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Chemical diversity in lipopeptide antifungal antibiotics.
- Source :
-
Journal of industrial microbiology & biotechnology [J Ind Microbiol Biotechnol] 2001 Sep; Vol. 27 (3), pp. 157-62. - Publication Year :
- 2001
-
Abstract
- In the course of screening for antifungal antibiotics, we have discovered a novel series of lipopeptide compounds structurally related to, but highly superior to, echinocandin B in terms of their water solubility due to the presence of a sulfate residue. These compounds, WF11899s, WF738s, WF14573s, WF16616 and WF22210, and their derivatives have diversity in their nuclear structures and acyl side chains. The producing strains were classified into two groups, the Coleomycetes group and the Hyphomycetes group. Compound FK463, a derivative of WF11899A, is currently in Phase 3 clinical development as a novel antifungal antibiotic.
- Subjects :
- Animals
Anti-Bacterial Agents metabolism
Anti-Bacterial Agents pharmacology
Anti-Bacterial Agents therapeutic use
Antifungal Agents metabolism
Antifungal Agents pharmacology
Antifungal Agents therapeutic use
Candida albicans drug effects
Candidiasis drug therapy
Candidiasis microbiology
Disease Models, Animal
Echinocandins
Fungi metabolism
Glucosyltransferases antagonists & inhibitors
Humans
Mice
Microbial Sensitivity Tests
Mitosporic Fungi metabolism
Peptides, Cyclic metabolism
Peptides, Cyclic pharmacology
Peptides, Cyclic therapeutic use
Anti-Bacterial Agents chemistry
Antifungal Agents chemistry
Fungal Proteins
Membrane Proteins
Peptides
Peptides, Cyclic chemistry
Schizosaccharomyces pombe Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 1367-5435
- Volume :
- 27
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of industrial microbiology & biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 11780786
- Full Text :
- https://doi.org/10.1038/sj.jim.7000091