dc.contributor | University of Iowa | |
dc.contributor | University of Toronto | |
dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-27T11:21:17Z | |
dc.date.available | 2014-05-27T11:21:17Z | |
dc.date.created | 2014-05-27T11:21:17Z | |
dc.date.issued | 2005-03-01 | |
dc.identifier | Journal of Natural Products, v. 68, n. 3, p. 435-438, 2005. | |
dc.identifier | 0163-3864 | |
dc.identifier | http://hdl.handle.net/11449/68141 | |
dc.identifier | 10.1021/np049592f | |
dc.identifier | 2-s2.0-17444373466 | |
dc.identifier | 0000-0001-7616-9652 | |
dc.description.abstract | 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. | |
dc.language | eng | |
dc.relation | Journal of Natural Products | |
dc.relation | 3.885 | |
dc.relation | 1,368 | |
dc.rights | Acesso restrito | |
dc.source | Scopus | |
dc.subject | cyclopentane derivative | |
dc.subject | furan derivative | |
dc.subject | lactone | |
dc.subject | antifungal agent | |
dc.subject | antiinfective agent | |
dc.subject | communiol A | |
dc.subject | communiol B | |
dc.subject | communiol C | |
dc.subject | communiol D | |
dc.subject | communiol E | |
dc.subject | communiol F | |
dc.subject | communiol G | |
dc.subject | communiol H | |
dc.subject | cyclopentene derivative | |
dc.subject | furanocyclopentane derivative | |
dc.subject | furanocyclopentene derivative | |
dc.subject | gamma lactone derivative | |
dc.subject | natural product | |
dc.subject | polyketide | |
dc.subject | unclassified drug | |
dc.subject | chemical structure | |
dc.subject | chemistry | |
dc.subject | Ecuador | |
dc.subject | isolation and purification | |
dc.subject | mass spectrometry | |
dc.subject | nuclear magnetic resonance | |
dc.subject | Podospora | |
dc.subject | United States | |
dc.subject | antibacterial activity | |
dc.subject | antifungal activity | |
dc.subject | Bacillus subtilis | |
dc.subject | Candida albicans | |
dc.subject | carbon nuclear magnetic resonance | |
dc.subject | drug isolation | |
dc.subject | drug structure | |
dc.subject | fungus culture | |
dc.subject | fungus isolation | |
dc.subject | nonhuman | |
dc.subject | nuclear magnetic resonance spectroscopy | |
dc.subject | nuclear Overhauser effect | |
dc.subject | Podospora communis | |
dc.subject | proton nuclear magnetic resonance | |
dc.subject | Staphylococcus aureus | |
dc.subject | stereochemistry | |
dc.subject | structure analysis | |
dc.subject | California | |
dc.subject | Cyclopentanes | |
dc.subject | Furans | |
dc.subject | Lactones | |
dc.subject | Mass Spectrometry | |
dc.subject | Molecular Structure | |
dc.subject | Nuclear Magnetic Resonance, Biomolecular | |
dc.subject | Coprophilous | |
dc.subject | Fungi | |
dc.title | Communiols E-H: New polyketide metabolites from the coprophilous fungus Podospora communis | |
dc.type | Artículos de revistas | |