Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine

Detalhes bibliográficos
Autor(a) principal: Almeida, Vitor Y. G.
Data de Publicação: 2020
Outros Autores: Rocha, Josias S., Felix, Débora P., Oliveira, Gabriela P., Lima, Mauro A., Farias, Renan L. [UNESP], Zanetti, Renan D. [UNESP], Netto, Adelino V. G. [UNESP], Zambom, Carolina R. [UNESP], Garrido, Saulo S. [UNESP], Rocha, Fillipe V.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/slct.202004093
http://hdl.handle.net/11449/206948
Resumo: The present work aimed to evaluate the biological activities of the silver (I) complexes, with the formulae [Ag(L)(PPh3)2]+ and [Ag(L)2]+ (L=(E)-2-((E)-3-phenylallylidene) hydrazine-1-carboxamide – CSC and (2E)-2-[(3E)-4-phenylbut-3-en-2-ylidene]-hydrazinecarboxamide – BSC). Four new silver(I) compounds were synthesized and characterized by NMR 1H, 13C-{1H}, 31P, IR, and UV-Vis spectroscopies, molar conductivity, and elemental analysis (CNH). High cytotoxicity was found for all complexes being more active than cisplatin in the tested cell lines. The antibacterial assay demonstrated that the compounds without phosphine groups presented high levels of inhibition (80 %) at 70.4 uM against the Gram-positive and Gram-negative bacteria strains. The DNA interactions were investigated by UV-Vis DNA titration, electrophoresis, and circular dichroism experiments. Data showed that the compounds did not interact with DNA in the tested conditions. However, the compounds have provided important information about the structural features that are needed in order to design new silver (I) complexes with biological activities.
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spelling Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and TriphenylphosphineAntibacterialAntiproliferationDNA interactionNMR spectroscopySilver (I)The present work aimed to evaluate the biological activities of the silver (I) complexes, with the formulae [Ag(L)(PPh3)2]+ and [Ag(L)2]+ (L=(E)-2-((E)-3-phenylallylidene) hydrazine-1-carboxamide – CSC and (2E)-2-[(3E)-4-phenylbut-3-en-2-ylidene]-hydrazinecarboxamide – BSC). Four new silver(I) compounds were synthesized and characterized by NMR 1H, 13C-{1H}, 31P, IR, and UV-Vis spectroscopies, molar conductivity, and elemental analysis (CNH). High cytotoxicity was found for all complexes being more active than cisplatin in the tested cell lines. The antibacterial assay demonstrated that the compounds without phosphine groups presented high levels of inhibition (80 %) at 70.4 uM against the Gram-positive and Gram-negative bacteria strains. The DNA interactions were investigated by UV-Vis DNA titration, electrophoresis, and circular dichroism experiments. Data showed that the compounds did not interact with DNA in the tested conditions. However, the compounds have provided important information about the structural features that are needed in order to design new silver (I) complexes with biological activities.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Chemistry Department Federal University of São Carlos Rod. Washington Luis Km 235Department of Analytical Chemistry Physicochemical and Inorganic Chemistry. UNESP – Univ Estadual Paulista Institute of Chemistry Av. Prof. Francisco Degni 55Department of Biochemistry and Organic Chemistry. UNESP – Univ Estadual Paulista Institute of Chemistry Av. Prof. Francisco Degni 55Department of Analytical Chemistry Physicochemical and Inorganic Chemistry. UNESP – Univ Estadual Paulista Institute of Chemistry Av. Prof. Francisco Degni 55Department of Biochemistry and Organic Chemistry. UNESP – Univ Estadual Paulista Institute of Chemistry Av. Prof. Francisco Degni 55FAPESP: 2018/03018-1FAPESP: 2019/17584-1FAPESP: FAPESP 2019/11242-1Km 235Universidade Estadual Paulista (Unesp)Almeida, Vitor Y. G.Rocha, Josias S.Felix, Débora P.Oliveira, Gabriela P.Lima, Mauro A.Farias, Renan L. [UNESP]Zanetti, Renan D. [UNESP]Netto, Adelino V. G. [UNESP]Zambom, Carolina R. [UNESP]Garrido, Saulo S. [UNESP]Rocha, Fillipe V.2021-06-25T10:46:33Z2021-06-25T10:46:33Z2020-12-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article14559-14563http://dx.doi.org/10.1002/slct.202004093ChemistrySelect, v. 5, n. 46, p. 14559-14563, 2020.2365-6549http://hdl.handle.net/11449/20694810.1002/slct.2020040932-s2.0-85097440819Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengChemistrySelectinfo:eu-repo/semantics/openAccess2021-10-23T15:48:27Zoai:repositorio.unesp.br:11449/206948Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T15:48:27Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
title Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
spellingShingle Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
Almeida, Vitor Y. G.
Antibacterial
Antiproliferation
DNA interaction
NMR spectroscopy
Silver (I)
title_short Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
title_full Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
title_fullStr Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
title_full_unstemmed Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
title_sort Cytotoxicity and Antibacterial Activity of Silver Complexes Bearing Semicarbazones and Triphenylphosphine
author Almeida, Vitor Y. G.
author_facet Almeida, Vitor Y. G.
Rocha, Josias S.
Felix, Débora P.
Oliveira, Gabriela P.
Lima, Mauro A.
Farias, Renan L. [UNESP]
Zanetti, Renan D. [UNESP]
Netto, Adelino V. G. [UNESP]
Zambom, Carolina R. [UNESP]
Garrido, Saulo S. [UNESP]
Rocha, Fillipe V.
author_role author
author2 Rocha, Josias S.
Felix, Débora P.
Oliveira, Gabriela P.
Lima, Mauro A.
Farias, Renan L. [UNESP]
Zanetti, Renan D. [UNESP]
Netto, Adelino V. G. [UNESP]
Zambom, Carolina R. [UNESP]
Garrido, Saulo S. [UNESP]
Rocha, Fillipe V.
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Km 235
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Almeida, Vitor Y. G.
Rocha, Josias S.
Felix, Débora P.
Oliveira, Gabriela P.
Lima, Mauro A.
Farias, Renan L. [UNESP]
Zanetti, Renan D. [UNESP]
Netto, Adelino V. G. [UNESP]
Zambom, Carolina R. [UNESP]
Garrido, Saulo S. [UNESP]
Rocha, Fillipe V.
dc.subject.por.fl_str_mv Antibacterial
Antiproliferation
DNA interaction
NMR spectroscopy
Silver (I)
topic Antibacterial
Antiproliferation
DNA interaction
NMR spectroscopy
Silver (I)
description The present work aimed to evaluate the biological activities of the silver (I) complexes, with the formulae [Ag(L)(PPh3)2]+ and [Ag(L)2]+ (L=(E)-2-((E)-3-phenylallylidene) hydrazine-1-carboxamide – CSC and (2E)-2-[(3E)-4-phenylbut-3-en-2-ylidene]-hydrazinecarboxamide – BSC). Four new silver(I) compounds were synthesized and characterized by NMR 1H, 13C-{1H}, 31P, IR, and UV-Vis spectroscopies, molar conductivity, and elemental analysis (CNH). High cytotoxicity was found for all complexes being more active than cisplatin in the tested cell lines. The antibacterial assay demonstrated that the compounds without phosphine groups presented high levels of inhibition (80 %) at 70.4 uM against the Gram-positive and Gram-negative bacteria strains. The DNA interactions were investigated by UV-Vis DNA titration, electrophoresis, and circular dichroism experiments. Data showed that the compounds did not interact with DNA in the tested conditions. However, the compounds have provided important information about the structural features that are needed in order to design new silver (I) complexes with biological activities.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-11
2021-06-25T10:46:33Z
2021-06-25T10:46:33Z
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 http://dx.doi.org/10.1002/slct.202004093
ChemistrySelect, v. 5, n. 46, p. 14559-14563, 2020.
2365-6549
http://hdl.handle.net/11449/206948
10.1002/slct.202004093
2-s2.0-85097440819
url http://dx.doi.org/10.1002/slct.202004093
http://hdl.handle.net/11449/206948
identifier_str_mv ChemistrySelect, v. 5, n. 46, p. 14559-14563, 2020.
2365-6549
10.1002/slct.202004093
2-s2.0-85097440819
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv ChemistrySelect
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 14559-14563
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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