2004
DOI: 10.1002/cbdv.200490039
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Extracts and Sesquiterpene Derivatives from the Red Alga Laurencia chondrioides with Antibacterial Activity against Fish and Human Pathogenic Bacteria

Abstract: During screening of seaweeds from different places in Europe for antimicrobial activities against human and fish pathogenic bacteria, Laurencia chondrioides was identified as a promising species. By bioassay-guided isolation, followed by structure elucidation by mass spectrometry and 1H- and 13C-NMR spectrometry, two sesquiterpenoides of the chamigrene-type from the selected red seaweed Laurencia chondrioides were identified. Both compounds inhibit the growth of some fish and human pathogenic bacteria.

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Cited by 36 publications
(28 citation statements)
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“…Among the Laurencia sesquiterpenes, elatol (59) can be singled out as the metabolite tested for its antimicrobial activity in the highest number of investigations, but the reported results are frequently contradictory, as even against the same strains variable levels of activity have been reported over the years [50,81,135,157,165,166,855,876,877].…”
Section: Antibacterial and Antifungal Activitymentioning
confidence: 99%
“…Among the Laurencia sesquiterpenes, elatol (59) can be singled out as the metabolite tested for its antimicrobial activity in the highest number of investigations, but the reported results are frequently contradictory, as even against the same strains variable levels of activity have been reported over the years [50,81,135,157,165,166,855,876,877].…”
Section: Antibacterial and Antifungal Activitymentioning
confidence: 99%
“…Halogenated secondary metabolites from red seaweed Laurencia chondrioides showed anti-bacterial activity against fish and human pathogenic bacteria [43]. There is also evidence that the red seaweed Delisea pulchra effectively avoids a broad spectrum of bacterial infections via its halogenated compounds known as furanones [44].…”
Section: Discussionmentioning
confidence: 99%
“…By enhancing the transcriptional activity of latent HIV-1 without inducing the polyclonal activation of non-infected cells, the viral reservoirs potentially could be purged of the virus. Thus, I3A (5) [155], IDB (57k) [156] and ingenol 3-hexanoate (ingenol-B) [154,157] showed outstanding reactivation properties, fully comparable to CD3/28 antibody stimulation, and, because of a lower toxicity profile when compared to other PKC modulators like bryostatin, all qualified as excellent latency-reversing agents. Thus, I3A (5) [155], IDB (57k) [156] and ingenol 3-hexanoate (ingenol-B) [154,157] showed outstanding reactivation properties, fully comparable to CD3/28 antibody stimulation, and, because of a lower toxicity profile when compared to other PKC modulators like bryostatin, all qualified as excellent latency-reversing agents.…”
Section: Antiviral Activitymentioning
confidence: 99%
“…Reversal of latency is related to the binding of NF-κB and related transcription factors to HIV-1 LTR (long terminal repeat) promoter, with triggering of viral RNA transcription [154]. A remarkable synergism was observed between ingenol-B and histone deacylase inhibitors like SAHA (suberoylanilidenehydroxamic acid), an effect not observed with IDB [157]. A remarkable synergism was observed between ingenol-B and histone deacylase inhibitors like SAHA (suberoylanilidenehydroxamic acid), an effect not observed with IDB [157].…”
Section: Antiviral Activitymentioning
confidence: 99%