Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids

Detalhes bibliográficos
Autor(a) principal: Teixeira, José
Data de Publicação: 2013
Outros Autores: Silva, Tiago, Benfeito, Sofia, Gaspar, Alexandra, Garrido, E. Manuela, Garrido, Jorge, Borges, Fernanda
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/3529
Resumo: Phenolic acids are ubiquitous antioxidants accounting for approximately one third of the phenolic compounds in our diet. Their importance was supported by epidemiological studies that suggest an inverse relationship between dietary intake of phenolic antioxidants and the occurrence of diseases, such as cancer and neurodegenerative disorders. However, until now, most of natural antioxidants have limited therapeutic success a fact that could be related with their limited distribution throughout the body and with the inherent difficulties to attain the target sites. The development of phenolic antioxidants based on a hybrid concept and structurally based on natural hydroxybenzoic (gallic acid) and hydroxycinnamic (caffeic acid) scaffolds seems to be a suitable solution to surpass the mentioned drawbacks. Galloylecinnamic hybrids were synthesized and their antioxidant activity as well as partition coefficients and redox potentials evaluated. The structureepropertyeactivity relationship (SPAR) study revealed the existence of a correlation between the redox potentials and antioxidant activity. The galloylecinnamic acid hybrid stands out as the best antioxidant supplementing the effect of a blend of gallic acid plus caffeic acid endorsing the hypothesis that the whole is greater than the sum of the parts. In addition, some hybrid compounds possess an appropriate lipophilicity allowing their application as chain-breaking antioxidant in biomembranes or other type of lipidic systems. Their predicted ADME properties are also in accordance with the general requirements for drug-like compounds. Accordingly, these phenolic hybrids can be seen as potential antioxidants for tackling the oxidative status linked to the neurodegenerative, inflammatory or cancer processes.
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spelling Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybridsCinnamic acidGallic acidHybrid antioxidantsAntioxidant activityRedox potentialSPARDrug-like propertiesPhenolic acids are ubiquitous antioxidants accounting for approximately one third of the phenolic compounds in our diet. Their importance was supported by epidemiological studies that suggest an inverse relationship between dietary intake of phenolic antioxidants and the occurrence of diseases, such as cancer and neurodegenerative disorders. However, until now, most of natural antioxidants have limited therapeutic success a fact that could be related with their limited distribution throughout the body and with the inherent difficulties to attain the target sites. The development of phenolic antioxidants based on a hybrid concept and structurally based on natural hydroxybenzoic (gallic acid) and hydroxycinnamic (caffeic acid) scaffolds seems to be a suitable solution to surpass the mentioned drawbacks. Galloylecinnamic hybrids were synthesized and their antioxidant activity as well as partition coefficients and redox potentials evaluated. The structureepropertyeactivity relationship (SPAR) study revealed the existence of a correlation between the redox potentials and antioxidant activity. The galloylecinnamic acid hybrid stands out as the best antioxidant supplementing the effect of a blend of gallic acid plus caffeic acid endorsing the hypothesis that the whole is greater than the sum of the parts. In addition, some hybrid compounds possess an appropriate lipophilicity allowing their application as chain-breaking antioxidant in biomembranes or other type of lipidic systems. Their predicted ADME properties are also in accordance with the general requirements for drug-like compounds. Accordingly, these phenolic hybrids can be seen as potential antioxidants for tackling the oxidative status linked to the neurodegenerative, inflammatory or cancer processes.ElsevierRepositório Científico do Instituto Politécnico do PortoTeixeira, JoséSilva, TiagoBenfeito, SofiaGaspar, AlexandraGarrido, E. ManuelaGarrido, JorgeBorges, Fernanda2014-01-30T15:05:37Z20132013-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/3529eng0223-523410.1016/j.ejmech.2012.12.049info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T12:43:17Zoai:recipp.ipp.pt:10400.22/3529Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:24:27.716483Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
title Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
spellingShingle Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
Teixeira, José
Cinnamic acid
Gallic acid
Hybrid antioxidants
Antioxidant activity
Redox potential
SPAR
Drug-like properties
title_short Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
title_full Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
title_fullStr Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
title_full_unstemmed Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
title_sort Exploring nature profits: development of novel and potent lipophilic antioxidants based on galloylecinnamic hybrids
author Teixeira, José
author_facet Teixeira, José
Silva, Tiago
Benfeito, Sofia
Gaspar, Alexandra
Garrido, E. Manuela
Garrido, Jorge
Borges, Fernanda
author_role author
author2 Silva, Tiago
Benfeito, Sofia
Gaspar, Alexandra
Garrido, E. Manuela
Garrido, Jorge
Borges, Fernanda
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Teixeira, José
Silva, Tiago
Benfeito, Sofia
Gaspar, Alexandra
Garrido, E. Manuela
Garrido, Jorge
Borges, Fernanda
dc.subject.por.fl_str_mv Cinnamic acid
Gallic acid
Hybrid antioxidants
Antioxidant activity
Redox potential
SPAR
Drug-like properties
topic Cinnamic acid
Gallic acid
Hybrid antioxidants
Antioxidant activity
Redox potential
SPAR
Drug-like properties
description Phenolic acids are ubiquitous antioxidants accounting for approximately one third of the phenolic compounds in our diet. Their importance was supported by epidemiological studies that suggest an inverse relationship between dietary intake of phenolic antioxidants and the occurrence of diseases, such as cancer and neurodegenerative disorders. However, until now, most of natural antioxidants have limited therapeutic success a fact that could be related with their limited distribution throughout the body and with the inherent difficulties to attain the target sites. The development of phenolic antioxidants based on a hybrid concept and structurally based on natural hydroxybenzoic (gallic acid) and hydroxycinnamic (caffeic acid) scaffolds seems to be a suitable solution to surpass the mentioned drawbacks. Galloylecinnamic hybrids were synthesized and their antioxidant activity as well as partition coefficients and redox potentials evaluated. The structureepropertyeactivity relationship (SPAR) study revealed the existence of a correlation between the redox potentials and antioxidant activity. The galloylecinnamic acid hybrid stands out as the best antioxidant supplementing the effect of a blend of gallic acid plus caffeic acid endorsing the hypothesis that the whole is greater than the sum of the parts. In addition, some hybrid compounds possess an appropriate lipophilicity allowing their application as chain-breaking antioxidant in biomembranes or other type of lipidic systems. Their predicted ADME properties are also in accordance with the general requirements for drug-like compounds. Accordingly, these phenolic hybrids can be seen as potential antioxidants for tackling the oxidative status linked to the neurodegenerative, inflammatory or cancer processes.
publishDate 2013
dc.date.none.fl_str_mv 2013
2013-01-01T00:00:00Z
2014-01-30T15:05:37Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.22/3529
url http://hdl.handle.net/10400.22/3529
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0223-5234
10.1016/j.ejmech.2012.12.049
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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