Multievaluation Strategy for Liujunzi Decoction: Fingerprint Characterization, Chemometrics Analysis, Network Pharmacology, and Molecular Docking

Table 1

Molecular docking results of some components with targets.

Target name	Ingredient	Binding energy (kJ/mol)
SRC	Ephedrine hydrochloride	−5.4
	Hesperidin	−9.5
	Ginsenoside RG1	−7.8
	Jujuboside A	−8.6
MAPK1	Ephedrine hydrochloride	−5.4
	Hesperidin	−8.6
	Ginsenoside RG1	−7.2
	Jujuboside A	−9.5
PIK3R1	Ephedrine hydrochloride	−5
	Hesperidin	−7.8
	Ginsenoside RG1	−7.5
	Jujuboside A	−8.4
AKT1	Ephedrine hydrochloride	−5.5
	Hesperidin	−8.6
	Ginsenoside RG1	−8
	Jujuboside A	−8.6

Note. When the ligand binds to the receptor, the more stable the conformation is, the lower the energy is, and the greater the possibility of interaction is. The binding energy ≤−5 kJ/mol is used to judge the interaction ability.