학술논문
Synthesis, antioxidant and antitumoral activity of new 5′-arylchalcogenyl-3′-N-(E)-feruloyl-3′, 5′-dideoxy-amino-thymidine (AFAT) derivatives.
Document Type
Article
Author
Leal, Julliano G.; Piccoli, Bruna Candia; Oliveira, Cláudia Sirlene; D'Avila da Silva, Fernanda; Omage, Folorunsho Bright; Rocha, João Batista Teixeira da; Sonego, Mariana Souza; Segatto, Natália Vieira; Seixas, Fabiana Kommling; Collares, Tiago Veiras; da Silva, Rafael Santos; Sarturi, Joelma Menegazzi; Dornelles, Luciano; Faustino, Maria Amparo F.; Rodrigues, Oscar E. D.
Source
Subject
*NEPHROTOXICOLOGY
*HEPATOTOXICOLOGY
*ANTIOXIDANTS
*CHEMICAL yield
*IN vivo studies
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Language
ISSN
1144-0546
Abstract
The synthesis of a new class of 5′-arylchalcogenyl-3′-N-(E)-feruloyl-3′-amino-3′-deoxythymidine (AFAT) derivatives is disclosed. The compounds were obtained in good yields by an amidation reaction employing soft conditions. Both antitumoral activity against bladder carcinoma cells T24 and the antioxidant effect of the new derivatives were assessed. The results obtained demonstrated a notable inhibition of TBARS production and the DPPH scavenging activity compared with the commercial standards or the precursor building blocks. Additionally, the tellurium AFAT derivatives showed prominent antiproliferative activities. The in vivo studies revealed that the mice group treated with AFAT derivatives kept a normal healthy condition after 1 week of treatment and no kidney or liver toxicity was observed in the in vivo biochemical assays. The in silico evaluation corroborated the experimental results and demonstrated a prominent ability of these compounds to be employed as multitarget drugs. [ABSTRACT FROM AUTHOR]