Abstract:
:By the introduction of various amide surrogates, novel pseudopeptides corresponding to a membrane active depsipeptide were synthesized and their native characteristics compared with that of the peptide. The pseudopeptides had more resistance to serum proteases than the peptide and similar antimicrobial activities to that of the peptide without hemolytic activity. The pseudopeptides like the peptide were active against current drug resistant fungi and pathogenic fungi isolated from patients, and also had a strong synergism with current antifungal drugs against Candida albicans. The leakage assay suggested that the pseudopeptides also acted on the lipid membrane of pathogenic cells. These results indicated that the novel pseudopeptides had advantages over the peptide as a candidate for a novel antifungal drug and backbone modifications can be a tool in the development of a novel antifungal agent from membrane-active peptides isolated from natural sources or chemically synthesized.
journal_name
Bioorg Med Chemjournal_title
Bioorganic & medicinal chemistryauthors
Oh JE,Hong SY,Lee KHdoi
10.1016/s0968-0896(99)00176-5subject
Has Abstractpub_date
1999-11-01 00:00:00pages
2509-15issue
11eissn
0968-0896issn
1464-3391pii
S0968-0896(99)00176-5journal_volume
7pub_type
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