A new ergosterol analog, a new bis-anthraquinone and anti-obesity activity of anthraquinones from the marine sponge-associated fungus Talaromyces stipitatus KUFA 0207

Detalhes bibliográficos
Autor(a) principal: Noinart J.
Data de Publicação: 2017
Outros Autores: 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.
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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spelling 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
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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
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dc.format.none.fl_str_mv application/pdf
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instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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