aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives
Autor(a) principal: | |
---|---|
Data de Publicação: | 2013 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFLA |
Texto Completo: | http://www.sciencedirect.com/science/article/pii/S0167701213002005 http://repositorio.ufla.br/jspui/handle/1/4719 |
Resumo: | The antibacterial activity against Bacillus subtilis, Staphylococcus aureus and Escherichia coli, as well as the an- tifungal activity against Aspergillus niger of a series of anilide derivatives have been modeled using augment- ed multivariate image analysis applied to quantitative structure–activity relationship (aug-MIA-QSAR). This QSAR approach is based on 2D molecular shape, as well as atomic sizes and colors to encode chemical, phys- ical and biological properties. Predictive models with r 2 from 0.65 to 0.83 were used to estimate the antimi- crobial activities of novel anilide analogs, which were built from the combination of substructures of the most active antimicrobial compounds along the series. Given the synergistic effect of different substituents to pro- vide new molecules, promising compounds were proposed, highlighting a considerable multi-antimicrobial activity. |
id |
UFLA_ccfa259ba0656e07058475fadbe6d6c7 |
---|---|
oai_identifier_str |
oai:localhost:1/4719 |
network_acronym_str |
UFLA |
network_name_str |
Repositório Institucional da UFLA |
repository_id_str |
|
spelling |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivativesAnilide derivativesAntibacterial activityAntifungal activityChemometricsThe antibacterial activity against Bacillus subtilis, Staphylococcus aureus and Escherichia coli, as well as the an- tifungal activity against Aspergillus niger of a series of anilide derivatives have been modeled using augment- ed multivariate image analysis applied to quantitative structure–activity relationship (aug-MIA-QSAR). This QSAR approach is based on 2D molecular shape, as well as atomic sizes and colors to encode chemical, phys- ical and biological properties. Predictive models with r 2 from 0.65 to 0.83 were used to estimate the antimi- crobial activities of novel anilide analogs, which were built from the combination of substructures of the most active antimicrobial compounds along the series. Given the synergistic effect of different substituents to pro- vide new molecules, promising compounds were proposed, highlighting a considerable multi-antimicrobial activity.2014-12-02T20:18:39Z2014-12-02T20:18:39Z2013-06-26info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleNUNES, C. A.; FREITAS, M. P. aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives. Journal of Microbiological Methods, Amsterdam, v. 94, n. 3, p. 217-220, Sept. 2013.http://www.sciencedirect.com/science/article/pii/S0167701213002005http://repositorio.ufla.br/jspui/handle/1/4719Journal of Microbiological Methodsreponame:Repositório Institucional da UFLAinstname:Universidade Federal de Lavras (UFLA)instacron:UFLANunes, C. A.Freitas, M. P.info:eu-repo/semantics/openAccesseng2014-12-04T10:50:50Zoai:localhost:1/4719Repositório InstitucionalPUBhttp://repositorio.ufla.br/oai/requestnivaldo@ufla.br || repositorio.biblioteca@ufla.bropendoar:2014-12-04T10:50:50Repositório Institucional da UFLA - Universidade Federal de Lavras (UFLA)false |
dc.title.none.fl_str_mv |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
title |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
spellingShingle |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives Nunes, C. A. Anilide derivatives Antibacterial activity Antifungal activity Chemometrics |
title_short |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
title_full |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
title_fullStr |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
title_full_unstemmed |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
title_sort |
aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives |
author |
Nunes, C. A. |
author_facet |
Nunes, C. A. Freitas, M. P. |
author_role |
author |
author2 |
Freitas, M. P. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Nunes, C. A. Freitas, M. P. |
dc.subject.por.fl_str_mv |
Anilide derivatives Antibacterial activity Antifungal activity Chemometrics |
topic |
Anilide derivatives Antibacterial activity Antifungal activity Chemometrics |
description |
The antibacterial activity against Bacillus subtilis, Staphylococcus aureus and Escherichia coli, as well as the an- tifungal activity against Aspergillus niger of a series of anilide derivatives have been modeled using augment- ed multivariate image analysis applied to quantitative structure–activity relationship (aug-MIA-QSAR). This QSAR approach is based on 2D molecular shape, as well as atomic sizes and colors to encode chemical, phys- ical and biological properties. Predictive models with r 2 from 0.65 to 0.83 were used to estimate the antimi- crobial activities of novel anilide analogs, which were built from the combination of substructures of the most active antimicrobial compounds along the series. Given the synergistic effect of different substituents to pro- vide new molecules, promising compounds were proposed, highlighting a considerable multi-antimicrobial activity. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06-26 2014-12-02T20:18:39Z 2014-12-02T20:18:39Z |
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 |
NUNES, C. A.; FREITAS, M. P. aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives. Journal of Microbiological Methods, Amsterdam, v. 94, n. 3, p. 217-220, Sept. 2013. http://www.sciencedirect.com/science/article/pii/S0167701213002005 http://repositorio.ufla.br/jspui/handle/1/4719 |
identifier_str_mv |
NUNES, C. A.; FREITAS, M. P. aug-MIA-QSAR modeling of antimicrobial activities and design of multi-target anilide derivatives. Journal of Microbiological Methods, Amsterdam, v. 94, n. 3, p. 217-220, Sept. 2013. |
url |
http://www.sciencedirect.com/science/article/pii/S0167701213002005 http://repositorio.ufla.br/jspui/handle/1/4719 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Journal of Microbiological Methods reponame:Repositório Institucional da UFLA instname:Universidade Federal de Lavras (UFLA) instacron:UFLA |
instname_str |
Universidade Federal de Lavras (UFLA) |
instacron_str |
UFLA |
institution |
UFLA |
reponame_str |
Repositório Institucional da UFLA |
collection |
Repositório Institucional da UFLA |
repository.name.fl_str_mv |
Repositório Institucional da UFLA - Universidade Federal de Lavras (UFLA) |
repository.mail.fl_str_mv |
nivaldo@ufla.br || repositorio.biblioteca@ufla.br |
_version_ |
1815439353446400000 |