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Antichagasic, Leishmanicidal, and Trichomonacidal Activity of 2-Benzyl-5-nitroindazole-Derived Amines

Authors :
Vicente J. Arán
Alexandra Ibáñez-Escribano
Alicia Gómez-Barrio
José Antonio Escario
Patrícia Bernardino da Silva
Marcos Meuser Batista
Alfredo Meneses-Marcel
Juan José Nogal-Ruiz
Maria de Nazaré Correia Soeiro
José Cumella
Cristina Fonseca-Berzal
Nerea Vela
Sergio Sifontes-Rodríguez
Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
Instituto Nacional de Ciência e Tecnologia (Brasil)
Universidad Complutense de Madrid
Ministerio de Economía, Industria y Competitividad (España)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname
Publication Year :
2018

Abstract

Three different series of new 5-nitroindazole derivatives—1-(ω-aminoalkyl)-2-benzylindazolin-3-ones (series A; ten compounds), 3-(ω-aminoalkoxy)-2-benzylindazoles (series B; four compounds) and 3-alkylamino-2-benzylindazoles (series C; five compounds)—have been synthesized and evaluated against the protozoan parasites Trypanosoma cruzi, Leishmania amazonensis, and Trichomonas vaginalis: etiological agents of Chagas disease, cutaneous leishmaniasis, and trichomoniasis, respectively. Many indazoles of series A, B, and C were efficient against T. cruzi. Some compounds in series A, after successfully passing the preliminary screening for epimastigotes, exhibited activity values against amastigotes of several T. cruzi strains that were better than or similar to those shown by the reference drug benznidazole and displayed low nonspecific toxicity against mammalian cells. On the other hand, preliminary studies against promastigotes of L. amazonensis showed high leishmanicidal activity for some derivatives of series A and C. With regard to activity against T. vaginalis, some indazoles of series B and C were rather efficient against trophozoites of a metronidazole-sensitive isolate and showed low nonspecific toxicities toward Vero cell cultures. Additionally, some of these compounds displayed similar activity against metronidazole-sensitive and resistant isolates, showing the absence of cross-resistance between these derivatives and the reference drug.<br />This work was supported by the Spanish Ministry of Economy, Industry and Competitiveness (MINEICO; ref. SAF2015-66690-R), by the 911120 UCM-CEI Moncloa research group (E-Health Cluster), by the National Council for Scientific and Technological Development of Brazil (CNPq; ref. 301372/2015-2) and by the Fundaçao Carlos Chagas Filho de Amparo / Pesquisa do Estado do Rio de Janeiro (FAPERJ; ref. E02/2017). M.N.C.S. is a research fellow of CNPq and CNE. The authors thank the Program for Technological Development in Tools for Health (PDTIS-FIOCRUZ) for use of their facilities.

Details

ISSN :
18607187 and 20156669
Volume :
13
Issue :
12
Database :
OpenAIRE
Journal :
ChemMedChem
Accession number :
edsair.doi.dedup.....0b138a72a34ab6fa3a9879b631a01b5e