Reveals effectiveness of new 4-carboxylate-1,2,3-triazines against parasitic infections, suggesting potential therapy alternatives.
= 0.46 μM) similar to miltefosine against promastigotes of L. mexicana, and 1,2,3-triazine (2i) reduced parasitemia by up to 70 % in an in vivo mouse model. These results are the first report of 4-carboxylate-1,2,3-triazine 1-oxides and their deoxygenated and reduced analogs as trypanocidal and leishmanicidal agents, encouraging their use for the development of new therapeutic alternatives against these neglected parasitic diseases.
No takes yet. Share an insight, caveat, or question.
Navarrete-Carriola et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: