This study reveals strong anti-ulcer properties of phytocompounds, suggesting effective alternatives to standard treatments for peptic ulcer disease.
Key Points
Musa sapientum phytocompounds showed strong anti-ulcer potential, indicating a viable alternative to proton pump inhibitors.
Epicatechin and Gallocatechin demonstrated binding affinities surpassing Lansoprazole and Omeprazole in molecular docking studies.
Analysis highlighted that most active compounds fulfilled criteria for oral bioavailability, showing promising pharmacokinetic profiles.
Concerns remain for 1,8-Diethoxyanthracene-9,10-dione due to safety risks, while other compounds exhibited favorable drug-likeness and minimal toxicity.