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Synthesis of Cytotoxic Benzofurans and Ethers Derivatives of Paeonol.
Santo, Laura Patrícia Federal do Espírito; Costa de Almeida, Helori; Blandón Pardo, Jennifer Federal do Espírito; Santiago, Pedro; Ellena, Javier; Lacerda Júnior, Valdemar Federal do Espírito; Costa-Lotufo, Leticia Veras; Borges, Warley de Souza.
Afiliação
  • Santo LPFDE; Federal University of Espirito Santo, Department of Chemistry, Avenida Fernando Ferrari 514, Vitória, 29075910, Vitória, BRAZIL.
  • Costa de Almeida H; University of São Paulo, Department of Pharmacology, Cidade Universitária, São Paulo, 05508-900, São Paulo, BRAZIL.
  • Blandón Pardo JFDE; Federal University of Espirito Santo, Department of Chemistry, Avenida Fernando Ferrari 514, Vitória, 29075910, Vitória, BRAZIL.
  • Santiago P; University of Brasilia, Department of Physics, Campus Universitário Darcy Ribeiro, 70910-900, Brasília, BRAZIL.
  • Ellena J; USP São Carlos, Department of Physics, Av. Trabalhador são-carlense, 400, 13566-590, São Carlos, BRAZIL.
  • Lacerda Júnior VFDE; Federal University of Espirito Santo, Department of Chemistry, Avenida Fernando Ferrari 514, Vitória, 29075910, Vitória, BRAZIL.
  • Costa-Lotufo LV; University of São Paulo, Department of Pharmacology, Cidade Universitária, São Paulo, 05508-900, São Paulo, BRAZIL.
  • Borges WS; UFES: Universidade Federal do Espirito Santo, Química, Rua Dr. Moacyr Goncalves 129, Apto 403A, Vitória, 29060445, Vitória, BRAZIL.
Chem Biodivers ; : e202400943, 2024 Jul 16.
Article em En | MEDLINE | ID: mdl-39012301
ABSTRACT
Paeonol is a broadly studied natural product due to its many biological activities. Using a methodology previously employed by our research group, 11 derivatives of paeonol were synthesized (seven of them are unpublished compounds), including four ethers and seven benzofurans. Additionally, we determined the crystal structure of one of these ether derivatives (1a) and of five benzofuran derivatives (2a, 2b, 2c, 2f and 2g) by single crystal X-Ray diffraction. To continue studying the cytotoxicity of this natural product and its derivatives, all compounds were tested against two cancer cell lines, HCT116 and MCF-7. Compounds 2b, 2e, and 2g were considered active against the colorectal adenocarcinoma cells HCT116 (Growth inhibition > 60%). Compound 2e showed an IC50 of 0.2 µM and was selected for further analysis, results reinforce its anticancer potential.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article