Synthesis of Novel Benzylic 1,2,3-triazole-4-carboxamides and their in vitro Activity Against Clinically Common Fungal Species

Authors

  • Davir González-Calderón Universidad Autónoma del Estado de México
  • Ricardo García-Monroy Universidad Autónoma del Estado de México
  • Alejandra Ramírez-Villalva Universidad Autónoma del Estado de México
  • Salvador Mastachi-Loza Universidad Autónoma del Estado de México
  • José G. Aguirre-de Paz Universidad Autónoma del Estado de México
  • Aydee Fuentes-Benítes Universidad Autónoma del Estado de México
  • Carlos González-Romero Universidad Autónoma del Estado de México

DOI:

https://doi.org/10.29356/jmcs.v65i2.1457

Keywords:

1,2,3-Triazoles, antifungal activity, 1,3-dipolar cycloaddition, Rhizopus oryzae

Abstract

Abstract. A library of novel benzylic 1,2,3-triazole-4-carboxamides (3a-m) were obtained with acceptable yields via a one-pot procedure. The series of compounds was screened for fungicidal activity and evaluated in vitro against four filamentous fungi and four Candida species. The former consisted of Aspergillus fumigatus, Trichosporon cutaneum, Rhizopus oryzae and Mucor hiemalis, and the latter C. krusei, C. albicans, C. utilis and C. glabrata. According to the in vitro assays, 3d and 3e were the most efficient fungicidal agents (of all the test compounds) against R. oryzae, even better than the reference drug (itraconazole). Thus, 3d and 3e represent important scaffolds that can be modified to increase antifungal activity. Additionally, they are candidates for complementary studies on the inhibition of clinical infections produced by Rhizopus spp. strains.

 

Resumen. Se obtuvo una librería de nuevos bencil 1,2,3-triazoles-4-carboxamidas (3a-m) con rendimientos aceptables mediante un procedimiento one-pot. La serie de compuestos se seleccionó para determinar la actividad fungicida llevando a cabo una evaluación in vitro contra cuatro hongos filamentosos y cuatro especies de Candida. Los primeros consistieron en Aspergillus fumigatus, Trichosporon cutaneum, Rhizopus oryzae y Mucor hiemalis, mientras que para las segundas especies, esta fueron C. krusei, C. albicans, C. utilis y C. glabrata. Según los ensayos in vitro, 3d y 3e fueron los agentes fungicidas más eficaces (de todos los compuestos de prueba) contra R. oryzae, incluso mejores que el fármaco de referencia (itraconazol). Por tanto, 3d y 3e representan importantes núcleos que podrían modificarse para aumentar la actividad antifúngica, siendo excelentes candidatos para estudios complementarios sobre la inhibición de infecciones clínicas producidas por Rhizopus spp.

Downloads

Download data is not yet available.

Author Biographies

Davir González-Calderón, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Ricardo García-Monroy, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Departamento de Microbiología, Facultad de Química, Universidad Autónoma del Estado de México

Alejandra Ramírez-Villalva, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Departamento de Microbiología, Facultad de Química, Universidad Autónoma del Estado de México

Salvador Mastachi-Loza, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Departamento de Microbiología, Facultad de Química, Universidad Autónoma del Estado de México

José G. Aguirre-de Paz, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Aydee Fuentes-Benítes, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

Carlos González-Romero, Universidad Autónoma del Estado de México

Departamento de Química Orgánica, Facultad de Química

References

Rodrigues, M. L.; Nosanchuk, J. D. PLoS Negl. Trop. Dis. 2020, 14, e0007964. https://doi.org/10.1371/journal.pntd.0007964 DOI: https://doi.org/10.1371/journal.pntd.0007964

Köhler, J. R.; Casadevall, A.; Perfect, J. Cold Spring Harb. Perspect. Med. 2015, 5, a019273. https://doi.org/10.1101/cshperspect.a019273 DOI: https://doi.org/10.1101/cshperspect.a019273

Köhler, J. R.; Hube, B.; Puccia, R.; Casadevall, A.; Perfect, J. R., Chapter 39: Fungi that Infect Humans. In: The Fungal Kingdom. Heitman, J.; Howlett, B. J.; Crous, P. W.; Stukenbrock, E. H.; James, T. Y.; Gow, N. A. R. (Ed)., American Society for Microbiology 2017, e-ISBN: 9781555819583. https://doi.org/10.1128/microbiolspec.FUNK-0014-2016 DOI: https://doi.org/10.1128/microbiolspec.FUNK-0014-2016

Dheer, D.; Singh, V.; Shankar, R. Bioorg. Chem. 2017, 71, 30-54. https://doi.org/10.1016/j.bioorg.2017.01.010 DOI: https://doi.org/10.1016/j.bioorg.2017.01.010

Kharb, R.; Sharma, P. C.; Yar, M. S. J. Enzym. Inhib. Med. Chem. 2011, 26, 1–21. https://doi.org/10.3109/14756360903524304 DOI: https://doi.org/10.3109/14756360903524304

de Carvalho da Silva, F.; Cardoso, M. F. C.; Ferreira, P. G.; Ferreira V. F. Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles. In: Dehaen W., Bakulev V. (eds) Chemistry of 1,2,3-triazoles. Topics in Heterocyclic Chemistry, vol 40, Springer, Cham, 2014. Online ISBN 978-3-319-07962-2. https://doi.org/10.1007/7081_2014_124 DOI: https://doi.org/10.1007/7081_2014_124

Massarotti, A.; Aprile, S.; Mercalli, V.; Del Grosso, E.; Grosa, G.; Sorba, G.; Tron, G. C. Chem. Med. Chem. 2014, 9, 2497–2508. https://doi.org/10.1002/cmdc.201402233 DOI: https://doi.org/10.1002/cmdc.201402233

Agalave, S. G.; Maujan, S. R.; Pore, V. S., Chem. Asian J. 2011, 6, 2696–2718. https://doi.org/10.1002/asia.201100432 DOI: https://doi.org/10.1002/asia.201100432

Howard, K. C.; Dennis, E. K.; Watt, D. S.; Garneau-Tsodikova, S. A. Chem. Soc. Rev. 2020, 49, 2426-2480. https://doi.org/10.1039/c9cs00556k DOI: https://doi.org/10.1039/C9CS00556K

Rani, A.; Singh, G.; Singh, A.; Maqbool, U.; Kaur, G.; Singh, J. RSC Adv. 2020, 10, 5610-5635. https://doi.org/10.1039/C9RA09510A DOI: https://doi.org/10.1039/C9RA09510A

Lass-Flörl, C. Drugs 2011, 71, 2405–2419. https://doi.org/10.2165/11596540-000000000-00000 DOI: https://doi.org/10.2165/11596540-000000000-00000

Nett, J. E.; Andes, D. R. Infect. Dis. Clin. North Am. 2016, 30, 51–83. https://doi.org/10.1016/j.idc.2015.10.012 DOI: https://doi.org/10.1016/j.idc.2015.10.012

Miceli, M. H.; Kauffman, C. A. Clin. Infect. Dis. 2015, 61, 1558–1565. https://doi.org/10.1093/cid/civ571 DOI: https://doi.org/10.1093/cid/civ571

Chang, Y. L.; Yu, S. J.; Heitman, J.; Wellington, M.; Chen, Y. L. Virulence 2017, 8, 222–236. https://doi.org/10.1080/21505594.2016.1257457 DOI: https://doi.org/10.1080/21505594.2016.1257457

Seyedmousavi, S.; Verweij, P. E.; Mouton, J. W. Expert Rev. Anti. Infect. Ther. 2015, 13, 9–27. https://doi.org/10.1586/14787210.2015.990382 DOI: https://doi.org/10.1586/14787210.2015.990382

Peyton, L. R.; Gallagher, S.; Hashemzadeh, M. Drugs Today (Barc) 2015, 51, 705–718. https://doi.org/10.1358/dot.2015.51.12.2421058 DOI: https://doi.org/10.1358/dot.2015.51.12.2421058

Chitasombat, M. N.; Kontoyiannis, D. P. Expert Opin. Pharmacother. 2015, 16, 1543–1558. https://doi.org/10.1517/14656566.2015.1057500 DOI: https://doi.org/10.1517/14656566.2015.1057500

Revie, N. M.; Iyer, K. R.; Robbins, N.; Cowen, L. E. Curr. Opin. Microbiol. 2018, 45, 70–76. https://doi.org/10.1016/j.mib.2018.02.005 DOI: https://doi.org/10.1016/j.mib.2018.02.005

Perlin, D. S.; Rautemaa-Richardson, R.; Alastruey-Izquierdo, A. Lancet Infect. Dis. 2017, 17, 383–392. https://doi.org/10.1016/S1473-3099(17)30316-X DOI: https://doi.org/10.1016/S1473-3099(17)30316-X

Beardsley, J.; Halliday, C. L.; Chen, S.; Sorrell, T. C. Future Microbiol. 2018, 13, 1175–1191. https://doi.org/10.2217/fmb-2018-0059 DOI: https://doi.org/10.2217/fmb-2018-0059

Lopez-Ribot, J. L.; Wiederhold, N. P.; Patterson T. F., Fungal Drug Resistance: Azoles. In: Mayers, D.; Sobel, J.; Ouellette, M.; Kaye, K.; Marchaim, D. (eds), Antimicrobial Drug Resistance. Springer, Cham, 2017, Online ISBN 978-3-319-46718-4, https://doi.org/10.1007/978-3-319-46718-4_27 DOI: https://doi.org/10.1007/978-3-319-46718-4_27

Caramalho, R.; Tyndall, J. D. A.; Monk, B. C. Sci Rep. 2017, 7, 15898. https://doi.org/10.1038/s41598-017-16123-9 DOI: https://doi.org/10.1038/s41598-017-16123-9

Dannaoui, E. Int. J. Antimicrob. Agents 2017, 50, 617-621. https://doi.org/10.1016/j.ijantimicag.2017.08.010 DOI: https://doi.org/10.1016/j.ijantimicag.2017.08.010

Odds, F. C.; Brown, A. J. P.; Gow, N. A. R. Trends Microbiol. 2003, 11, 272-279. https://doi.org/10.1016/s0966-842x(03)00117-3 DOI: https://doi.org/10.1016/S0966-842X(03)00117-3

Balding, P. R.; Porro, C. S., Munro, A. W.; Visser, S. P. J. Phys. Chem. A 2008, 112, 12911–12918. https://doi.org/10.1021/jp802087w DOI: https://doi.org/10.1021/jp802087w

Zhang, Y.; Damu, G. L. V.; Cui, S. F.; Mi, J. L.; Tangadanchu, V. K. R.; Zhou, C. H. Med. Chem. Commun., 2017, 8, 1631-1639. https://doi.org/10.1039/C7MD00112F DOI: https://doi.org/10.1039/C7MD00112F

Mast, N.; Zheng, W.; Stout, C. D.; Pikuleva, I. A. Molecular Pharmacology 2013, 84, 86-94; https://doi.org/10.1124/mol.113.085902 DOI: https://doi.org/10.1124/mol.113.085902

Kaushik, C. P.; Luxmi, R.; Kumar, M.; Singh, D.; Kumar, K.; Pahwa, A. Synth. Commun. 2019, 49, 118-128. https://doi.org/10.1080/00397911.2018.1544371 DOI: https://doi.org/10.1080/00397911.2018.1544371

Thanh, N. D.; Hai, D. S.; Bich, V. T. N.; Hien, P. T. T.; Duyen, N. T. K.; Mai, N. T.; Dung, T. T.; Toan, V. N.; Van, H. T. K.; Dang, L. H.; Toan, D. N.; Van, T. T. T. Eur. J. Med. Chem. 2019, 167, 454-471. https://doi.org/10.1016/j.ejmech.2019.01.060 DOI: https://doi.org/10.1016/j.ejmech.2019.01.060

Fu, N.; Wang, S.; Zhang, Y.; Zhang, C.; Yang, D.; Weng, L.; Zhao, B.; Wang, L. Eur. J. Med. Chem. 2017, 136, 596-602, https://doi.org/10.1016/j.ejmech.2017.05.001 DOI: https://doi.org/10.1016/j.ejmech.2017.05.001

Aneja, B.; Irfan, M.; Kapil, C.; Jairajpuri, M. A.; Maguire, R.; Kavanagh, K.; Rizvi, M. M. A.; Manzoor, N.; Azam, A.; Abid, M. Org. Biomol. Chem. 2016, 14, 10599-10619. https://doi.org/10.1039/C6OB01718E DOI: https://doi.org/10.1039/C6OB01718E

Dai, Z. H.; Chen, Y. F.; Zhang, M.; Li, S. K.; Yang, T. T.; Shen, L.; Wang, J. X.; Qian, S. S.; Zhu, H. L.; Ye, Y. H. Org. Biomol. Chem. 2015, 13, 477-486. https://doi.org/10.1039/C4OB01758G DOI: https://doi.org/10.1039/C4OB01758G

Ramírez-Villalva, A.; González-Calderón, D.; Rojas-García, R. I.; González-Romero, C.; Tamaríz-Mascarúa, J.; Morales-Rodríguez, M.; Zavala-Segovia, N.; Fuentes-Benítes, A. Med. Chem. Commun. 2017, 8, 2258–2262, https://doi.org/10.1039/c7md00442g DOI: https://doi.org/10.1039/C7MD00442G

González-Calderón, D.; Mejía-Dionicio, M. G.; Morales-Reza, M. A.; Ramírez-Villalva, A.; Morales-Rodríguez, M.; Jauregui-Rodríguez, B.; Díaz-Torres, E.; González-Romero, C.; Fuentes-Benítes, A. Eur. J. Med. Chem. 2016, 112, 60-65. https://doi.org/10.1016/j.ejmech.2016.02.013 DOI: https://doi.org/10.1016/j.ejmech.2016.02.013

González-Calderón, D.; Mejía-Dionicio, M. G.; Morales-Reza, M. A.; Aguirre-de Paz, J. G.; Ramírez-Villalva, A.; Morales-Rodríguez, M.; Fuentes-Benítes, A.; González-Romero, C. Bioorg. Chem. 2016, 69, 1–6, https://doi.org/10.1016/j.bioorg.2016.09.003 DOI: https://doi.org/10.1016/j.bioorg.2016.09.003

Ballari, M. S.; Herrera-Cano, N.; Lopez, A. G.; Wunderlin, D. A.; Feresín, G. E.; Santiago, A. N. J. Agric. Food Chem. 2017, 65, 10325–10331. https://doi.org/10.1021/acs.jafc.7b04130 DOI: https://doi.org/10.1021/acs.jafc.7b04130

Brand, S.; Ko, E. J.; Viayna, E.; Thompson, S.; Spinks, D.; Thomas, M.; Sandberg, L.; Marco, M.; Miles, T. J.; Read, K. D.; Gilbert, I. H. J. Med. Chem. 2017, 60, 7284–7299. https://doi.org/10.1021/acs.jmedchem.7b00463 DOI: https://doi.org/10.1021/acs.jmedchem.7b00463

Shaikh, M. H.; Subhedar, D. D.; Nawale, L.; Sarkar, D.; Khan, F. A. K.; Sangshetti, J. N.; Shingate, B. B. Med. Chem. Commun. 2015, 6, 1104-1116. https://doi.org/10.1039/C5MD00057B DOI: https://doi.org/10.1039/C5MD00057B

Kamal, A.; Rao, A. V. S.; Vishnuvardhan, M. V. P. S.; Reddy, T. S.; Swapna, K.; Bagul, C.; Reddy, N. V. S.; Srinivasulu, V. Org. Biomol. Chem. 2015, 13, 4879-4895. https://doi.org/10.1039/C5OB00232J DOI: https://doi.org/10.1039/C5OB00232J

Irfan, M.; Alam, S.; Manzoor, N.; Abid, M. PLoS ONE 2017, 12, e0175710. https://doi.org/10.1371/journal.pone.0175710 DOI: https://doi.org/10.1371/journal.pone.0175710

Shaikh, M. H.; Subhedar, D. D.; Khan, F. A. K.; Sangshetti, J. N.; Shingate, B. B. Chin. Chem. Lett. 2016, 27, 295-301. https://doi.org/10.1016/j.cclet.2015.11.003 DOI: https://doi.org/10.1016/j.cclet.2015.11.003

National Committee for Clinical Laboratory Standards Institute (CLSI), Document M38-A2: Reference Method for Broth Dilution Antifungal Susceptibility Testing of Filamentous Fungi, Approved Standard, Second Edition, Clinical and Laboratory Standards Institute, Wayne, PA, 2002.

Barry, A. L. An overview of the Clinical and Laboratory Standards Institute (CLSI) and its impact on antimicrobial susceptibility tests, in: Schwalbe, R.; Steele-Moore, L.; Goodwin, A.C. (Eds.), Antimicrobial Susceptibility Testing Protocols, CRC Press Taylor & Francis Group, Florida, 2007, 1-6. ISBN: 9780824741006. DOI: https://doi.org/10.1201/9781420014495.ch1

Espinel-Ingroff, A.; Canton, E. Antifungal susceptibility testing of filamentous fungi, in: Schwalbe, R.; Steele-Moore, L.; Goodwin, A.C. (Eds.), Antimicrobial Susceptibility Testing Protocols, CRC Press Taylor & Francis Group, Florida, 2007, 209-241. ISBN: 9780824741006. DOI: https://doi.org/10.1201/9781420014495.ch10

National Committee for Clinical and Laboratory Standards Institute (CLSI), M27-A3: Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts, Approved Standard, Third Edition, Clinical and Laboratory Standards Institute, Wayne, PA, 2008. ISBN: 1-56238-666-2.

Espinel-Ingroff, A.; Cantón, E. Antifungal susceptibility testing of yeasts, in: Schwalbe, R.; Steele-Moore, L.; Goodwin, A. C. (Eds.), Antimicrobial Susceptibility Testing Protocols, CRC Press Taylor & Francis Group, Florida, 2007, 173-208. ISBN: 9780824741006. DOI: https://doi.org/10.1201/9781420014495.ch9

Fothergill, A. W. Antifungal Susceptibility Testing: Clinical Laboratory and Standards Institute (CLSI) methods, in: G.S. Hall (Ed.), Interactions of Yeasts, Moulds, and Antifungal Agents. How to Detect Resistance, Springer Science-Business Media, 2012, 65-74. https://doi.org/10.1007/978-1-59745-134-5_2 DOI: https://doi.org/10.1007/978-1-59745-134-5_2

Vigezzi, C.; Riera, F. O.; Caeiro, J. P.; Sotomayor, C. E. Rev. Argent. Microbiol. 2020, In Press, https://doi.org/10.1016/j.ram.2020.06.003 DOI: https://doi.org/10.1016/j.ram.2020.06.003

Choi, S.; Song, J. S.; Woo, J. H.; Kim, S. H. Mycoses 2019, 62, 1006-14. https://doi.org/10.1111/myc.12994 DOI: https://doi.org/10.1111/myc.12994

Aguirre-De Paz, J. G.; González-Calderón, D.; Fuentes-Benítes, A.; González-Romero, C. Tet Lett. 2018, 59, 1760–1762. https://doi.org/10.1016/j.tetlet.2018.03.075 DOI: https://doi.org/10.1016/j.tetlet.2018.03.075

Vargas-Herrera, N.; Saavedra-Velasco, M.; Pichardo-Rodriguez, R. Acta Méd. Peru. 2020, 36, 287-290. DOI: https://doi.org/10.35663/amp.2019.364.903

Valdés, T. G. E.; Martínez, B. M. E.; Morayta, R. C. A. R. R. Rev. Latin. Infect. Pediatr. 2020, 33, 49-56. https://doi.org/10.35366/92386 DOI: https://doi.org/10.35366/92386

×

Additional Files

Published

2021-02-22

Issue

Section

Regular Articles
x

Similar Articles

<< < 7 8 9 10 11 12 13 14 15 16 > >> 

You may also start an advanced similarity search for this article.

Loading...