2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities

Autores
Mercader, Andrew Gustavo; Pomilio, Alicia Beatriz
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Flavonoids comprise a group of naturally occurring compounds that are known by their biological properties. Antiviral, antibacterial, antifungal, and antimycobacterial activities were analyzed. The results were discussed in terms of the bioactivity tested, and the structure-activity relationship (SAR), bidimensional (2D)- and three-dimensional (3D)- quantitative structure-activity relationship (QSAR) studies carried out on flavones, flavanones, chalcones, and some biflavonoids.
Fil: Mercader, Andrew Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
Fil: Pomilio, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
Materia
ANTIVIRAL, ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL AGENTS
BIFLAVONOIDS
CHALCONES
2D-QSAR
3D-QSAR
FLAVONES
FLAVANONES
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/268925

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network_name_str CONICET Digital (CONICET)
spelling 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activitiesMercader, Andrew GustavoPomilio, Alicia BeatrizANTIVIRAL, ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL AGENTSBIFLAVONOIDSCHALCONES2D-QSAR3D-QSARFLAVONESFLAVANONEShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Flavonoids comprise a group of naturally occurring compounds that are known by their biological properties. Antiviral, antibacterial, antifungal, and antimycobacterial activities were analyzed. The results were discussed in terms of the bioactivity tested, and the structure-activity relationship (SAR), bidimensional (2D)- and three-dimensional (3D)- quantitative structure-activity relationship (QSAR) studies carried out on flavones, flavanones, chalcones, and some biflavonoids.Fil: Mercader, Andrew Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; ArgentinaFil: Pomilio, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; ArgentinaBentham Science Publishers2012-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/268925Mercader, Andrew Gustavo; Pomilio, Alicia Beatriz; 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities; Bentham Science Publishers; Anti-Infective Agents; 10; 1; 1-2012; 41-542211-3525CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.benthamscience.com/article/40937info:eu-repo/semantics/altIdentifier/doi/10.2174/2211362611201010041info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:04:12Zoai:ri.conicet.gov.ar:11336/268925instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:04:12.458CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
title 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
spellingShingle 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
Mercader, Andrew Gustavo
ANTIVIRAL, ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL AGENTS
BIFLAVONOIDS
CHALCONES
2D-QSAR
3D-QSAR
FLAVONES
FLAVANONES
title_short 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
title_full 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
title_fullStr 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
title_full_unstemmed 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
title_sort 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities
dc.creator.none.fl_str_mv Mercader, Andrew Gustavo
Pomilio, Alicia Beatriz
author Mercader, Andrew Gustavo
author_facet Mercader, Andrew Gustavo
Pomilio, Alicia Beatriz
author_role author
author2 Pomilio, Alicia Beatriz
author2_role author
dc.subject.none.fl_str_mv ANTIVIRAL, ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL AGENTS
BIFLAVONOIDS
CHALCONES
2D-QSAR
3D-QSAR
FLAVONES
FLAVANONES
topic ANTIVIRAL, ANTIBACTERIAL, ANTIFUNGAL, ANTIMYCOBACTERIAL AGENTS
BIFLAVONOIDS
CHALCONES
2D-QSAR
3D-QSAR
FLAVONES
FLAVANONES
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Flavonoids comprise a group of naturally occurring compounds that are known by their biological properties. Antiviral, antibacterial, antifungal, and antimycobacterial activities were analyzed. The results were discussed in terms of the bioactivity tested, and the structure-activity relationship (SAR), bidimensional (2D)- and three-dimensional (3D)- quantitative structure-activity relationship (QSAR) studies carried out on flavones, flavanones, chalcones, and some biflavonoids.
Fil: Mercader, Andrew Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
Fil: Pomilio, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; Argentina
description Flavonoids comprise a group of naturally occurring compounds that are known by their biological properties. Antiviral, antibacterial, antifungal, and antimycobacterial activities were analyzed. The results were discussed in terms of the bioactivity tested, and the structure-activity relationship (SAR), bidimensional (2D)- and three-dimensional (3D)- quantitative structure-activity relationship (QSAR) studies carried out on flavones, flavanones, chalcones, and some biflavonoids.
publishDate 2012
dc.date.none.fl_str_mv 2012-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/268925
Mercader, Andrew Gustavo; Pomilio, Alicia Beatriz; 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities; Bentham Science Publishers; Anti-Infective Agents; 10; 1; 1-2012; 41-54
2211-3525
CONICET Digital
CONICET
url http://hdl.handle.net/11336/268925
identifier_str_mv Mercader, Andrew Gustavo; Pomilio, Alicia Beatriz; 2D- and 3D-QSAR studies of flavonoids, biflavones and chalcones: antiviral, antibacterial, antifungal, and antimycobacterial activities; Bentham Science Publishers; Anti-Infective Agents; 10; 1; 1-2012; 41-54
2211-3525
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.benthamscience.com/article/40937
info:eu-repo/semantics/altIdentifier/doi/10.2174/2211362611201010041
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Bentham Science Publishers
publisher.none.fl_str_mv Bentham Science Publishers
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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