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A novel glucagon-like peptide-1 (GLP-1)/glucagon hybrid peptide with triple-acting agonist activity at glucose-dependent insulinotropic polypeptide, GLP-1, and glucagon receptors and therapeutic potential in high fat-fed mice

launchdate:1747206000

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FIGURE 3 The structure–activity relationship data (presented in Figure 3) encouraged us to carry out in silico studies to screen 43 acefylline compounds for MAO-B inhibition activity by utilizing the molecular fragment hybridization and computer-aided drug design (CADD) approaches such as molecular docking, molecular dynamics (MD) simulation, and density functional theory (DFT)