Secondly, the analysis of compound–compound target network and the PPI network of compound targets displayed that PIK3CG, CASP3, BCL2, CASP8, and MMP1 might be the key targets of the YCHD associated with hepatitis C. Thirdly, it can be seen by molecular docking that the active ingredient in the YCHD has strong binding activity to two potential targets and has good binding activity to most potential targets. This evidence concerns the gene MMP1 and hepatitis C virus infection.