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Mannich bases of 1,2,4-triazole-3-thione containing adamantane moiety: Synthesis, preliminary anticancer evaluation, and molecular modeling studies.
Milosev, Milorad Z; Jakovljevic, Katarina; Joksovic, Milan D; Stanojkovic, Tatjana; Matic, Ivana Z; Perovic, Milka; Tesic, Vesna; Kanazir, Selma; Mladenovic, Milan; Rodic, Marko V; Leovac, Vukadin M; Trifunovic, Snezana; Markovic, Violeta.
Afiliação
  • Milosev MZ; Faculty of Medicinal Science, University of Kragujevac, Kragujevac, Serbia.
  • Jakovljevic K; Faculty of Science, Department of Chemistry, University of Kragujevac, Kragujevac, Serbia.
  • Joksovic MD; Faculty of Science, Department of Chemistry, University of Kragujevac, Kragujevac, Serbia.
  • Stanojkovic T; Institute of Oncology and Radiology of Serbia, Belgrade, Serbia.
  • Matic IZ; Institute of Oncology and Radiology of Serbia, Belgrade, Serbia.
  • Perovic M; Institute for Biological Research "Sinisa Stankovic", Department of Neurobiology, University of Belgrade, Belgrade, Serbia.
  • Tesic V; Institute for Biological Research "Sinisa Stankovic", Department of Neurobiology, University of Belgrade, Belgrade, Serbia.
  • Kanazir S; Institute for Biological Research "Sinisa Stankovic", Department of Neurobiology, University of Belgrade, Belgrade, Serbia.
  • Mladenovic M; Faculty of Science, Department of Chemistry, University of Kragujevac, Kragujevac, Serbia.
  • Rodic MV; Faculty of Sciences, University of Novi Sad, Novi Sad, Serbia.
  • Leovac VM; Faculty of Sciences, University of Novi Sad, Novi Sad, Serbia.
  • Trifunovic S; Faculty of Chemistry, University of Belgrade, Belgrade, Serbia.
  • Markovic V; Faculty of Science, Department of Chemistry, University of Kragujevac, Kragujevac, Serbia.
Chem Biol Drug Des ; 89(6): 943-952, 2017 06.
Article em En | MEDLINE | ID: mdl-27933733
ABSTRACT
A series of 18 novel N-Mannich bases derived from 5-adamantyl-1,2,4-triazole-3-thione was synthesized and characterized using NMR spectroscopy and X-ray diffraction technique. All derivatives were evaluated for their anticancer potential against four human cancer cell lines. Several tested compounds exerted good cytotoxic activities on K562 and HL-60 cell lines, along with pronounced selectivity, showing lower cytotoxicity against normal fibroblasts MRC-5 compared to cancer cells. The effects of compounds 5b, 5e, and 5j on the cell cycle were investigated by flow cytometric analysis. It was found that these compounds cause the accumulation of cells in the subG1 and G1 phases of the cell cycle and induce caspase-dependent apoptosis, while the anti-angiogenic effects of 5b, 5e, and 5j have been confirmed in EA.hy926 cells using a tube formation assay. Further, the interaction of Bax protein with compound 5b was investigated by means of molecular modeling, applying the combined molecular docking/molecular dynamics approach.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tionas / Simulação de Acoplamento Molecular / Antineoplásicos Limite: Humans Idioma: En Revista: Chem Biol Drug Des Assunto da revista: BIOQUIMICA / FARMACIA / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tionas / Simulação de Acoplamento Molecular / Antineoplásicos Limite: Humans Idioma: En Revista: Chem Biol Drug Des Assunto da revista: BIOQUIMICA / FARMACIA / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article