Produção Nacional
Revisado por pares
Interaction study with DNA/HSA, anti-topoisomerase IIα, cytotoxicity and in vitro antiproliferative evaluations and molecular docking of indole-thiosemicarbazone compounds
2023; Elsevier BV; Volume: 234; Linguagem: Inglês
10.1016/j.ijbiomac.2023.123606
ISSN1879-0003
AutoresÍris Trindade Tenório Jacob, Iranildo José da Cruz Filho, Josival Emanuel Ferreira Alves, Felipe de Melo Souza, Rafael David Souto de Azevedo, Diego Santa Clara Marques, Túlio Ricardo Couto de Lima Souza, Keriolaine Lima dos Santos, Maíra Galdino da Rocha Pitta, Moacyr Jesus Barreto de Melo Rêgo, Jamerson Ferreira de Oliveira, Sinara Mônica Vitalino de Almeida, Maria do Carmo Alves de Lima,
Tópico(s)Synthesis and biological activity
ResumoIn this work we will discuss the antiproliferative evaluation and the possible mechanisms of action of indole-thiosemicarbazone compounds LTs with anti-inflammatory activity, previously described in the literature. In this perspective, some analyzes were carried out, such as the study of binding to human serum albumin (HSA) and to biological targets: DNA and human topoisomerase IIα (topo). Antiproliferative study was performed with DU-145, Jukart, MCF-7 and T-47D tumor lines and J774A.1, besides HepG2 macrophages and hemolytic activity. In the HSA interaction tests, the highest binding constant was 3.70 × 106 M-1, referring to LT89 and in the fluorescence, most compounds, except for LT76 and LT87, promoted fluorescent suppression with the largest Stern-Volmer constant for the LT88 3.55 × 104. In the antiproliferative assay with DU-145 and Jurkat strains, compounds LT76 (0.98 ± 0.10/1.23 ± 0.32 μM), LT77 (0.94 ± 0.05/1.18 ± 0.08 μM) and LT87 (0.94 ± 0.12/0.84 ± 0.09 μM) stood out, due to their IC50 values mentioned above. With the MCF-7 and T-47D cell lines, the lowest IC50 was presented by LT81 with values of 0.74 ± 0.12 μM and 0.68 ± 0.10 μM, respectively, followed by the compounds LT76 and LT87. As well as the positive control amsacrine, the compounds LT76, LT81 and LT87 were able to inhibit the enzymatic action of human Topoisomerase IIα.
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