Virtual screening of inhibitory compounds SEP-2 Candida albicans
Tamizaje virtual de compuestos inhibidores de la SAP-2 de Candida albicans.
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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
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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
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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.
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