Research Article
Identification of Active Compounds of Mahuang Fuzi Xixin Decoction and Their Mechanisms of Action by LC-MS/MS and Network Pharmacology
Table 2
ADME profile of the compounds from MFXD.
| Compounds | Caco-2 | HIA | F20 | F30 |
| Gallic acid | −5.767 | 0.431 | 0.673 | 0.616 | Cathine | −4.783 | 0.877 | 0.851 | 0.869 | Ephedrine | −4.956 | 0.902 | 0.853 | 0.879 | Higenamine | −5.293 | 0.538 | 0.226 | 0.386 | Pseudoephedrine | −4.956 | 0.902 | 0.853 | 0.879 | Methylephedrine | −4.477 | 0.809 | 0.701 | 0.707 | Vicenin-2 | −6.624 | 0.226 | 0.447 | 0.253 | Catechin | −6.495 | 0.400 | 0.488 | 0.404 | Kaempferitrin | −6.364 | 0.399 | 0.584 | 0.325 | Vitexin | −6.317 | 0.263 | 0.494 | 0.287 | p-Coumaric acid | −4.892 | 0.745 | 0.699 | 0.536 | Quercitrin | −6.469 | 0.155 | 0.515 | 0.242 | Naringenin chalcone | −5.198 | 0.472 | 0.596 | 0.519 | Umbelliferone | −4.601 | 0.797 | 0.534 | 0.441 | Benzoylmesaconine | −6.087 | 0.301 | 0.332 | 0.41 | Germacrone | −4.378 | 0.768 | 0.661 | 0.625 | Coumarin | −4.142 | 0.848 | 0.288 | 0.257 | Ferulic acid | −4.943 | 0.635 | 0.680 | 0.509 | Hypaconitine | −5.513 | 0.343 | 0.265 | 0.350 | Deoxyaconitine | −5.469 | 0.349 | 0.261 | 0.355 | Atractylenolide II | −4.35 | 0.866 | 0.564 | 0.549 | Nardosinone | −4.353 | 0.826 | 0.633 | 0.585 | β-Asarone | −4.379 | 0.763 | 0.722 | 0.681 | Linolenic acid | −4.729 | 0.805 | 0.568 | 0.396 |
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