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Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh
Two new chamigrane sesquiterpenes 1–2 and three known compounds 3–5 were isolated from a lipophilic extract of the red alga Laurencia dendroidea collected from the Southeastern Brazilian coast. Dendroidone (1) and dendroidiol (2) were isolated from samples collected at Biscaia Inlet, Angra dos Reis,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271906/ https://www.ncbi.nlm.nih.gov/pubmed/24642907 http://dx.doi.org/10.3390/molecules19033181 |
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author | Machado, Fernanda Lacerda da Silva Ventura, Thatiana Lopes Biá Gestinari, Lísia Mônica de Souza Cassano, Valéria Resende, Jackson Antônio Lamounier Camargos Kaiser, Carlos Roland Lasunskaia, Elena B. Muzitano, Michelle Frazão Soares, Angélica Ribeiro |
author_facet | Machado, Fernanda Lacerda da Silva Ventura, Thatiana Lopes Biá Gestinari, Lísia Mônica de Souza Cassano, Valéria Resende, Jackson Antônio Lamounier Camargos Kaiser, Carlos Roland Lasunskaia, Elena B. Muzitano, Michelle Frazão Soares, Angélica Ribeiro |
author_sort | Machado, Fernanda Lacerda da Silva |
collection | PubMed |
description | Two new chamigrane sesquiterpenes 1–2 and three known compounds 3–5 were isolated from a lipophilic extract of the red alga Laurencia dendroidea collected from the Southeastern Brazilian coast. Dendroidone (1) and dendroidiol (2) were isolated from samples collected at Biscaia Inlet, Angra dos Reis, Rio de Janeiro and at Manguinhos Beach, Serra, Espírito Santo, respectively. Debromoelatol (3), obtusane (4) and (1S*,2S*,3S*,5S*,8S*,9S*)-2,3,5,9-tetramethyltricyclo[6.3.0.01.5]undecan-2-ol (5) were obtained from specimens collected at Vermelha Beach, Parati, Rio de Janeiro. The structures of new compounds were elucidated by extensive NMR ((1)H-, (13)C-, COSY, HSQC, HMBC and NOESY) and high resolution mass spectrometry analysis. Additionally, the absolute configuration of compound 2 was assigned by X-ray analysis. Full spectroscopic data is described for the first time for compound 3. Anti-inflammatory and antimycobacterial activities of compounds 2–5 were evaluated. Compounds 3–5 inhibited the release of inflammatory mediator NO while TNF-α levels were only affected by 3. All compounds tested displayed moderate antimycobacterial action. |
format | Online Article Text |
id | pubmed-6271906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62719062018-12-20 Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh Machado, Fernanda Lacerda da Silva Ventura, Thatiana Lopes Biá Gestinari, Lísia Mônica de Souza Cassano, Valéria Resende, Jackson Antônio Lamounier Camargos Kaiser, Carlos Roland Lasunskaia, Elena B. Muzitano, Michelle Frazão Soares, Angélica Ribeiro Molecules Article Two new chamigrane sesquiterpenes 1–2 and three known compounds 3–5 were isolated from a lipophilic extract of the red alga Laurencia dendroidea collected from the Southeastern Brazilian coast. Dendroidone (1) and dendroidiol (2) were isolated from samples collected at Biscaia Inlet, Angra dos Reis, Rio de Janeiro and at Manguinhos Beach, Serra, Espírito Santo, respectively. Debromoelatol (3), obtusane (4) and (1S*,2S*,3S*,5S*,8S*,9S*)-2,3,5,9-tetramethyltricyclo[6.3.0.01.5]undecan-2-ol (5) were obtained from specimens collected at Vermelha Beach, Parati, Rio de Janeiro. The structures of new compounds were elucidated by extensive NMR ((1)H-, (13)C-, COSY, HSQC, HMBC and NOESY) and high resolution mass spectrometry analysis. Additionally, the absolute configuration of compound 2 was assigned by X-ray analysis. Full spectroscopic data is described for the first time for compound 3. Anti-inflammatory and antimycobacterial activities of compounds 2–5 were evaluated. Compounds 3–5 inhibited the release of inflammatory mediator NO while TNF-α levels were only affected by 3. All compounds tested displayed moderate antimycobacterial action. MDPI 2014-03-17 /pmc/articles/PMC6271906/ /pubmed/24642907 http://dx.doi.org/10.3390/molecules19033181 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Machado, Fernanda Lacerda da Silva Ventura, Thatiana Lopes Biá Gestinari, Lísia Mônica de Souza Cassano, Valéria Resende, Jackson Antônio Lamounier Camargos Kaiser, Carlos Roland Lasunskaia, Elena B. Muzitano, Michelle Frazão Soares, Angélica Ribeiro Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title | Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title_full | Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title_fullStr | Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title_full_unstemmed | Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title_short | Sesquiterpenes from the Brazilian Red Alga Laurencia dendroidea J. Agardh |
title_sort | sesquiterpenes from the brazilian red alga laurencia dendroidea j. agardh |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271906/ https://www.ncbi.nlm.nih.gov/pubmed/24642907 http://dx.doi.org/10.3390/molecules19033181 |
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