Synthesis, cytotoxicity and antifungal activity of 5-nitro-thiophene-thiosemicarbazones derivatives

• Published in: Chemico-biological interactions 2017-06, Vol.272, p.172-181
• Main Authors: de Araújo Neto, Luiz Nascimento, do Carmo Alves de Lima, Maria, de Oliveira, Jamerson Ferreira, de Souza, Edson Rubhens, Buonafina, Maria Daniela Silva, Vitor Anjos, Mayara Nunes, Brayner, Fábio André, Alves, Luiz Carlos, Neves, Rejane Pereira, Mendonça-Junior, Francisco Jaime Bezerra
• Format: Article
• Language: English
• Subjects: Animals; Antifungal; Antifungal Agents - chemical synthesis; Antifungal Agents - chemistry; Antifungal Agents - toxicity; Candida; Candida - drug effects; Cell Survival - drug effects; Citotoxicity; Cryptococcus neoformans; Magnetic Resonance Spectroscopy; Mass Spectrometry; Mice; Mice, Inbred BALB C; Microbial Sensitivity Tests; Microscopy, Electron, Scanning; Spleen - cytology; Spleen - drug effects; Spleen - metabolism; Thiosemicarbazones; Thiosemicarbazones - chemical synthesis; Thiosemicarbazones - chemistry; Thiosemicarbazones - toxicity
• ISSN: 0009-2797; 1872-7786
• DOI: 10.1016/j.cbi.2017.05.005

In the present work, twelve N-substituted 2-(5-nitro-thiophene)-thiosemicarbazones derivatives (L1-12) were synthesized, characterized and their in vitro cytotoxic and antifungal activities were evaluated against Candida sp. and Cryptococcus neoformans. The probable mechanisms of action have been investigated by sorbitol and ergosterol assays. Additionally, ultrastructural study by Scanning Electron Microscopy was performed with the L10 compound. All compounds were obtained in good yield and their chemical structures were characterized on basis of their physico-chemical and Nuclear Magnetic Resonance - NMR, Spectrophotometric Absorption in the Infrared - IR and High-resolution Mass Spectrometry - HRMS data. The results showed that all strains were more sensitive to the compound L10 except Candida tropicalis URM 6551. On the other hand, the cytotoxicity assay by incorporation of tritiated thymidine showed moderate cytotoxic activity on L8 of the 50 μg/mLat which had the best MIC-cytotoxicity relationship. Concerning the study of the possible mechanism of action, the compounds were not able to bind to ergosterol in the membrane, do not act by inhibiting the synthesis of fungal cell wall (sorbitol assay). However, the Scanning Electron Microscopy - SEM analysis shows significant morphological changes in shape, size, number of cells and hyphae, and cell wall indicating a possible mechanism of action by inhibition of enzymes related to the ergosterol biosynthesis pathway. Our results demonstrate that N-substituted 2-(5-nitro-thiophene)-thiosemicarbazones derivatives are potential antifungal agents with activity associated with inhibition of enzymes related to biosynthesis of ergosterol. •Nine thiophene-thiosemicarbazones derivatives were synthesized and fully characterized.•All compounds showed fungicidal activity in low micromolar concentration.•All compounds are non-toxic at fungicidal concentrations.•Selected compound (L10) does not bind to ergosterol or inhibit the synthesis of fungal cell wall.•Ultrastructural analysis (SEM) suggests intereference in ergosterol biosynthesis pathway.