Triose Phosphate Isomerase Structure-Based Virtual Screening and In Vitro Biological Activity of Natural Products as <i>Leishmania mexicana</i> Inhibitors

Cutaneous leishmaniasis (CL) is a public health problem affecting more than 98 countries worldwide. No vaccine is available to prevent the disease, and available medical treatments cause serious side effects. Additionally, treatment failure and parasite resistance have made the development of new dr...

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Main Authors: Luis D. González-Morales (Author), Adriana Moreno-Rodríguez (Author), Lenci K. Vázquez-Jiménez (Author), Timoteo Delgado-Maldonado (Author), Alfredo Juárez-Saldivar (Author), Eyra Ortiz-Pérez (Author), Alma D. Paz-Gonzalez (Author), Edgar E. Lara-Ramírez (Author), Lilian Yépez-Mulia (Author), Patricia Meza (Author), Gildardo Rivera (Author)
Format: Book
Published: MDPI AG, 2023-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Luis D. González-Morales  |e author 
700 1 0 |a Adriana Moreno-Rodríguez  |e author 
700 1 0 |a Lenci K. Vázquez-Jiménez  |e author 
700 1 0 |a Timoteo Delgado-Maldonado  |e author 
700 1 0 |a Alfredo Juárez-Saldivar  |e author 
700 1 0 |a Eyra Ortiz-Pérez  |e author 
700 1 0 |a Alma D. Paz-Gonzalez  |e author 
700 1 0 |a Edgar E. Lara-Ramírez  |e author 
700 1 0 |a Lilian Yépez-Mulia  |e author 
700 1 0 |a Patricia Meza  |e author 
700 1 0 |a Gildardo Rivera  |e author 
245 0 0 |a Triose Phosphate Isomerase Structure-Based Virtual Screening and In Vitro Biological Activity of Natural Products as <i>Leishmania mexicana</i> Inhibitors 
260 |b MDPI AG,   |c 2023-07-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15082046 
500 |a 1999-4923 
520 |a Cutaneous leishmaniasis (CL) is a public health problem affecting more than 98 countries worldwide. No vaccine is available to prevent the disease, and available medical treatments cause serious side effects. Additionally, treatment failure and parasite resistance have made the development of new drugs against CL necessary. In this work, a virtual screening of natural products from the BIOFACQUIM and Selleckchem databases was performed using the method of molecular docking at the triosephosphate isomerase (TIM) enzyme interface of <i>Leishmania mexicana</i> (<i>L</i>. <i>mexicana</i>). Finally, the in vitro leishmanicidal activity of selected compounds against two strains of <i>L</i>. <i>mexicana</i>, their cytotoxicity, and selectivity index were determined. The top ten compounds were obtained based on the docking results. Four were selected for further in silico analysis. The ADME-Tox analysis of the selected compounds predicted favorable physicochemical and toxicological properties. Among these four compounds, <b>S-8</b> (IC<sub>50</sub> = 55 µM) demonstrated a two-fold higher activity against the promastigote of both <i>L. mexicana</i> strains than the reference drug glucantime (IC<sub>50</sub> = 133 µM). This finding encourages the screening of natural products as new anti-leishmania agents. 
546 |a EN 
690 |a <i>Leishmania</i> 
690 |a triosephosphate isomerase 
690 |a molecular docking 
690 |a natural products 
690 |a virtual screening 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 8, p 2046 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/8/2046 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/dc3210e9930940d1a45fbb9da827b40b  |z Connect to this object online.