Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues
Autor(a) principal: | |
---|---|
Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UnB |
Texto Completo: | http://repositorio.unb.br/handle/10482/30697 http://dx.doi.org/10.21577/0103-5053.20170075 |
Resumo: | Neolignans are a class of natural products with a wide range of biological effects. These substances are of great synthetic and biological interest, especially in searching for novel anticancer agents. In this paper, we report the synthesis of a new subclass of 8,4’-oxyneolignan analogues (β-ketoethers and β-ketoesters) and their cell viability assay on twenty four different cancer cells, among leukemias and carcinomas. Three compounds inhibited the growth of most human cancer cells. 2-Oxo-2-phenylethyl(2E)-3-[4-(2-oxo-2-phenylethoxy) phenyl]prop-2-enoate showed an antiproliferative activity superior to doxorubicin for U-87, U-138 MG and H1299 cell types and (E)-2-oxo-2-phenylethyl 3-(3-methoxy-4-(2-oxo-2-phenylethoxy)phenyl)acrylate was found to be very selective, demonstrating a growth inhibition of 92.0% against KG-1 cells. Furthermore, 1-oxo-1-phenylpropan-2-yl cinnamate exhibited significant inhibition activity in a range of 52.2 to 91.2% against twelve kinds of leukemia cell lines, revealing excellent results and very comparable to the reference drug. |
id |
UNB_7b7d5653a44cb89d26bc82e2deed3a2a |
---|---|
oai_identifier_str |
oai:repositorio.unb.br:10482/30697 |
network_acronym_str |
UNB |
network_name_str |
Repositório Institucional da UnB |
repository_id_str |
|
spelling |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analoguesCompostos orgânicosCâncer - tratamentoSínteseNeolignans are a class of natural products with a wide range of biological effects. These substances are of great synthetic and biological interest, especially in searching for novel anticancer agents. In this paper, we report the synthesis of a new subclass of 8,4’-oxyneolignan analogues (β-ketoethers and β-ketoesters) and their cell viability assay on twenty four different cancer cells, among leukemias and carcinomas. Three compounds inhibited the growth of most human cancer cells. 2-Oxo-2-phenylethyl(2E)-3-[4-(2-oxo-2-phenylethoxy) phenyl]prop-2-enoate showed an antiproliferative activity superior to doxorubicin for U-87, U-138 MG and H1299 cell types and (E)-2-oxo-2-phenylethyl 3-(3-methoxy-4-(2-oxo-2-phenylethoxy)phenyl)acrylate was found to be very selective, demonstrating a growth inhibition of 92.0% against KG-1 cells. Furthermore, 1-oxo-1-phenylpropan-2-yl cinnamate exhibited significant inhibition activity in a range of 52.2 to 91.2% against twelve kinds of leukemia cell lines, revealing excellent results and very comparable to the reference drug.Instituto de Química (IQ)Sociedade Brasileira de Química2018-01-04T19:14:43Z2018-01-04T19:14:43Z2017-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfSOUZA, Gisele C. et al. Synthesis, characterization and in vitro anticancer activity of Novel 8,4’-Oxyneolignan Analogues. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 11, p. 2229-2243, nov. 2017. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001102229&lng=en&nrm=iso>. Acesso em: 1 fev. 2018. doi: http://dx.doi.org/10.21577/0103-5053.20170075.http://repositorio.unb.br/handle/10482/30697http://dx.doi.org/10.21577/0103-5053.20170075Journal of the Brazilian Chemical Society - This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0). Fonte: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001102229&lng=en&nrm=iso. Acesso em: 1 fev. 2017.info:eu-repo/semantics/openAccessSouza, Gisele C.Franchi Jr., Gilberto C.Nowill, Alexandre E.Santos, Lourivaldo S.Alves, Cláudio N.Barata, Lauro E. S.Andrade, Carlos Kleber Zago deengreponame:Repositório Institucional da UnBinstname:Universidade de Brasília (UnB)instacron:UNB2023-10-20T14:01:19Zoai:repositorio.unb.br:10482/30697Repositório InstitucionalPUBhttps://repositorio.unb.br/oai/requestrepositorio@unb.bropendoar:2023-10-20T14:01:19Repositório Institucional da UnB - Universidade de Brasília (UnB)false |
dc.title.none.fl_str_mv |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
title |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
spellingShingle |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues Souza, Gisele C. Compostos orgânicos Câncer - tratamento Síntese |
title_short |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
title_full |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
title_fullStr |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
title_full_unstemmed |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
title_sort |
Synthesis, characterization and in vitro anticancer activity of Novel 8,4’ : oxyneolignan analogues |
author |
Souza, Gisele C. |
author_facet |
Souza, Gisele C. Franchi Jr., Gilberto C. Nowill, Alexandre E. Santos, Lourivaldo S. Alves, Cláudio N. Barata, Lauro E. S. Andrade, Carlos Kleber Zago de |
author_role |
author |
author2 |
Franchi Jr., Gilberto C. Nowill, Alexandre E. Santos, Lourivaldo S. Alves, Cláudio N. Barata, Lauro E. S. Andrade, Carlos Kleber Zago de |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Souza, Gisele C. Franchi Jr., Gilberto C. Nowill, Alexandre E. Santos, Lourivaldo S. Alves, Cláudio N. Barata, Lauro E. S. Andrade, Carlos Kleber Zago de |
dc.subject.por.fl_str_mv |
Compostos orgânicos Câncer - tratamento Síntese |
topic |
Compostos orgânicos Câncer - tratamento Síntese |
description |
Neolignans are a class of natural products with a wide range of biological effects. These substances are of great synthetic and biological interest, especially in searching for novel anticancer agents. In this paper, we report the synthesis of a new subclass of 8,4’-oxyneolignan analogues (β-ketoethers and β-ketoesters) and their cell viability assay on twenty four different cancer cells, among leukemias and carcinomas. Three compounds inhibited the growth of most human cancer cells. 2-Oxo-2-phenylethyl(2E)-3-[4-(2-oxo-2-phenylethoxy) phenyl]prop-2-enoate showed an antiproliferative activity superior to doxorubicin for U-87, U-138 MG and H1299 cell types and (E)-2-oxo-2-phenylethyl 3-(3-methoxy-4-(2-oxo-2-phenylethoxy)phenyl)acrylate was found to be very selective, demonstrating a growth inhibition of 92.0% against KG-1 cells. Furthermore, 1-oxo-1-phenylpropan-2-yl cinnamate exhibited significant inhibition activity in a range of 52.2 to 91.2% against twelve kinds of leukemia cell lines, revealing excellent results and very comparable to the reference drug. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-11 2018-01-04T19:14:43Z 2018-01-04T19:14:43Z |
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 |
SOUZA, Gisele C. et al. Synthesis, characterization and in vitro anticancer activity of Novel 8,4’-Oxyneolignan Analogues. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 11, p. 2229-2243, nov. 2017. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001102229&lng=en&nrm=iso>. Acesso em: 1 fev. 2018. doi: http://dx.doi.org/10.21577/0103-5053.20170075. http://repositorio.unb.br/handle/10482/30697 http://dx.doi.org/10.21577/0103-5053.20170075 |
identifier_str_mv |
SOUZA, Gisele C. et al. Synthesis, characterization and in vitro anticancer activity of Novel 8,4’-Oxyneolignan Analogues. Journal of the Brazilian Chemical Society, São Paulo, v. 28, n. 11, p. 2229-2243, nov. 2017. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001102229&lng=en&nrm=iso>. Acesso em: 1 fev. 2018. doi: http://dx.doi.org/10.21577/0103-5053.20170075. |
url |
http://repositorio.unb.br/handle/10482/30697 http://dx.doi.org/10.21577/0103-5053.20170075 |
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.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UnB instname:Universidade de Brasília (UnB) instacron:UNB |
instname_str |
Universidade de Brasília (UnB) |
instacron_str |
UNB |
institution |
UNB |
reponame_str |
Repositório Institucional da UnB |
collection |
Repositório Institucional da UnB |
repository.name.fl_str_mv |
Repositório Institucional da UnB - Universidade de Brasília (UnB) |
repository.mail.fl_str_mv |
repositorio@unb.br |
_version_ |
1810580706610380800 |