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. 2023 Dec 9;61(1):1512–1524. doi: 10.1080/13880209.2023.2287658

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© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

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Figure 4. — Molecular docking results of the main chemical components of ZXP. (A–E) Quercetin - ALB; Quercetin - AKT1; Quercetin - INS; Quercetin - TNF; Quercetin - IL-6; (F–J) Kaempferol - ALB; Kaempferol - AKT1; Kaempferol - INS; Kaempferol - TNF; Kaempferol - IL-6; (K–O) licochalcone A - ALB; licochalcone A - AKT1; licochalcone A - INS; licochalcone A - TNF; licochalcone A - IL-6; (P–T) Naringenin - ALB; Naringenin - AKT1; Naringenin - INS; Naringenin - TNF; Naringenin - IL-6;(U–Y) 6,7-dimethoxy-2-(2-phenylethyl) chromone - ALB; 6,7-dimethoxy-2-(2-phenylethyl) chromone - AKT1; 6,7-dimethoxy-2-(2-phenylethyl) chromone - INS; 6,7-dimethoxy-2-(2-phenylethyl) chromone - TNF; 6,7-dimethoxy-2-(2-phenylethyl) chromone - IL-6. The potent highest combination of molecular docking was highlighted with a red border.