Prenylated flavonoids: Pharmacology and biotechnology (Articolo in rivista)

Type
Label
  • Prenylated flavonoids: Pharmacology and biotechnology (Articolo in rivista) (literal)
Anno
  • 2005-01-01T00:00:00+01:00 (literal)
Alternative label
  • Botta B., Vitali A., Menendez P., Misiti D., Delle Monache G. (2005)
    Prenylated flavonoids: Pharmacology and biotechnology
    in Current medicinal chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Botta B., Vitali A., Menendez P., Misiti D., Delle Monache G. (literal)
Pagina inizio
  • 713 (literal)
Pagina fine
  • 739 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 12 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Botta, Misiti: Università Sapienza di Roma Menendez: Facultas de Quimica, Montevideo, Uruguay (literal)
Titolo
  • Prenylated flavonoids: Pharmacology and biotechnology (literal)
Abstract
  • Within the flavonoid class of natural products the prenylated sub-class is quite rich in structural variety and pharmacological activity. In the last twenty years a huge number of new structures has been reported, mostly from Leguminosae and Moraceae, with few coining from other genera. The presence, in different forms, of the isoprenoid chain can lead to impressive changes in biological activity, mostly attributed to an increased affinity for biological membranes and to an improved interaction with proteins. Molecules, such as xanthohumol and sophoraflavarione G, while being very structurally simple, show numerous pharmacological applications and are ideal candidates for SAR aimed to the discovery of new drugs. (literal)
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