Synthesis and antimicrobial activities of His(2-aryl)-Arg and Trp-His(2-aryl) classes of dipeptidomimetics

Synthesis and antimicrobial activities of His(2-aryl)-Arg and Trp-His(2-aryl) classes of dipeptidomimetics Discovery of Trp-His and His-Arg Analogues as New Structural Classes of Short Antimicrobial Peptides Discovery of Short Peptides Exhibiting High Potency against Cryptococcus neoformans Synthetically modified l-histidine-rich peptidomimetics exhibit potent activity against Cryptococcus neoformans Discovery of a Membrane-Active, Ring-Modified Histidine Containing Ultrashort Amphiphilic Peptide That Exhibits Potent Inhibition of Cryptococcus neoformans Modified histidine containing amphipathic ultrashort antifungal peptide, His[2-p-(n-butyl)phenyl]-Trp-Arg-OMe exhibits potent anticryptococcal activity Non hemolytic short peptidomimetics as a new class of potent and broad-spectrum antimicrobial agents Synthesis and bioactivities of new N-terminal dipeptide mimetics with aromatic amide moiety: Broad-spectrum antibacterial activity and high antineoplastic activity Antibacterial evaluation of structurally amphipathic, membrane active small cationic peptidomimetics: Synthesized by incorporating 3-amino benzoic acid as peptidomimetic element Design and synthesis of short amphiphilic cationic peptidomimetics based on biphenyl backbone as antibacterial agents