Novel Peptide–Triazole Conjugates: Strategic Synthesis, Antimicrobial Properties, and Molecular Docking Study
A series of peptide–heterocycle conjugates was systematically designed and synthesized using solid‐phase peptide synthesis (SPPS), featuring octapeptide‐triazole conjugates modified with a triazole‐based moiety to create innovative antimicrobial agents characterized by enhanced stability and efficacy.