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Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.
Tsukamoto, Sachiko; Umaoka, Hideharu; Yoshikawa, Kohei; Ikeda, Tsuyoshi; Hirota, Hiroshi.
Affiliation
  • Tsukamoto S; Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan. sachiko@kumamoto-u.ac.jp
J Nat Prod ; 73(8): 1438-40, 2010 Aug 27.
Article in En | MEDLINE | ID: mdl-20795742
ABSTRACT
Notoamides O-R were isolated from a marine-derived Aspergillus sp. Notoamide O possesses a novel hemiacetal/hemiaminal ether functionality hitherto unknown among this family of prenylated indole alkaloids. The structure represents an unusual branch point for the oxidative modification of other members in the family of prenylated indole alkaloids in the biogenetic pathway.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Indole Alkaloids Limits: Animals Language: En Journal: J Nat Prod Year: 2010 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Indole Alkaloids Limits: Animals Language: En Journal: J Nat Prod Year: 2010 Document type: Article Affiliation country: Japan