Structure-activity relationship studies of putaminoxins and pinolidoxins: Phytotoxic nonenolides produced by phytopathogenic Phoma and Ascochyta species (Articolo in rivista)

Type
Label
  • Structure-activity relationship studies of putaminoxins and pinolidoxins: Phytotoxic nonenolides produced by phytopathogenic Phoma and Ascochyta species (Articolo in rivista) (literal)
Anno
  • 1998-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/(SICI)1522-7189(199809/10)6:5<183::AID-NT23>3.0.CO;2-U (literal)
Alternative label
  • Evidente, Antonio; Capasso, Renato; Andolfi, Anna; Vurro, Maurizio; Zonno, Maria Chiara (1998)
    Structure-activity relationship studies of putaminoxins and pinolidoxins: Phytotoxic nonenolides produced by phytopathogenic Phoma and Ascochyta species
    in Natural toxins (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Evidente, Antonio; Capasso, Renato; Andolfi, Anna; Vurro, Maurizio; Zonno, Maria Chiara (literal)
Pagina inizio
  • 183 (literal)
Pagina fine
  • 188 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/record/display.url?eid=2-s2.0-0032451103&origin=inward (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 6 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 5 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Universita degli Studi di Napoli Federico II (literal)
Titolo
  • Structure-activity relationship studies of putaminoxins and pinolidoxins: Phytotoxic nonenolides produced by phytopathogenic Phoma and Ascochyta species (literal)
Abstract
  • Putaminoxin and pinolidoxin, two structurally related nonenolides, isolated respectively from organic extracts of Phoma putaminum and Aschochyta pinodes cultures, together with some of their natural analogs and synthetic derivatives, were used in a structure-activity relationship study. Their phytotoxic, antifungal and zootoxic activities were assayed with the aim to find compounds with potential herbicidal properties. The strongest phytotoxic compounds proved to be putaminoxin and pinolidoxin, whose activity appeared to be correlated to the integrity of the nonenolide ring and to the presence of both the hydroxy groups and the unmodified propyl side chain. None of the assayed nonenolides showed antifungal activity, whereas pinolidoxin analogs and derivatives showed high to weak zootoxicity. (literal)
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