Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity

=olabellane diterpenes have considerable antiviral activityy but most studies have been focused towards compounds isolated from Dictyota brown algaeT %lthough soft corals are also a significant source of these diterpenesy their antiviral potential has not been studied in detailT With the aim of asse...

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Fecha de publicación:
2017
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
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Expeditio: repositorio UTadeo
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oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/9259
Acceso en línea:
https://doi.org/10.15446/rev.colomb.quim.v46n1.62830
http://hdl.handle.net/20.500.12010/9259
Palabra clave:
Soft coralsy
Eunicea
Dolabellane diterpenes
Antivirals
Corales -- Investigaciones
Química -- Investigaciones
Octocorales
Eunicea
Dolabellanos
Antivirales
Rights
License
Abierto (Texto Completo)
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repository_id_str
dc.title.spa.fl_str_mv Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
dc.title.alternative.eng.fl_str_mv Dolabellanos de los octocorales caribeños Eunicea laciniata y Eunicea asperula y determinación de su actividad anti VHS-1
title Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
spellingShingle Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
Soft coralsy
Eunicea
Dolabellane diterpenes
Antivirals
Corales -- Investigaciones
Química -- Investigaciones
Octocorales
Eunicea
Dolabellanos
Antivirales
title_short Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
title_full Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
title_fullStr Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
title_full_unstemmed Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
title_sort Dolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activity
dc.subject.spa.fl_str_mv Soft coralsy
Eunicea
Dolabellane diterpenes
Antivirals
topic Soft coralsy
Eunicea
Dolabellane diterpenes
Antivirals
Corales -- Investigaciones
Química -- Investigaciones
Octocorales
Eunicea
Dolabellanos
Antivirales
dc.subject.lemb.spa.fl_str_mv Corales -- Investigaciones
Química -- Investigaciones
dc.subject.keyword.spa.fl_str_mv Octocorales
Eunicea
Dolabellanos
Antivirales
description =olabellane diterpenes have considerable antiviral activityy but most studies have been focused towards compounds isolated from Dictyota brown algaeT %lthough soft corals are also a significant source of these diterpenesy their antiviral potential has not been studied in detailT With the aim of assessing the biological activity of marine sourcesy we evaluated the dolabellane content in the soft corals Eunicea laciniata and E. asperula collected in Santa Martay μolombian μaribbeanT =olabellanes 657 were isolated from E. laciniata while compounds Ky : and 0 were isolated from E. asperulaT %ll compounds were identified by NMRy éμA9OMSy optical rotation and comparison with previously reported dolabellanesT éμA9OMS analyses showed that dolabellatrienone JKz transforms into compounds : and 0 as oxidation products upon prolonged storage) howevery those compounds were also naturally present in the extract of the studied organismsT Pure dolabellanes were tested in vitro in antiviral assays against qSVA5T μompound 7 inhibited virus replication in infected cells JW:TWI of inhibition at f4 μMz without cytotoxic effect Jμμf4 ; EfEzy showing similar activity to the positive control %cyclovir®T Thusy compound 7 is an interesting candidate for further studies of dolabellanes as antiviralsT
publishDate 2017
dc.date.created.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2020-05-11T15:29:24Z
dc.date.available.none.fl_str_mv 2020-05-11T15:29:24Z
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.local.spa.fl_str_mv Artículo
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.identifier.issn.spa.fl_str_mv 2357-3791
dc.identifier.other.spa.fl_str_mv https://doi.org/10.15446/rev.colomb.quim.v46n1.62830
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/9259
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.15446/rev.colomb.quim.v46n1.62830
dc.identifier.instname.spa.fl_str_mv instname:Universidad de Bogotá Jorge Tadeo Lozano
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional de la Universidad de Bogotá Jorge Tadeo Lozano
identifier_str_mv 2357-3791
instname:Universidad de Bogotá Jorge Tadeo Lozano
reponame:Repositorio Institucional de la Universidad de Bogotá Jorge Tadeo Lozano
url https://doi.org/10.15446/rev.colomb.quim.v46n1.62830
http://hdl.handle.net/20.500.12010/9259
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.local.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.extent.spa.fl_str_mv 8 páginas
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.coverage.spatial.spa.fl_str_mv Bogotá, Colombia
dc.publisher.spa.fl_str_mv Universidad de Bogotá Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
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spelling Bogotá, Colombia2020-05-11T15:29:24Z2020-05-11T15:29:24Z20172357-3791https://doi.org/10.15446/rev.colomb.quim.v46n1.62830http://hdl.handle.net/20.500.12010/9259https://doi.org/10.15446/rev.colomb.quim.v46n1.62830instname:Universidad de Bogotá Jorge Tadeo Lozanoreponame:Repositorio Institucional de la Universidad de Bogotá Jorge Tadeo Lozano=olabellane diterpenes have considerable antiviral activityy but most studies have been focused towards compounds isolated from Dictyota brown algaeT %lthough soft corals are also a significant source of these diterpenesy their antiviral potential has not been studied in detailT With the aim of assessing the biological activity of marine sourcesy we evaluated the dolabellane content in the soft corals Eunicea laciniata and E. asperula collected in Santa Martay μolombian μaribbeanT =olabellanes 657 were isolated from E. laciniata while compounds Ky : and 0 were isolated from E. asperulaT %ll compounds were identified by NMRy éμA9OMSy optical rotation and comparison with previously reported dolabellanesT éμA9OMS analyses showed that dolabellatrienone JKz transforms into compounds : and 0 as oxidation products upon prolonged storage) howevery those compounds were also naturally present in the extract of the studied organismsT Pure dolabellanes were tested in vitro in antiviral assays against qSVA5T μompound 7 inhibited virus replication in infected cells JW:TWI of inhibition at f4 μMz without cytotoxic effect Jμμf4 ; EfEzy showing similar activity to the positive control %cyclovir®T Thusy compound 7 is an interesting candidate for further studies of dolabellanes as antiviralsT8os dolabellanos son diterpenos con actividad antiviraly la mayor parte de los estudios se han realizado con compuestos aislados de algas pardas del género DictyotaT 8os corales blandos son también una importante fuente de dolabellanosy pero el potencial antiviral de éstos ha sido muy poco estudiadoT Se llevó a cabo el estudio químico de los dolabellanos presentes en los octocorales Eunicea laciniata y Eunicea asperulay recolectados en Santa Martay μaribe colombianoT 8os dolabellanos 6A7 fueron aislados del octocoral E. laciniata mientras que en E. asperula se encontraron los compuestos Ky : y 0T 8a elucidación estructural se llevó a cabo mediante RMNy espectrometría de masasy rotación óptica y comparación con reportes previosT 9l análisis por μéA9M evidenció que la dolabellatrienona JKz se puede transformar en los compuestos : y 0 como producto del almacenamiento prolongadoy no obstantey tales compuestos también estuvieron presentes en los extractos de los organismos estudiadosT 9l compuesto 7 inhibió la replicación del VqSA5 JW:yWI de inhibición en células infectadas a una concentración de f4 μMz sin efecto citotóxico Jμμf4 ; EfEzy mostrando una citotoxicidad similar al %ciclovir®y un control positivoy por lo cual es un candidato para la realización de estudios adicionales sobre el potencial antiviral de los dolabellanosT8 páginasapplication/pdfUniversidad de Bogotá Jorge Tadeo LozanoSoft coralsyEuniceaDolabellane diterpenesAntiviralsCorales -- InvestigacionesQuímica -- InvestigacionesOctocoralesEuniceaDolabellanosAntiviralesDolabellane diterpenes from the Caribbean soft corals Eunicea laciniata and Eunicea asperula and determination of their anti HSV-1 activityDolabellanos de los octocorales caribeños Eunicea laciniata y Eunicea asperula y determinación de su actividad anti VHS-1Artículoinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Amaya García, FabiánSanchez Nuñez, Maria LeonisaRamos, Freddy APuyana, MónicaPalmer Paixão, Izabel Christina Nunes deLaneuville Teixeira, ValeriaCastellanos, LeonardoTHUMBNAIL9650.pdf.jpg9650.pdf.jpgIM Thumbnailimage/jpeg16415https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/9259/3/9650.pdf.jpg3dbf70043546609db2630d56d2e0b4bdMD53open accessORIGINAL9650.pdf9650.pdfVer artículoapplication/pdf1038074https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/9259/1/9650.pdfaa68b255170d33e1cabc0c530221b85aMD51open accessLICENSElicense.txtlicense.txttext/plain; charset=utf-82938https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/9259/2/license.txtabceeb1c943c50d3343516f9dbfc110fMD52open access20.500.12010/9259oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/92592020-05-11 10:32:57.959open accessRepositorio Institucional - Universidad Jorge Tadeo Lozanoexpeditio@utadeo.edu.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