Novel Peptide–Triazole Conjugates: Strategic Synthesis, Antimicrobial Properties, and Molecular Docking Study
The rising incidence of multidrug‐resistant (MDR) bacteria demands the creation of innovative antimicrobial agents characterized by enhanced stability and efficacy. In this study, a series of peptide–heterocycle conjugates was systematically designed and synthesized using solid‐phase peptide synthesis (SPPS), featuring...