Synthesis, activity, and molecular modeling studies of 1,2,3-triazole derivatives from natural phenylpropanoids as new trypanocidal agents.


Journal

Chemical biology & drug design
ISSN: 1747-0285
Titre abrégé: Chem Biol Drug Des
Pays: England
ID NLM: 101262549

Informations de publication

Date de publication:
01 2020
Historique:
received: 22 05 2019
revised: 12 08 2019
accepted: 21 09 2019
pubmed: 1 10 2019
medline: 29 1 2021
entrez: 1 10 2019
Statut: ppublish

Résumé

The search for compounds with new structural scaffolds is an important tool to the discovery of new drugs against Chagas disease. We report herein the synthesis of 1,2,3-triazoles obtained from eugenol and di-hydroeugenol and their in vitro and in vivo trypanocidal activity. These derivatives were obtained by a three-step objective route and were suitably characterized by

Identifiants

pubmed: 31569301
doi: 10.1111/cbdd.13628
doi:

Substances chimiques

Biological Products 0
Cysteine Proteinase Inhibitors 0
Protozoan Proteins 0
Triazoles 0
Trypanocidal Agents 0
Cysteine Endopeptidases EC 3.4.22.-
cruzipain EC 3.4.22.51

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

124-129

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Références

Abrão, P. H. O., Pizi, R. B., Souza, T. B., Silva, N. C., Fregnan, A. M., Silva, F. N., … Carvalho, D. T. (2015). Synthesis and biological evaluation of new eugenol Mannich bases as promising antifungal agents. Chemical Biology & Drug Design, 86, 459-465. https://doi.org/10.1111/cbdd.12504
Andrade, P., Galo, O. A., Carvalho, M. R., Lopes, C. D., Carneiro, Z. A., Sesti-Costa, R., … Carvalho, I. (2015). 1,2,3-Triazole-based analogue of benznidazole displays remarkable activity against Trypanosoma cruzi. Bioorganic and Medicinal Chemistry, 23, 6815-6826. https://doi.org/10.1016/j.bmc.2015.10.008
Brak, K., Kerr, I. D., Barrett, K. T., Fuchi, N., Debnath, M., Ang, K., … Ellman, J. A. (2010). Nonpeptidic tetrafluorophenoxymethyl ketone cruzain inhibitors as promising new leads for Chagas disease chemotherapy. Journal of Medicinal Chemistry, 53, 1763-1773. https://doi.org/10.1021/jm901633v
Carvalho, I., Andrade, P., Campo, V. L., Guedes, P. M. M., Sesti-Costa, R., Silva, J. S., … Field, R. A. (2010). ‘Click chemistry’ synthesis of a library of 1,2,3-triazole-substituted galactose derivatives and their evaluation against Trypanosoma cruzi and its cell surface trans-sialidase. Bioorganic & Medicinal Chemistry, 18, 2412-2427. https://doi.org/10.1016/j.bmc.2010.02.053
Cazelli, D. S. P., Barroso, M. E. S., Pizi, R. B., Orlandi, M., Souza, T. B., Carvalho, D. T., … Endringer, D. C. (2017). The relationship between the antimicrobial activity of eugenol and the LPETG peptide structure and associated analysis for docking purposes. Chemical Papers, 71, 1877-1886. https://doi.org/10.1007/s11696-017-0181-0
da Silva, E. N., Menna-Barreto, R. F. S., Pinto, M. D. C. F. R., Silva, R. S. F., Teixeira, D. V., de Souza, M. C. B. V., … Pinto, A. V. (2008). Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi. European Journal of Medicinal Chemistry, 43, 1774-1780. https://doi.org/10.1016/j.ejmech.2007.10.015
Dai, J. P., Zhao, X. F., Zeng, J., Wan, Q. Y., Yang, J. C., Li, W. Z., … Li, K. S. (2013). Drug screening for autophagy inhibitors based on the dissociation of Beclin1-Bcl2 complex using BiFC technique and mechanism of eugenol on anti-influenza a virus activity. PLoS ONE, 8, 1-16. https://doi.org/10.1371/journal.pone.0061026
Daniel, A. N., Sartoretto, S. M., Schmidt, G., Caparroz-Assef, S. M., Bersani-Amado, C. A., & Cuman, R. K. N. (2009). Anti-inflammatory and antinociceptive activities of eugenol essential oil in experimental animal models. Brazilian Journal of Pharmacognosy, 19, 212-217. https://doi.org/10.1590/S0102-695X2009000200006
Deobald, A. M., Camargo, L. R. S., Alves, D., Zukerman-Schpector, J., Corrêa, A. G., & Paixão, M. W. (2011). Click chemistry: An efficient synthesis of heterocycles substituted with steroids, saponins, and digitalis analogues. Synthesis, 24, 4003-4010.
Freitas, L. B. O., Ruela, F. A., Pereira, G. R., Alves, R. B., Freitas, R. P., & Santos, L. J. (2011). The "click" reaction in the synthesis of 1,2,3-triazoles: Chemical aspects and applications. Química Nova, 34, 1791-1804. https://doi.org/10.1590/S0100-40422011001000012
Gülçin, I. (2011). Antioxidant activity of eugenol: A structure-activity relationship study. Journal of Medicinal Food, 14, 975-985. https://doi.org/10.1089/jmf.2010.0197
Jin, C., Nagasawa, H., Shimamura, M., Uto, Y., Inayama, S., Takeuchi, Y., … Hori, H. (2004). Angiogenesis inhibitor TX-1898: Synthesis of the enantiomers of sterically diverse haloacetylcarbamoyl-2-nitroimidazole hypoxic cell radiosensitizers. Bioorganic & Medicinal Chemistry, 12, 4917-4927. https://doi.org/10.1016/j.bmc.2004.06.039
Machado, M., Dinis, A. M., Salgueiro, L., Custódio, J. B. A., Cavaleiro, C., & Sousa, M. C. (2011). Anti-Giardia activity of Syzygium aromaticum essential oil and eugenol: Effects on growth, viability, adherence and ultrastructure. Experimental Parasitology, 127, 732-739. https://doi.org/10.1016/j.exppara.2011.01.011
Manikandan, P., Senthil, R. M., Priyadarsini, R. V., Vinothini, G., & Nagini, S. (2010). Eugenol induces apoptosis and inhibits invasion and angiogenesis in a rat model of gastric carcinogenesis induced byMNNG. Life Science, 86, 936-941. https://doi.org/10.1016/j.lfs.2010.04.010
Porta, E. O. J., Jäger, S. N., Nocito, I., Lepesheva, G. I., Serra, E. C., Tekwani, B. L., & Labadie, G. R. (2017). Antitrypanosomal and antileishmanial activity of prenyl-1,2,3-triazoles. MedChemComm, 8, 1015-1021. https://doi.org/10.1039/c7md00008a
Shao, Y., Molnar, L. F., Jung, Y., Kussmann, J., Ochsenfeld, C., Brown, S. T., … Head-Gordon, M. (2006). Advances in methods and algorithms in a modern quantum chemistry program package. Physical Chemistry Chemical Physics, 8, 3172-3191. https://doi.org/10.1039/B517914A
Souza, T. B., Brito, K. M. O., Silva, N. C., Rocha, R. P., Sousa, G. F., Duarte, L. P., … Dias, D. F. (2016). New eugenol glucoside-based derivative shows fungistatic and fungicidal activity against opportunistic Candida glabrata. Chemical Biology & Drug Design, 87, 83-90. https://doi.org/10.1111/cbdd.12625
Souza, T. B., Orlandi, M., Coelho, L. F. L., Malaquias, L. C. C., Dias, A. L. T., Carvalho, R. R., … Carvalho, D. T. (2014). Synthesis and in vitro evaluation of antifungal and cytotoxic activities of eugenol glycosides. Medicinal Chemistry Research, 23, 496-502. https://doi.org/10.1111/cbdd.12625
Souza, T. B., Raimundo, P. O. B., Andrade, S. F., Hipólito, T. M. M., Silva, N. C., Dias, A. L. T. D., … Dias, D. F. (2015). Synthesis and antimicrobial activity of 6-triazolo-6-deoxy eugenol glucosides. Carbohydrate Research, 410, 1-8. https://doi.org/10.1016/j.carres.2015.04.002
Yadav, M. K., Chae, S. W., Im, J. G., Chung, J. W., & Song, J. J. (2015). Eugenol: A phyto-compound effective against methicillin-resistant and methicillin-sensitive Staphylococcus aureus clinical strain biofilms. PLoS ONE, 10, 1-21. https://doi.org/10.1371/journal.pone.0119564

Auteurs

Thiago Belarmino de Souza (TB)

Escola de Farmácia, Universidade Federal de Ouro Preto, Ouro Preto, Brazil.

Ivo Santana Caldas (IS)

Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas, Brazil.

Favero Reisdorfer Paula (FR)

Universidade Federal do Pampa, Uruguaiana, Brazil.

Camila Coelho Rodrigues (CC)

Universidade Federal do Pampa, Uruguaiana, Brazil.

Diogo Teixeira Carvalho (DT)

Faculdade de Ciências Farmacêuticas, Universidade Federal de Alfenas, Alfenas, Brazil.

Danielle Ferreira Dias (DF)

Instituto de Química, Universidade Federal de Alfenas, Alfenas, Brazil.

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