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http://acervodigital.unesp.br/handle/11449/68141
- Title:
- Communiols E-H: New polyketide metabolites from the coprophilous fungus Podospora communis
- University of Iowa
- University of Toronto
- Universidade Estadual Paulista (UNESP)
- 0163-3864
- Communiols E-H (1-4), four new polyketide-derived natural products containing furanocyclopentane, furanocyclopentene, cyclopentene, or γ-lactone moieties, have been isolated from two geographically distinct isolates of the coprophilous fungus Podospora communis. The structures of these compounds were determined by analysis of NMR and MS data. © 2005 American Chemical Society and American Society of Pharmacognosy.
- 1-Mar-2005
- Journal of Natural Products, v. 68, n. 3, p. 435-438, 2005.
- 435-438
- cyclopentane derivative
- furan derivative
- lactone
- antifungal agent
- antiinfective agent
- communiol A
- communiol B
- communiol C
- communiol D
- communiol E
- communiol F
- communiol G
- communiol H
- cyclopentene derivative
- furanocyclopentane derivative
- furanocyclopentene derivative
- gamma lactone derivative
- natural product
- polyketide
- unclassified drug
- chemical structure
- chemistry
- Ecuador
- isolation and purification
- mass spectrometry
- nuclear magnetic resonance
- Podospora
- United States
- antibacterial activity
- antifungal activity
- Bacillus subtilis
- Candida albicans
- carbon nuclear magnetic resonance
- drug isolation
- drug structure
- fungus culture
- fungus isolation
- nonhuman
- nuclear magnetic resonance spectroscopy
- nuclear Overhauser effect
- Podospora communis
- proton nuclear magnetic resonance
- Staphylococcus aureus
- stereochemistry
- structure analysis
- California
- Cyclopentanes
- Furans
- Lactones
- Mass Spectrometry
- Molecular Structure
- Nuclear Magnetic Resonance, Biomolecular
- Coprophilous
- Fungi
- http://dx.doi.org/10.1021/np049592f
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/68141
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