<strong>An approach toward the identification of new antileishmaniasic compounds.</strong>

Abstract

Herein we present results of a quantitative structure-activity relationship (QSAR) study to identify new antileishmaniasic compounds (Leishmania amazonensis) by using a set of more than 2000 0D-2D Dragon´s molecular descriptors and machine learning techniques. A data set of organic chemicals, with antileishmaniasic activity against promastigote forms of the parasite, is used to develop four QSAR models based on k-nearest neighbors, Support Vector Machine, Multi-Layer Perceptron and classification tree techniques. External validation procedures were developed to demonstrate the predictive power of the models. Promastigote´s models correctly classify more than 89% chemicals in both training and external prediction groups, respectively. In addition to the individual techniques an assembled system of majority vote was personalized with the aim of improving the results of the obtained models. To identify new compounds with potential activity against this parasite, a virtual screening was performed using DrugBank international database. There were identified more than five hundred new potential antileishmaniasic compounds. The current results constitute a step forward in the search for efficient ways to discover new antileishmaniasic lead compounds.