A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Texto Completo: | https://hdl.handle.net/10216/120500 |
Resumo: | A new ergosterol analog, talarosterone (1) and a new bis-anthraquinone derivative (3) were isolated, together with ten known compounds including palmitic acid, ergosta-4,6,8(14),22- tetraen-3-one, ergosterol-5,8-endoperoxide, cyathisterone (2), emodin (4a), questinol (4b), citreorosein (4c), fallacinol (4d), rheoemodin (4e) and secalonic acid A (5), from the ethyl acetate extract of the culture of the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207. The structures of the new compounds were established based on extensive 1D and 2D spectral analysis, and in the case of talarosterone (1), the absolute configurations of its stereogenic carbons were determined by X-ray crystallographic analysis. The structure and stereochemistry of cyathisterone (2) was also confirmed by X-ray analysis. The anthraquinones 4a-e and secalonic acid A (5) were tested for their anti-obesity activity using the zebrafish Nile red assay. Only citreorosein (4c) and questinol (4b) exhibited significant anti-obesity activity, while emodin (4a) and secalonic acid A (5) caused toxicity (death) for all exposed zebrafish larvae after 24 h. © 2017 by the authors. Licensee MDPI. |
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A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207anthraquinone derivativecitreoroseincyathisteroneemodinergosta 4,6,8(14),22 tetraen 3 oneergosterol 5,8 endoperoxidefallacinolpalmitic acidquestinolresveratrolrheoemodinsecalonic acid Asterol derivativetalarosteroneunclassified drugadultanimal experimentArticlecontrolled studycrystal structuredrug structureembryononhumanobesitysponge (Porifera)stereochemistryStylissa flabelliformisTalaromycesTalaromyces stipitatusX ray crystallographyzebra fishA new ergosterol analog, talarosterone (1) and a new bis-anthraquinone derivative (3) were isolated, together with ten known compounds including palmitic acid, ergosta-4,6,8(14),22- tetraen-3-one, ergosterol-5,8-endoperoxide, cyathisterone (2), emodin (4a), questinol (4b), citreorosein (4c), fallacinol (4d), rheoemodin (4e) and secalonic acid A (5), from the ethyl acetate extract of the culture of the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207. The structures of the new compounds were established based on extensive 1D and 2D spectral analysis, and in the case of talarosterone (1), the absolute configurations of its stereogenic carbons were determined by X-ray crystallographic analysis. The structure and stereochemistry of cyathisterone (2) was also confirmed by X-ray analysis. The anthraquinones 4a-e and secalonic acid A (5) were tested for their anti-obesity activity using the zebrafish Nile red assay. Only citreorosein (4c) and questinol (4b) exhibited significant anti-obesity activity, while emodin (4a) and secalonic acid A (5) caused toxicity (death) for all exposed zebrafish larvae after 24 h. © 2017 by the authors. Licensee MDPI.MDPI20172017-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/120500eng1660339710.3390/md15050139Noinart J.Buttachon S.Dethoup T.Gales L.Pereira J.A.Urbatzka R.Freitas S.Lee M.Silva A.M.S.Pinto M.M.M.Vasconcelos V.Kijjoa A.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-27T17:46:20Zoai:repositorio-aberto.up.pt:10216/120500Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T22:26:12.840440Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
title |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
spellingShingle |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 Noinart J. anthraquinone derivative citreorosein cyathisterone emodin ergosta 4,6,8(14),22 tetraen 3 one ergosterol 5,8 endoperoxide fallacinol palmitic acid questinol resveratrol rheoemodin secalonic acid A sterol derivative talarosterone unclassified drug adult animal experiment Article controlled study crystal structure drug structure embryo nonhuman obesity sponge (Porifera) stereochemistry Stylissa flabelliformis Talaromyces Talaromyces stipitatus X ray crystallography zebra fish |
title_short |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
title_full |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
title_fullStr |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
title_full_unstemmed |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
title_sort |
A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207 |
author |
Noinart J. |
author_facet |
Noinart J. Buttachon S. Dethoup T. Gales L. Pereira J.A. Urbatzka R. Freitas S. Lee M. Silva A.M.S. Pinto M.M.M. Vasconcelos V. Kijjoa A. |
author_role |
author |
author2 |
Buttachon S. Dethoup T. Gales L. Pereira J.A. Urbatzka R. Freitas S. Lee M. Silva A.M.S. Pinto M.M.M. Vasconcelos V. Kijjoa A. |
author2_role |
author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Noinart J. Buttachon S. Dethoup T. Gales L. Pereira J.A. Urbatzka R. Freitas S. Lee M. Silva A.M.S. Pinto M.M.M. Vasconcelos V. Kijjoa A. |
dc.subject.por.fl_str_mv |
anthraquinone derivative citreorosein cyathisterone emodin ergosta 4,6,8(14),22 tetraen 3 one ergosterol 5,8 endoperoxide fallacinol palmitic acid questinol resveratrol rheoemodin secalonic acid A sterol derivative talarosterone unclassified drug adult animal experiment Article controlled study crystal structure drug structure embryo nonhuman obesity sponge (Porifera) stereochemistry Stylissa flabelliformis Talaromyces Talaromyces stipitatus X ray crystallography zebra fish |
topic |
anthraquinone derivative citreorosein cyathisterone emodin ergosta 4,6,8(14),22 tetraen 3 one ergosterol 5,8 endoperoxide fallacinol palmitic acid questinol resveratrol rheoemodin secalonic acid A sterol derivative talarosterone unclassified drug adult animal experiment Article controlled study crystal structure drug structure embryo nonhuman obesity sponge (Porifera) stereochemistry Stylissa flabelliformis Talaromyces Talaromyces stipitatus X ray crystallography zebra fish |
description |
A new ergosterol analog, talarosterone (1) and a new bis-anthraquinone derivative (3) were isolated, together with ten known compounds including palmitic acid, ergosta-4,6,8(14),22- tetraen-3-one, ergosterol-5,8-endoperoxide, cyathisterone (2), emodin (4a), questinol (4b), citreorosein (4c), fallacinol (4d), rheoemodin (4e) and secalonic acid A (5), from the ethyl acetate extract of the culture of the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207. The structures of the new compounds were established based on extensive 1D and 2D spectral analysis, and in the case of talarosterone (1), the absolute configurations of its stereogenic carbons were determined by X-ray crystallographic analysis. The structure and stereochemistry of cyathisterone (2) was also confirmed by X-ray analysis. The anthraquinones 4a-e and secalonic acid A (5) were tested for their anti-obesity activity using the zebrafish Nile red assay. Only citreorosein (4c) and questinol (4b) exhibited significant anti-obesity activity, while emodin (4a) and secalonic acid A (5) caused toxicity (death) for all exposed zebrafish larvae after 24 h. © 2017 by the authors. Licensee MDPI. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2017-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10216/120500 |
url |
https://hdl.handle.net/10216/120500 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
16603397 10.3390/md15050139 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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