| Autor: |
Ke Li, Brant, Cory O., Bussy, Ugo, Pinnamaneni, Harshita, Patel, Hinal, Hoye, Thomas R., Weiming Li |
| Předmět: |
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| Zdroj: |
Molecules; Mar2015, Vol. 20 Issue 3, p5215-5222, 8p, 2 Diagrams, 1 Chart, 2 Graphs |
| Abstrakt: |
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. 3:1 of (-)- to (+)-antipodes. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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