File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Antifouling Activity of Secondary Metabolites Isolated from Chinese Marine Organisms

TitleAntifouling Activity of Secondary Metabolites Isolated from Chinese Marine Organisms
Authors
KeywordsAntilarval settlement
Marine natural products
Antifouling
Balanus amphitrite
Structure-activity relationship
Issue Date2013
Citation
Marine Biotechnology, 2013, v. 15, n. 5, p. 552-558 How to Cite?
AbstractBiofouling results in tremendous economic losses to maritime industries around the world. A recent global ban on the use of organotin compounds as antifouling agents has further raised demand for safe and effective antifouling compounds. In this study, 49 secondary metabolites, including diterpenoids, steroids, and polyketides, were isolated from soft corals, gorgonians, brown algae, and fungi collected along the coast of China, and their antifouling activity was tested against cyprids of the barnacle Balanus (Amphibalanus) amphitrite. Twenty of the compounds were found to inhibit larval settlement significantly at a concentration of 25 μg ml-1. Two briarane diterpenoids, juncin O (2) and juncenolide H (3), were the most promising non-toxic antilarval settlement candidates, with EC50 values less than 0.13 μg ml-1 and a safety ratio (LC50/EC50) higher than 400. A preliminary structure-activity relationships study indicated that both furanon and furan moieties are important for antifouling activity. Intriguingly, the presence of hydroxyls enhanced their antisettlement activity. © 2013 Springer Science+Business Media New York.
Persistent Identifierhttp://hdl.handle.net/10722/273655
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 0.553
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, Yong Xin-
dc.contributor.authorWu, Hui Xian-
dc.contributor.authorXu, Ying-
dc.contributor.authorShao, Chang Lun-
dc.contributor.authorWang, Chang Yun-
dc.contributor.authorQian, Pei Yuan-
dc.date.accessioned2019-08-12T09:56:16Z-
dc.date.available2019-08-12T09:56:16Z-
dc.date.issued2013-
dc.identifier.citationMarine Biotechnology, 2013, v. 15, n. 5, p. 552-558-
dc.identifier.issn1436-2228-
dc.identifier.urihttp://hdl.handle.net/10722/273655-
dc.description.abstractBiofouling results in tremendous economic losses to maritime industries around the world. A recent global ban on the use of organotin compounds as antifouling agents has further raised demand for safe and effective antifouling compounds. In this study, 49 secondary metabolites, including diterpenoids, steroids, and polyketides, were isolated from soft corals, gorgonians, brown algae, and fungi collected along the coast of China, and their antifouling activity was tested against cyprids of the barnacle Balanus (Amphibalanus) amphitrite. Twenty of the compounds were found to inhibit larval settlement significantly at a concentration of 25 μg ml-1. Two briarane diterpenoids, juncin O (2) and juncenolide H (3), were the most promising non-toxic antilarval settlement candidates, with EC50 values less than 0.13 μg ml-1 and a safety ratio (LC50/EC50) higher than 400. A preliminary structure-activity relationships study indicated that both furanon and furan moieties are important for antifouling activity. Intriguingly, the presence of hydroxyls enhanced their antisettlement activity. © 2013 Springer Science+Business Media New York.-
dc.languageeng-
dc.relation.ispartofMarine Biotechnology-
dc.subjectAntilarval settlement-
dc.subjectMarine natural products-
dc.subjectAntifouling-
dc.subjectBalanus amphitrite-
dc.subjectStructure-activity relationship-
dc.titleAntifouling Activity of Secondary Metabolites Isolated from Chinese Marine Organisms-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s10126-013-9502-7-
dc.identifier.scopuseid_2-s2.0-84881544291-
dc.identifier.volume15-
dc.identifier.issue5-
dc.identifier.spage552-
dc.identifier.epage558-
dc.identifier.isiWOS:000323107800005-
dc.identifier.issnl1436-2228-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats