# Structural analysis of ITS 1 gene of Leishmania tropica and evaluation of a novel ligand, benzo[d][1,3]dioxol-5-yl 4-acetamidobenzenesulfonate, via molecular modeling methods

## TL;DR

This study explores a new compound that may inhibit a protein in Leishmania tropica, offering a potential treatment for leishmaniasis.

## Contribution

A novel ligand was synthesized and evaluated as a potential inhibitor of a Leishmania tropica protein using molecular modeling.

## Key findings

- The ligand showed moderate binding affinity and formed multiple hydrogen bonds with the target protein.
- The compound exhibited sustained binding during a 300-ns simulation and reduced protein fluctuation.
- Pharmacological and ADMET analyses support the ligand's potential as a therapeutic agent.

## Abstract

Leishmaniasis, a prevalent tropical disease caused by intracellular protozoa of the genus Leishmania, poses significant health challenges globally, exacerbated by migration waves from endemic regions. Despite its widespread impact, an effective vaccine for leishmaniasis remains elusive. Historically, antimony compounds have been employed in its treatment, but the emergence of resistant strains necessitates the development of new therapeutic agents. Addressing this need, our study focused on the structural characterization of a previously uncharacterized protein from Leishmania tropica using computational biomolecular techniques.

We identified and docked the ligand benzo[d][1,3]dioxol-5-yl 4-acetamidobenzenesulfonate (3) and synthesized the reaction of sesamol (1) with sulfonyl chloride (2), and the NMR and IR spectra were used for characterization, a potential inhibitor of this protein, followed by a 300-ns simulation using the GROMACS software.

The results showed that the protein structure in the ITS1 gene region of L. tropica consisting of 875 amino acids was effectively inhibited. In addition, based on the broad pharmacological properties of sesamol and sulfonate esters, as well as the results obtained from ProTox-III analysis, compound 3 was synthesized and its effect on L. tropica was investigated. This evaluation was further supported by DataWarrior, SwissADME, and ADMETlab analyses. The ligand’s moderate binding affinity (ΔG = −6.29 kcal/mol), the formation of multiple hydrogen bonds (n = 4), its sustained binding throughout the 300-ns simulation, and the observed decrease in root mean square fluctuation (RMSF) values collectively support the idea that the synthesized compound may act as a potential inhibitor.

However, experimental studies are required to conclusively confirm its inhibitory efficacy. This study provides valuable insights for the development of new therapeutic approaches against leishmaniasis.