Publication | Open Access
N-Acylated and <scp>d</scp> Enantiomer Derivatives of a Nonamer Core Peptide of Lactoferricin B Showing Improved Antimicrobial Activity
102
Citations
15
References
1999
Year
Bioorganic ChemistryPeptide SciencePeptide TherapeuticsPeptide ChemistryAntimicrobial ChemotherapyPotent PeptideDrug ResistanceMedicinal ChemistryPeptide DerivativesLactoferricin BAntimicrobial ResistanceAntimicrobial Drug DiscoveryAntibacterial AgentAntimicrobial CompoundNon-peptide LigandPharmacologyNonamer Core PeptideNatural SciencesPeptide TherapeuticPeptide SynthesisMicrobiologyMedicineDrug Discovery
N-acylated or D enantiomer peptide derivatives based on the sequence RRWQWRMKK in lactoferricin B demonstrated antimicrobial activities greater than those of lactoferricin B against bacteria and fungi. The most potent peptide, conjugated with an 11-carbon-chain acyl group, showed two to eight times lower MIC than lactoferricin B.
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