Research Article
Elucidating the Mechanisms of Hugan Buzure Granule in the Treatment of Liver Fibrosis via Network Pharmacology
Table 3
Docking results of the top 5 hub targets with active compounds.
| No. | Compound | Affinity (kJ·mol−1) | IL6 | CASP3 | EGFR | VEGF | MAPK |
| 1 | Dl-3n-butylphthalide | −5.4 | −5.2 | −6.4 | −5.3 | −8.5 | 2 | Esculetin | −6.0 | −5.1 | −7.2 | −5.3 | −6.7 | 3 | Apigenin | −6.4 | −6.4 | −8.2 | −6.8 | −9.0 | 4 | Luteolin | −6.6 | −6.8 | −8.4 | −7.1 | −8.9 | 5 | Luteolin-7-o-glucoside | −7.5 | −7.6 | −10.0 | −7.2 | −9.2 | 6 | Poriferast-5-en-3beta-ol | −5.5 | −6.7 | −8.2 | −5.7 | −7.7 | 7 | Beta-sitosterol | −5.7 | −6.4 | −9.1 | −5.8 | −7.7 | 8 | Delphinidin | −6.6 | −6.6 | −8.7 | −7.4 | −8.5 | 9 | Eseramine | −7.1 | −6.5 | −7.6 | −6.1 | −8.1 | 10 | 2S, 2’S-aurantiamide acetate | −6.6 | −7.0 | −9.0 | −6.2 | −7.8 | 11 | Lactucopicrin | −6.0 | −8.0 | −9.2 | −6.3 | −7.9 | 12 | (2R)-3-[3-(5-allyl-2-hydroxyphenyl)-4-hydroxyphenyl]propane-1, 2-diol | −6.2 | −6.6 | −8.0 | −6.0 | −8.1 | 13 | Gitoxigenin | −6.2 | −6.8 | −8.5 | −6.0 | −7.2 | 14 | Cyanidin 3-glucoside | −6.4 | −6.1 | −8.5 | −7.3 | −8.6 | 15 | Ammidin | −6.0 | −6.1 | −8.2 | −6.7 | −8.0 | 16 | Stigmasterol | −6.2 | −6.6 | −8.5 | −6.9 | −8.0 | 17 | Sesamin | −7.2 | −7.3 | −9.7 | −7.1 | −9.5 | 18 | NSC63551 | −6.4 | −7.2 | −9.3 | −5.9 | −8.3 | 19 | Isorhamnetin | −6.5 | −6.7 | −8.3 | −6.8 | −8.8 | 20 | Kaempferol | −6.4 | −6.4 | −8.0 | −6.7 | −8.8 | 21 | Campest-5-en-3beta-ol | −6.1 | −6.1 | −9.1 | −5.5 | −7.5 | 22 | Isofucosterol | −5.8 | −6.5 | −9.5 | −5.8 | −7.9 | 23 | Matrine | −5.7 | −6.0 | −6.7 | −5.5 | −7.4 | 24 | CLR | −5.3 | −6.3 | −7.8 | −5.8 | −7.3 | 25 | Quercetin | −6.5 | −6.8 | −8.5 | −7.2 | −8.5 |
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