Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity

Autores
Hergert, Lisandro Yamil; Nieto, Marcelo J.; Becerra, María Cecilia; Albesa, Inés; Mazzieri, Maria Rosa
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A series of benzenesulfonyl compounds, 1a-i, containing a BZT moiety was synthesized and characterized, and their antifungal and antibacterial activities were investigated. Compounds la and 1d showed the highest activity against Escherichia coli ATCC 25922; in addition la presented bactericidal activity against E. coli and Staphylococcus aureus at 8.6 mM. The ability of la to generate superoxide anion (O2-) was measured and it showed more stimuli in S. aureus compared to sulfafhiazole, indicating that 1a can be involved in oxidative stress of bacteria. None of the compounds inhibited the growth of the dermatophytes strains at the tested concentration (250 μg/ml). © 2008 Bentham Science Publishers Ltd.
Fil: Hergert, Lisandro Yamil. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
Fil: Nieto, Marcelo J.. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Southern Illinois University; Estados Unidos
Fil: Becerra, María Cecilia. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Fil: Albesa, Inés. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
Fil: Mazzieri, Maria Rosa. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
Materia
Antibacterial
Antifungal
Benzenesulfonyl
Benzotriazole
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:11336/64435
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/64435
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activityHergert, Lisandro YamilNieto, Marcelo J.Becerra, María CeciliaAlbesa, InésMazzieri, Maria RosaAntibacterialAntifungalBenzenesulfonylBenzotriazolehttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1A series of benzenesulfonyl compounds, 1a-i, containing a BZT moiety was synthesized and characterized, and their antifungal and antibacterial activities were investigated. Compounds la and 1d showed the highest activity against Escherichia coli ATCC 25922; in addition la presented bactericidal activity against E. coli and Staphylococcus aureus at 8.6 mM. The ability of la to generate superoxide anion (O2-) was measured and it showed more stimuli in S. aureus compared to sulfafhiazole, indicating that 1a can be involved in oxidative stress of bacteria. None of the compounds inhibited the growth of the dermatophytes strains at the tested concentration (250 μg/ml). © 2008 Bentham Science Publishers Ltd.Fil: Hergert, Lisandro Yamil. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; ArgentinaFil: Nieto, Marcelo J.. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Southern Illinois University; Estados UnidosFil: Becerra, María Cecilia. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Albesa, Inés. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; ArgentinaFil: Mazzieri, Maria Rosa. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; ArgentinaBentham Science Publishers2008-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/64435Hergert, Lisandro Yamil; Nieto, Marcelo J.; Becerra, María Cecilia; Albesa, Inés; Mazzieri, Maria Rosa; Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity; Bentham Science Publishers; Letters In Drug Design & Discovery; 5; 5; 7-2008; 313-3181570-18081875-628XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.eurekaselect.com/82876/articleinfo:eu-repo/semantics/altIdentifier/doi/10.2174/157018008784912108info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:39:43Zoai:ri.conicet.gov.ar:11336/64435instacron: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:34982025-09-29 10:39:43.792CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
title Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
spellingShingle Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
Hergert, Lisandro Yamil
Antibacterial
Antifungal
Benzenesulfonyl
Benzotriazole
title_short Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
title_full Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
title_fullStr Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
title_full_unstemmed Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
title_sort Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity
dc.creator.none.fl_str_mv Hergert, Lisandro Yamil
Nieto, Marcelo J.
Becerra, María Cecilia
Albesa, Inés
Mazzieri, Maria Rosa
author Hergert, Lisandro Yamil
author_facet Hergert, Lisandro Yamil
Nieto, Marcelo J.
Becerra, María Cecilia
Albesa, Inés
Mazzieri, Maria Rosa
author_role author
author2 Nieto, Marcelo J.
Becerra, María Cecilia
Albesa, Inés
Mazzieri, Maria Rosa
author2_role author
author
author
author
dc.subject.none.fl_str_mv Antibacterial
Antifungal
Benzenesulfonyl
Benzotriazole
topic Antibacterial
Antifungal
Benzenesulfonyl
Benzotriazole
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv A series of benzenesulfonyl compounds, 1a-i, containing a BZT moiety was synthesized and characterized, and their antifungal and antibacterial activities were investigated. Compounds la and 1d showed the highest activity against Escherichia coli ATCC 25922; in addition la presented bactericidal activity against E. coli and Staphylococcus aureus at 8.6 mM. The ability of la to generate superoxide anion (O2-) was measured and it showed more stimuli in S. aureus compared to sulfafhiazole, indicating that 1a can be involved in oxidative stress of bacteria. None of the compounds inhibited the growth of the dermatophytes strains at the tested concentration (250 μg/ml). © 2008 Bentham Science Publishers Ltd.
Fil: Hergert, Lisandro Yamil. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
Fil: Nieto, Marcelo J.. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Southern Illinois University; Estados Unidos
Fil: Becerra, María Cecilia. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Fil: Albesa, Inés. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
Fil: Mazzieri, Maria Rosa. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina
description A series of benzenesulfonyl compounds, 1a-i, containing a BZT moiety was synthesized and characterized, and their antifungal and antibacterial activities were investigated. Compounds la and 1d showed the highest activity against Escherichia coli ATCC 25922; in addition la presented bactericidal activity against E. coli and Staphylococcus aureus at 8.6 mM. The ability of la to generate superoxide anion (O2-) was measured and it showed more stimuli in S. aureus compared to sulfafhiazole, indicating that 1a can be involved in oxidative stress of bacteria. None of the compounds inhibited the growth of the dermatophytes strains at the tested concentration (250 μg/ml). © 2008 Bentham Science Publishers Ltd.
publishDate 2008
dc.date.none.fl_str_mv 2008-07
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/11336/64435
Hergert, Lisandro Yamil; Nieto, Marcelo J.; Becerra, María Cecilia; Albesa, Inés; Mazzieri, Maria Rosa; Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity; Bentham Science Publishers; Letters In Drug Design & Discovery; 5; 5; 7-2008; 313-318
1570-1808
1875-628X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/64435
identifier_str_mv Hergert, Lisandro Yamil; Nieto, Marcelo J.; Becerra, María Cecilia; Albesa, Inés; Mazzieri, Maria Rosa; Synthesis of N-benzenesulfonylbenzotriazole derivatives, and evaluation of their antimicrobial activity; Bentham Science Publishers; Letters In Drug Design & Discovery; 5; 5; 7-2008; 313-318
1570-1808
1875-628X
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.eurekaselect.com/82876/article
info:eu-repo/semantics/altIdentifier/doi/10.2174/157018008784912108
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
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
_version_ 1844614423168155648
score 13.070432

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