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. 2024 Nov 15;15(11):2220–2236. doi: 10.4239/wjd.v15.i11.2220

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©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.

This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.

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Docking poses and interaction pattern of selected targets. A: Fibronectin; B: Interaction with fibronectin; C: Interleukin-6 (IL-6); D: Interaction with IL-6; E: Tumor necrosis factor-α (TNF-α); F: Interaction with TNF-α; G: Interleukin-1β (IL-1β); H: Interaction with IL-1β; I: Transforming growth factor-beta 1 (TGF-β1); J: Interaction with TGF-β1. The docking pose of targets selected based on the binding affinity and RMSD ≤ 3.0 Å interacted with Tiliroside. TGF-β1: Transforming growth factor-beta 1; TNF-α: Tumor necrosis factor-α; IL-6: Interleukin-6; IL-1β: Interleukin-1β.