Cerinolactone, a hydroxy-lactone derivative from Trichoderma cerinum (Articolo in rivista)

Type
Label
  • Cerinolactone, a hydroxy-lactone derivative from Trichoderma cerinum (Articolo in rivista) (literal)
Anno
  • 2012-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/np200577t (literal)
Alternative label
  • Vinale, Francesco; Girona, Isabel Arjona; Nigro, Marco; Mazzei, Pierluigi; Piccolo, Alessandro; Ruocco, Michelina; Woo, S. L.; Rosa, David Ruano; Herrera, Carlos Loépez; Lorito, Matteo (2012)
    Cerinolactone, a hydroxy-lactone derivative from Trichoderma cerinum
    in Journal of natural products (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Vinale, Francesco; Girona, Isabel Arjona; Nigro, Marco; Mazzei, Pierluigi; Piccolo, Alessandro; Ruocco, Michelina; Woo, S. L.; Rosa, David Ruano; Herrera, Carlos Loépez; Lorito, Matteo (literal)
Pagina inizio
  • 103 (literal)
Pagina fine
  • 106 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/record/display.url?eid=2-s2.0-84856502836&origin=inward (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 75 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Consiglio Nazionale delle Ricerche; Universita degli Studi di Napoli Federico II; CSIC - Instituto de Agricultura Sostenible (IAS) (literal)
Titolo
  • Cerinolactone, a hydroxy-lactone derivative from Trichoderma cerinum (literal)
Abstract
  • A novel metabolite, 3-hydroxy-5-(6-isopropyl-3-methylene-3,4,4a,5,6,7,8,8a- octahydronaphthalen-2-yl)dihydrofuran-2-one, trivially named cerinolactone (1), has been isolated from culture filtrates of Trichoderma cerinum together with three known butenolides containing the 3,4-dialkylfuran-2(5H)-one nucleus, harzianolide (2), T39butenolide (3), and dehydroharzianolide (4). The structure of 1 was determined by spectroscopic methods, including UV, MS, and 1D and 2D NMR analyses. In vitro tests with the purified compound exhibited activity against Pythium ultimum, Rhizoctonia solani, and Botrytis cinerea. © 2011 The American Chemical Society and American Society of Pharmacognosy. (literal)
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