Three new polycyclic ethanones, named alternethanoxins C-E, were isolated together with the well-known and closely related alternethanoxins A and B, from the solid culture of Alternaria sonchi, a fungal pathogen proposed for perennial sowthistle (Sonchus arvensis L.) biocontrol. Alternethanoxins C-E were characterized by spectroscopic methods (essentially NMR and HRESI MS) as 2'-dihydroxymethyl-2,5,6,6'-tetrahydroxy-3'-methoxy-biphenyl-3-carboxylic acid methyl ester, 1,4,6,9,10-pentahydroxy-7-methoxy-6H-benzo[c]chromene-2-carboxylic acid methyl ester, and 7,9-dihydroxy-2-methoxy-9H-4,8-dioxa-cyclopenta[def]phenanthrene-5-carboxylic acid methyl ester. When assayed on leaf segments of weeds (Sonchus arvensis and Elytrigia repens), alternethanoxins A and C showed phytotoxic activity inducing notable necrotic lesions. Alternethanoxins C and D possess notable antimicrobial activity when tested against Bacillus subtilis (MIC 10 μg/disc) and Candida tropicalis (MIC 25 μg/disc). Alternethanoxins A and B had low activity against these microbes, while alternethanoxin E was inactive.

Alternethanoxins C–E, Further Polycyclic Ethanones Produced byAlternaria sonchi, a Potential Mycoherbicide forSonchus arvensisBiocontrol / Alexander, Berestetskiy; Cimmino, Alessio; Julia, Sofronova; Anna, Dalinova; Fabiana, Avolio; Evidente, Marco; Leonid, Chisty; Denis, Krivorotov; Evidente, Antonio. - In: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY. - ISSN 0021-8561. - 63:(2015), pp. 1196-1199. [10.1021/jf5054595]

Alternethanoxins C–E, Further Polycyclic Ethanones Produced byAlternaria sonchi, a Potential Mycoherbicide forSonchus arvensisBiocontrol

CIMMINO, ALESSIO
Writing – Review & Editing
;
EVIDENTE, MARCO
Formal Analysis
;
EVIDENTE, ANTONIO
Supervision
2015

Abstract

Three new polycyclic ethanones, named alternethanoxins C-E, were isolated together with the well-known and closely related alternethanoxins A and B, from the solid culture of Alternaria sonchi, a fungal pathogen proposed for perennial sowthistle (Sonchus arvensis L.) biocontrol. Alternethanoxins C-E were characterized by spectroscopic methods (essentially NMR and HRESI MS) as 2'-dihydroxymethyl-2,5,6,6'-tetrahydroxy-3'-methoxy-biphenyl-3-carboxylic acid methyl ester, 1,4,6,9,10-pentahydroxy-7-methoxy-6H-benzo[c]chromene-2-carboxylic acid methyl ester, and 7,9-dihydroxy-2-methoxy-9H-4,8-dioxa-cyclopenta[def]phenanthrene-5-carboxylic acid methyl ester. When assayed on leaf segments of weeds (Sonchus arvensis and Elytrigia repens), alternethanoxins A and C showed phytotoxic activity inducing notable necrotic lesions. Alternethanoxins C and D possess notable antimicrobial activity when tested against Bacillus subtilis (MIC 10 μg/disc) and Candida tropicalis (MIC 25 μg/disc). Alternethanoxins A and B had low activity against these microbes, while alternethanoxin E was inactive.
2015
Alternethanoxins C–E, Further Polycyclic Ethanones Produced byAlternaria sonchi, a Potential Mycoherbicide forSonchus arvensisBiocontrol / Alexander, Berestetskiy; Cimmino, Alessio; Julia, Sofronova; Anna, Dalinova; Fabiana, Avolio; Evidente, Marco; Leonid, Chisty; Denis, Krivorotov; Evidente, Antonio. - In: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY. - ISSN 0021-8561. - 63:(2015), pp. 1196-1199. [10.1021/jf5054595]
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/610708
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 17
  • ???jsp.display-item.citation.isi??? 16
social impact