Skip to main navigation menu Skip to main content Skip to site footer

Virtual screening of inhibitory compounds SEP-2 Candida albicans

Tamizaje virtual de compuestos inhibidores de la SAP-2 de Candida albicans.




Section
Artículos de Investigación

How to Cite
Rebollo, J., Reyes, N., & Suárez, P. (2015). Virtual screening of inhibitory compounds SEP-2 Candida albicans. Archivos De Medicina , 15(2), 260-265. https://doi.org/10.30554/archmed.15.2.675.2015
Download Citation

Dimensions
PlumX

How to Cite

Rebollo, J., Reyes, N., & Suárez, P. (2015). Virtual screening of inhibitory compounds SEP-2 Candida albicans. Archivos De Medicina , 15(2), 260-265. https://doi.org/10.30554/archmed.15.2.675.2015

Download Citation

Juan Rebollo
Niradiz Reyes
Paola Suárez

Juan Rebollo,

Grupo de Micología. Docente Sección de Microbiología. Facultad de Medicina. Universidad de Cartagea

Most read articles by the same author(s)

Objetive: reports of Antifungal resistance to Candida spp. are increasing nowadays. Candida spp. is an opportunistic yeast associated to many different mucocutaneous and systemic diseases. Because of this problematic is necessary to search others new selective and specific compounds against this fungi. Virtual docking is a good alternative to study new molecules. Materials and Methods: here we analyse 13418 compounds
similar to recognized inhibitors of SAP-2, the enzyme selected as antifungal target. SYBYL 8 was the program used to do the docking virtual besides Autodock Vina to finally select the compounds with best scores. Results: similar compounds to protease inhibitors, amprenavir, indinavir, ritonavir shows best scores in virtual docking. Conclusion: the results suggest that similar compounds to protease inhibitors, amprenavir, indinavir and ritonavir could be proposed as model to research new molecules with antifungal activity against Candida spp.

Article visits 422 | PDF visits 306


Downloads

Download data is not yet available.
Sistema OJS 3.4.0.10 - Metabiblioteca |