%0 Journal Article %1 RN19 %A Aguilera-Venegas, B. %A Olea-Azar, C. %A Norambuena, E. %A Aran, V.J. %A Mendizabal, F. %A Lapier, M. %A Maya, J.D. %A Kemmerling, U. %A Lopez-Munoz, R. %D 2011 %I 2010 Elsevier B.V. %J Spectrochimica Acta Part a-Molecular and Biomolecular Spectroscopy %K anion, behavior binding-site, chagas chagas-disease, complexes, crystal-structure, disease, dqcauchile epimastigote, esr, glutathione-reductase, modeling, molecular nifurtimox, nitro nitroquinoxaline, radical-anion, reductase, superoxide trypanothione trypomastigote, %N 3 %P 1004-1012 %R 10.1016/j.saa.2010.12.017 %T Esr, Electrochemical, Molecular Modeling and Biological Evaluation of 4-Substituted and 1,4-Disubstituted 7-Nitroquinoxalin-2-Ones as Potential Anti-Trypanosoma Cruzi Agents %U /brokenurl#<Go to ISI>://WOS:000288046600012 %V 78 %X Electrochemical and ESR studies were carried out in this work with the aim of characterizing the reduction mechanisms of 4-substituted and 1,4-disubstituted 7-nitroquinoxalin-2-ones by means of cyclic voltammetry in DMSO as aprotic solvent. Two reduction mechanisms were found for these compounds: the first, for compounds bearing a labile hydrogen by following a self-protonation mechanism (ECE steps), and the second, for compounds without labile hydrogen, based on a purely electrochemical reduction mechanism (typical of nitroheterocycles). The electrochemical results were corroborated using ESR spectroscopy allowing us to propose the hyperfine splitting pattern of the nitro-radical, which was later corroborated by the ESR simulation spectra. All these compounds were assayed as growth inhibitors against Trypanosoma cruzi: first, on the non-proliferative (and infective) form of the parasite (trypomastigote stage), and then, the ones that displayed activity, were assayed on the non-infective form (epimastigote stage). Thus, we found four new compounds highly active against T. cruzi. Finally, molecular modeling studies suggest the inhibition of the trypanothione reductase like one of the possible mechanisms involved in the trypanocidal action.

@article{RN19, abstract = {Electrochemical and ESR studies were carried out in this work with the aim of characterizing the reduction mechanisms of 4-substituted and 1,4-disubstituted 7-nitroquinoxalin-2-ones by means of cyclic voltammetry in DMSO as aprotic solvent. Two reduction mechanisms were found for these compounds: the first, for compounds bearing a labile hydrogen by following a self-protonation mechanism (ECE steps), and the second, for compounds without labile hydrogen, based on a purely electrochemical reduction mechanism (typical of nitroheterocycles). The electrochemical results were corroborated using ESR spectroscopy allowing us to propose the hyperfine splitting pattern of the nitro-radical, which was later corroborated by the ESR simulation spectra. All these compounds were assayed as growth inhibitors against Trypanosoma cruzi: first, on the non-proliferative (and infective) form of the parasite (trypomastigote stage), and then, the ones that displayed activity, were assayed on the non-infective form (epimastigote stage). Thus, we found four new compounds highly active against T. cruzi. Finally, molecular modeling studies suggest the inhibition of the trypanothione reductase like one of the possible mechanisms involved in the trypanocidal action. }, added-at = {2019-12-04T03:57:35.000+0100}, author = {Aguilera-Venegas, B. and Olea-Azar, C. and Norambuena, E. and Aran, V.J. and Mendizabal, F. and Lapier, M. and Maya, J.D. and Kemmerling, U. and Lopez-Munoz, R.}, biburl = {https://www.bibsonomy.org/bibtex/27df4e7b925ce1deb78b45b39e3729c6f/dqcauchile}, doi = {10.1016/j.saa.2010.12.017}, interhash = {d91cf0acc518a680894bb16655b4132f}, intrahash = {7df4e7b925ce1deb78b45b39e3729c6f}, issn = {1386-1425}, journal = {Spectrochimica Acta Part a-Molecular and Biomolecular Spectroscopy}, keywords = {anion, behavior binding-site, chagas chagas-disease, complexes, crystal-structure, disease, dqcauchile epimastigote, esr, glutathione-reductase, modeling, molecular nifurtimox, nitro nitroquinoxaline, radical-anion, reductase, superoxide trypanothione trypomastigote,}, number = 3, pages = {1004-1012}, publisher = {2010 Elsevier B.V.}, timestamp = {2019-12-04T03:58:17.000+0100}, title = {Esr, Electrochemical, Molecular Modeling and Biological Evaluation of 4-Substituted and 1,4-Disubstituted 7-Nitroquinoxalin-2-Ones as Potential Anti-Trypanosoma Cruzi Agents}, type = {Journal Article}, url = {/brokenurl#<Go to ISI>://WOS:000288046600012}, volume = 78, year = 2011 }