Exploring the antileishmanial activity of N¹,N²-disubstituted-benzoylguanidines: synthesis and molecular modeling studies

Abstract

In this report, we describe the synthesis and evaluation of nine N¹,N²-disubstituted-benzoylguanidines against promastigotes and amastigotes forms of Leishmania amazonensis. The derivatives 2g and 2i showed low IC₅₀ values against promastigote form (90.8 ± 0.05 µM and 68.4 ± 0.03 µM, respectively), low cytotoxicity profile (CC₅₀ 396 ± 0.02 µM and 857.9 ± 0.06 µM) for peritoneal macrophages cells and SI of 5.5 and 12.5, respectively. Investigations about the mechanism of action of 2g and 2i showed that both compounds cause mitochondrial depolarization, increase in ROS levels, and generation of autophagic vacuoles on free promastigotes forms. These compounds were also capable of reducing the number of infected macrophages with amastigotes forms (59.5% ± 0.08% and 98.1% ± 0.46%) and the number of amastigotes/macrophages (79.80% ± 0.05% and 96.0% ± 0.16%), through increasing induction of microbicide molecule NO. Additionally, ADMET-Tox in silico predictions showed drug-like features and free of toxicological risks. The molecular docking studies with arginase and gp63 showed that relevant intermolecular interactions could explain the experimental results. Therefore, these results reinforce that benzoylguanidines could be a starting scaffold for the search for new antileishmanial drugs.

Communicated by Ramaswamy H. Sarma

Graphical Abstract

Keywords:

• Arginase
• gp63
• guanidine
• in silico studies
• trypanosomatids

Acknowledgements

The authors would like to thank the Laboratório Multiusuário de Análises Químicas do Instituto de Química - Unesp Araraquara for HR-MS analysis, as well the Multiuser Nuclear Magnetic Resonance Laboratory-RMNUEL/FINEP for NMR experiments.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001. Besides, it was supported by Conselho Nacional de Pesquisa (CNPq, Brazil).