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Iso-petromyroxols: novel dihydroxylated tetrahydrofuran enantiomers from sea lamprey (Petromyzon marinus).
Li, Ke; Brant, Cory O; Bussy, Ugo; Pinnamaneni, Harshita; Patel, Hinal; Hoye, Thomas R; Li, Weiming.
Afiliação
  • Li K; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. like4@msu.edu.
  • Brant CO; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. brant@msu.edu.
  • Bussy U; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. bussy@msu.edu.
  • Pinnamaneni H; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. pinnama3@msu.edu.
  • Patel H; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. pinnama3@msu.edu.
  • Hoye TR; Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, MN 55455, USA. hoye@umn.edu.
  • Li W; Department of Fisheries and Wildlife, Michigan State University, East Lansing, MI 48824, USA. liweim@msu.edu.
Molecules ; 20(3): 5215-22, 2015 Mar 23.
Article em En | MEDLINE | ID: mdl-25806547
ABSTRACT
An enantiomeric pair of new fatty acid-derived hydroxylated tetrahydrofurans, here named iso-petromyroxols, were isolated from sea lamprey larvae-conditioned water. The relative configuration of iso-petromyroxol was elucidated with 1D and 2D NMR spectroscopic analyses. The ratio of enantiomers (er) in the natural sample was measured by chiral-HPLC-MS/MS to be ca. 31 of (-)- to (+)-antipodes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Petromyzon / Ácidos Graxos / Furanos Limite: Animals Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Petromyzon / Ácidos Graxos / Furanos Limite: Animals Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos