New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes

Detalhes bibliográficos
Autor(a) principal: Queiroz, Maria João R. P.
Data de Publicação: 2012
Outros Autores: Dias, Sofia, Peixoto, Daniela, Rodrigues, Ana Rita O., Oliveira, Andreia D. S., Coutinho, Paulo J. G., Silva, Luís A. Vale, Pinto, Eugénia, Castanheira, Elisabete M. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/19345
Resumo: New fluorescent methoxylated di(hetero)arylethers in the thieno[3,2-b]pyridine series were prepared by a copper-catalyzed Ullmann-type C-O coupling of the methyl 3-amino-6-bromothieno[3,2-b]pyridine-2-carboxylate with ortho, meta and para-methoxyphenols, using N,N-dimethylglycine as the ligand and Cs2CO3 as the base. The compounds obtained were tested for their inhibitory growth activity in three human tumor cell lines MCF-7 (breast adenocarcinoma), A375-C5 (melanoma), NCI-H460 (non-small cell lung cancer). The di(hetero)arylethers bearing a methoxy group in the ortho and meta positions showed very low GI50 values (1.1 - 2.5 µM) in all the three tumor cell lines. Their fluorescence properties in solution and when encapsulated in different nanoliposome formulations, composed either by egg-yolk phosphatidylcholine (Egg-PC), dipalmitoyl phosphatidylcholine (DPPC), dimyristoyl phosphatidylglycerol (DMPG), dioctadecyldimethylammonium bromide (DODAB), distearoyl phosphatidylcholine (DSPC), with or without cholesterol (Ch), or distearoyl phosphatidylethanolamine-(polyethylene glycol)2000 (DSPE-PEG), were studied. All compounds can be carried in the hydrophobic region of the liposome membrane. The liposomes with incorporated compounds are nanometric in size (diameter lower than 150 nm) and have generally low polydispersity.
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spelling New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomesUllmann-type C-O couplingDi(hetero)aryletersThieno[3,2-b]pyridinesFluorescenceNanoliposomesDi(hetero)arylethersThieno[3,2-blpyridinesScience & TechnologyNew fluorescent methoxylated di(hetero)arylethers in the thieno[3,2-b]pyridine series were prepared by a copper-catalyzed Ullmann-type C-O coupling of the methyl 3-amino-6-bromothieno[3,2-b]pyridine-2-carboxylate with ortho, meta and para-methoxyphenols, using N,N-dimethylglycine as the ligand and Cs2CO3 as the base. The compounds obtained were tested for their inhibitory growth activity in three human tumor cell lines MCF-7 (breast adenocarcinoma), A375-C5 (melanoma), NCI-H460 (non-small cell lung cancer). The di(hetero)arylethers bearing a methoxy group in the ortho and meta positions showed very low GI50 values (1.1 - 2.5 µM) in all the three tumor cell lines. Their fluorescence properties in solution and when encapsulated in different nanoliposome formulations, composed either by egg-yolk phosphatidylcholine (Egg-PC), dipalmitoyl phosphatidylcholine (DPPC), dimyristoyl phosphatidylglycerol (DMPG), dioctadecyldimethylammonium bromide (DODAB), distearoyl phosphatidylcholine (DSPC), with or without cholesterol (Ch), or distearoyl phosphatidylethanolamine-(polyethylene glycol)2000 (DSPE-PEG), were studied. All compounds can be carried in the hydrophobic region of the liposome membrane. The liposomes with incorporated compounds are nanometric in size (diameter lower than 150 nm) and have generally low polydispersity.Fundação para a Ciência e a Tecnologia (FCT) - Bruker Avance III 400-Univ. Minho).Fundo Europeu de Desenvolvimento Regional (FEDER)Research Centres, CQ/UM - PEstC/QUI/UI0686/2011, FCOMP-01-0124-FEDER-022716)] and CFUM [PEst-C/FIS/UI0607/2011, F-COMP-01-0124-FEDER-022711)], PTDC/QUI/81238/2006, (FCOMP-01-0124-FEDER-007467) (photophysical studies), PTDC/QUI-QUI/111060/2009 (F-COMP-01-0124-FEDER-015603) (organic synthesis and biological studies)COMPETE/QREN/EU.ElsevierUniversidade do MinhoQueiroz, Maria João R. P.Dias, SofiaPeixoto, DanielaRodrigues, Ana Rita O.Oliveira, Andreia D. S.Coutinho, Paulo J. G.Silva, Luís A. ValePinto, EugéniaCastanheira, Elisabete M. S.2012-062012-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/19345eng1010-603010.1016/j.jphotochem.2012.04.007www.sciencedirect.cominfo: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:RCAAP2023-07-21T12:21:39Zoai:repositorium.sdum.uminho.pt:1822/19345Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:14:58.529869Repositório 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 New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
title New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
spellingShingle New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
Queiroz, Maria João R. P.
Ullmann-type C-O coupling
Di(hetero)aryleters
Thieno[3,2-b]pyridines
Fluorescence
Nanoliposomes
Di(hetero)arylethers
Thieno[3,2-blpyridines
Science & Technology
title_short New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
title_full New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
title_fullStr New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
title_full_unstemmed New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
title_sort New potential antitumoral di(hetero)arylether derivatives in the thieno[3,2-b]pyridine series : synthesis and fluorescence studies in solution and in nanoliposomes
author Queiroz, Maria João R. P.
author_facet Queiroz, Maria João R. P.
Dias, Sofia
Peixoto, Daniela
Rodrigues, Ana Rita O.
Oliveira, Andreia D. S.
Coutinho, Paulo J. G.
Silva, Luís A. Vale
Pinto, Eugénia
Castanheira, Elisabete M. S.
author_role author
author2 Dias, Sofia
Peixoto, Daniela
Rodrigues, Ana Rita O.
Oliveira, Andreia D. S.
Coutinho, Paulo J. G.
Silva, Luís A. Vale
Pinto, Eugénia
Castanheira, Elisabete M. S.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Queiroz, Maria João R. P.
Dias, Sofia
Peixoto, Daniela
Rodrigues, Ana Rita O.
Oliveira, Andreia D. S.
Coutinho, Paulo J. G.
Silva, Luís A. Vale
Pinto, Eugénia
Castanheira, Elisabete M. S.
dc.subject.por.fl_str_mv Ullmann-type C-O coupling
Di(hetero)aryleters
Thieno[3,2-b]pyridines
Fluorescence
Nanoliposomes
Di(hetero)arylethers
Thieno[3,2-blpyridines
Science & Technology
topic Ullmann-type C-O coupling
Di(hetero)aryleters
Thieno[3,2-b]pyridines
Fluorescence
Nanoliposomes
Di(hetero)arylethers
Thieno[3,2-blpyridines
Science & Technology
description New fluorescent methoxylated di(hetero)arylethers in the thieno[3,2-b]pyridine series were prepared by a copper-catalyzed Ullmann-type C-O coupling of the methyl 3-amino-6-bromothieno[3,2-b]pyridine-2-carboxylate with ortho, meta and para-methoxyphenols, using N,N-dimethylglycine as the ligand and Cs2CO3 as the base. The compounds obtained were tested for their inhibitory growth activity in three human tumor cell lines MCF-7 (breast adenocarcinoma), A375-C5 (melanoma), NCI-H460 (non-small cell lung cancer). The di(hetero)arylethers bearing a methoxy group in the ortho and meta positions showed very low GI50 values (1.1 - 2.5 µM) in all the three tumor cell lines. Their fluorescence properties in solution and when encapsulated in different nanoliposome formulations, composed either by egg-yolk phosphatidylcholine (Egg-PC), dipalmitoyl phosphatidylcholine (DPPC), dimyristoyl phosphatidylglycerol (DMPG), dioctadecyldimethylammonium bromide (DODAB), distearoyl phosphatidylcholine (DSPC), with or without cholesterol (Ch), or distearoyl phosphatidylethanolamine-(polyethylene glycol)2000 (DSPE-PEG), were studied. All compounds can be carried in the hydrophobic region of the liposome membrane. The liposomes with incorporated compounds are nanometric in size (diameter lower than 150 nm) and have generally low polydispersity.
publishDate 2012
dc.date.none.fl_str_mv 2012-06
2012-06-01T00:00:00Z
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 https://hdl.handle.net/1822/19345
url https://hdl.handle.net/1822/19345
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1010-6030
10.1016/j.jphotochem.2012.04.007
www.sciencedirect.com
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eu_rights_str_mv openAccess
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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