Your browser doesn't support javascript.
loading
Synthesis, structural characterization and biological activity of novel Knoevenagel condensates on DLD-1 human colon carcinoma.
Risianová, Lucia; Fischer-Fodor, Eva; Valentová, Jindra; Tatomir, Corina; Corina Decea, Nicoleta; Virag, Piroska; Pechová, Iveta; Devínsky, Ferdinand; Miklásová, Natalia.
Afiliação
  • Risianová L; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University in Bratislava, Kaliniciakova 8, Bratislava 83232, Slovakia.
  • Fischer-Fodor E; Institute of Oncology "I. Chiricuta", Cluj-Napoca 400015, Romania; Medfuture Research Center, University of Medicine and Pharmacy "Iuliu Hatieganu" Cluj Napoca, 400012 Cluj-Napoca, Romania.
  • Valentová J; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University in Bratislava, Kaliniciakova 8, Bratislava 83232, Slovakia.
  • Tatomir C; Institute of Oncology "I. Chiricuta", Cluj-Napoca 400015, Romania.
  • Corina Decea N; Department of Physiology, University of Medicine and Pharmacy "Iuliu Hatieganu" Cluj Napoca, 400012 Cluj-Napoca, Romania.
  • Virag P; Institute of Oncology "I. Chiricuta", Cluj-Napoca 400015, Romania.
  • Pechová I; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University in Bratislava, Kaliniciakova 8, Bratislava 83232, Slovakia.
  • Devínsky F; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University in Bratislava, Kaliniciakova 8, Bratislava 83232, Slovakia.
  • Miklásová N; Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University in Bratislava, Kaliniciakova 8, Bratislava 83232, Slovakia. Electronic address: miklasova@fpharm.uniba.sk.
Bioorg Med Chem Lett ; 27(11): 2345-2349, 2017 06 01.
Article em En | MEDLINE | ID: mdl-28438541
ABSTRACT
Biologically active Knoevenagel condensates (1-14) of diarylheptanoids 1,7-bis(3-methoxy-4-hydroxyphenyl)hepta-1,7-diene-3,5-dione and 1,7-bis(3-ethoxy-4-hydroxyphenyl)hepta-1,7-diene-3,5-dione, were synthesized and structurally characterized. Compounds 1-14 exhibited cytotoxicity against colon carcinoma cells, and their antiproliferative effect was associated with a significant decrease of multidrug resistance proteins. One of the underlying mechanisms of these effects is the reduction of intracellular and extracellular SOD enzymes by compounds 1, 12 and 14, which render the tumor cells more vulnerable to oxidative stress.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Diarileptanoides / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Diarileptanoides / Antineoplásicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article