediol (3), 4,4'- methylenebis [5,6-dibromo-1,2-benzenediol] (4) and bis (2,3-dibromo-4,5-dihydroxybenzyl) ether (5). Compound 5 was the most active against five strains of bacteria with the MIC less than 70 microg/ml, while compounds 2, 3 and 4 exhibited moderate activity.

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Year:  2003        PMID: 12648540     DOI: 10.1016/s0031-9422(03)00004-9

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  24 in total

Review 1.  Exploitation of marine algae: biogenic compounds for potential antifouling applications.

Authors:  Punyasloke Bhadury; Phillip C Wright
Journal:  Planta       Date:  2004-06-24       Impact factor: 4.116

Review 2.  Marine pharmacology in 2003-4: marine compounds with anthelmintic antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiplatelet, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of action.

Authors:  Alejandro M S Mayer; Abimael D Rodríguez; Roberto G S Berlinck; Mark T Hamann
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2007-02-09       Impact factor: 3.228

Review 3.  The major bioactive components of seaweeds and their mosquitocidal potential.

Authors:  Ke-Xin Yu; Ibrahim Jantan; Rohani Ahmad; Ching-Lee Wong
Journal:  Parasitol Res       Date:  2014-08-14       Impact factor: 2.289

4.  In vitro antiviral activity of red alga, Polysiphonia morrowii extract and its bromophenols against fish pathogenic infectious hematopoietic necrosis virus and infectious pancreatic necrosis virus.

Authors:  Su-Yeun Kim; Seok Ryel Kim; Myung-Joo Oh; Sung-Ju Jung; So Young Kang
Journal:  J Microbiol       Date:  2011-03-03       Impact factor: 3.422

5.  Biosynthesis of silver nanoparticles using Myristica fragrans seed (nutmeg) extract and its antibacterial activity against multidrug-resistant (MDR) Salmonella enterica serovar Typhi isolates.

Authors:  Senthilkumar Balakrishnan; Ilakkia Sivaji; Selvam Kandasamy; Senbagam Duraisamy; Nachimuthu Senthil Kumar; Guruswami Gurusubramanian
Journal:  Environ Sci Pollut Res Int       Date:  2017-05-03       Impact factor: 4.223

Review 6.  Bromophenols in marine algae and their bioactivities.

Authors:  Ming Liu; Poul Erik Hansen; Xiukun Lin
Journal:  Mar Drugs       Date:  2011-07-22       Impact factor: 6.085

Review 7.  Neuroprotective effects of marine algae.

Authors:  Ratih Pangestuti; Se-Kwon Kim
Journal:  Mar Drugs       Date:  2011-05-10       Impact factor: 6.085

Review 8.  Environmental Impact on Seaweed Phenolic Production and Activity: An Important Step for Compound Exploitation.

Authors:  Silvia Lomartire; João Cotas; Diana Pacheco; João Carlos Marques; Leonel Pereira; Ana M M Gonçalves
Journal:  Mar Drugs       Date:  2021-04-26       Impact factor: 5.118

9.  Structure based design of compounds from natural sources for diabetes and inflammation.

Authors:  Sivasubramanian Suhitha; Krishnaswamy Gunasekaran; Devadasan Velmurugan
Journal:  Bioinformation       Date:  2012-11-23

10.  Synthesis and α-glucosidase inhibitory mechanisms of bis(2,3-dibromo-4,5-dihydroxybenzyl) ether, a potential marine bromophenol α-glucosidase inhibitor.

Authors:  Ming Liu; Wei Zhang; Jianteng Wei; Xiukun Lin
Journal:  Mar Drugs       Date:  2011-09-19       Impact factor: 6.085

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