Rare casbane diterpenoids from Hainan soft coral Sinularia depressa. (Articolo in rivista)

Type
Label
  • Rare casbane diterpenoids from Hainan soft coral Sinularia depressa. (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/np900484k (literal)
Alternative label
  • Li Y.; Carbone M.; Vitale R.M.; Amodeo P.; Castelluccio F.; Sicilia G.; Mollo E.; Nappo M.; Cimino G.; Guo Y.-W.; Gavagnin M. (2010)
    Rare casbane diterpenoids from Hainan soft coral Sinularia depressa.
    in Journal of natural products (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Li Y.; Carbone M.; Vitale R.M.; Amodeo P.; Castelluccio F.; Sicilia G.; Mollo E.; Nappo M.; Cimino G.; Guo Y.-W.; Gavagnin M. (literal)
Pagina inizio
  • 133 (literal)
Pagina fine
  • 138 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 73 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 2 (literal)
Note
  • ISI Web of Science (WOS) (literal)
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, People's Republic of China; Istituto di Chimica Biomolecolare (ICB), CNR, Via Campi Flegrei 34, 80078 Pozzuoli, Naples, Italy. (literal)
Titolo
  • Rare casbane diterpenoids from Hainan soft coral Sinularia depressa. (literal)
Abstract
  • A series of nine casbane diterpenes, compounds 5-13, exhibiting either cis or trans ring junctions were isolated from the Hainan soft coral Sinularia depressa. The structures of this group of compounds, the basic member of which was named depressin (5), were established by detailed spectroscopic analysis. In addition, the absolute configuration of the main metabolite, 10-hydroxydepressin (7), and of its epimer, 1-epi-10-hydroxydepressin (8), was determined by a combination of conformational analysis and the modified Mosher's method. A stereochemical relationship between all isolated molecules was investigated by analyzing their circular dichroism profiles. Antiproliferative and antibacterial activities of the depressins were also evaluated. (literal)
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