Abstract
The metabolic fate of 2(RS),3-epiminosqualene (Isq.), a demonstrable inhibitor of the 2,3-oxidosqualene-lanosterol cyclase, has been studied in Gibberella fujikuroi. The fungus transforms Isq. to a tetracyclic product for which the 24(RS),25-epiminolanosterol (EL) formulation was indicated by chromatographic and spectral data. The results are consistent with the pathway: Isq.→2,3-imino-22, 23-oxidosqualene→EL.
Original language | English |
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Pages (from-to) | 375-376 |
Number of pages | 2 |
Journal | Lipids |
Volume | 23 |
Issue number | 4 |
DOIs | |
State | Published - Apr 1988 |