Title : Exploring the pharmacological components and effective mechanism of Mori Folium against periodontitis using network pharmacology and molecular docking.

Pub. Date : 2022 Jul

PMID : 35430443






2 Functional Relationships(s)
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1 Molecular docking revealed that Quercetin, Moracin D, Moracin E, Moracin G, Moracin H and Moracin B were able to bind stably to AKT1, PTGS2 and ESR1 targets, with Moracin E showing the most stable structure after binding to AKT1. Moracin G AKT serine/threonine kinase 1 Homo sapiens
2 Molecular docking revealed that Quercetin, Moracin D, Moracin E, Moracin G, Moracin H and Moracin B were able to bind stably to AKT1, PTGS2 and ESR1 targets, with Moracin E showing the most stable structure after binding to AKT1. Moracin G AKT serine/threonine kinase 1 Homo sapiens