Publicações Selecionadas


Silva, I. R., Kronenberger, T., Gomes, E. C., César, I. C., Oliveira, R. B., Maltarollo, V. G. (2021). Improving the solubility of an antifungal thiazolyl hydrazone derivative by cyclodextrin complexation. European Journal of Pharmaceutical Sciences156, 105575. DOI: 10.1016/j.ejps.2020.105575



Andrade, M. M., Martins, L. C., Marques, G. V., Silva, C. A., Faria, G., Caldas, S., dos Santos, J. S. C., Leclercq, S. Y., Maltarollo, V. G., Ferreira, R. S., Oliveira, R. B. (2020). Synthesis of quinoline derivatives as potential cysteine protease inhibitors. Future medicinal chemistry12(7), 571-581. DOI: 10.4155/fmc-2019-0201

Asse Junior, L. R., Kronenberger, T., Magalhaes Serafim, M. S., Sousa, Y. V., Franco, I. D., Valli, M.,  Bolzani, V. S., Monteiro, G. C., Prates, J. L. B., Kroon, E. G., Mota, B. E. F., Ferreira, D. S., Oliveira, R. B., Maltarollo, V. G. (2020). Virtual screening of antibacterial compounds by similarity search of Enoyl-ACP reductase (FabI) inhibitors. Future medicinal chemistry12(1), 51-68. DOI: 10.4155/fmc-2019-0158



Serafim, M. S., Lavorato, S. N., Kronenberger, T., Sousa, Y. V., Oliveira, G. P., Dos Santos, S. G., Kroon, E. G., Maltarollo, V. G.,  Alves, R. J., Mota, B. E. (2019). Antibacterial activity of synthetic 1, 3‐bis (aryloxy) propan‐2‐amines against Gram‐positive bacteria. MicrobiologyOpen8(11), e814. DOI: 10.1002/mbo3.814



Lino, C. I., de Souza, I. G., Borelli, B. M., Matos, T. T. S., Teixeira, I. N. S., Ramos, J. P., Fagundes, E. M. S., Fernandes, P. O., Maltarollo, V. G., Johann, S., Oliveira, R. B. (2018). Synthesis, molecular modeling studies and evaluation of antifungal activity of a novel series of thiazole derivatives. European journal of medicinal chemistry151, 248-260. DOI: 10.1016/j.ejmech.2018.03.083



Braga, S. F. P., Martins, L. C., da Silva, E. B., Júnior, P. A. S., Murta, S. M. F., Romanha, A. J., Soh, W. T., Brandstetter, H., Oliveira, R. B. (2017). Synthesis and biological evaluation of potential inhibitors of the cysteine proteases cruzain and rhodesain designed by molecular simplification. Bioorganic & medicinal chemistry25(6), 1889-1900. DOI: 10.1016/j.bmc.2017.02.009

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