STRUCTURE ELUCIDATION OF AUSTRALIFUNGIN, A POTENT INHIBITOR OF SPHINGANINE N-ACYLTRANSFERASE IN SPHINGOLIPID BIOSYNTHESIS FROM SPORORMIELLA-AUSTRALIS

Citation
Od. Hensens et al., STRUCTURE ELUCIDATION OF AUSTRALIFUNGIN, A POTENT INHIBITOR OF SPHINGANINE N-ACYLTRANSFERASE IN SPHINGOLIPID BIOSYNTHESIS FROM SPORORMIELLA-AUSTRALIS, Journal of organic chemistry, 60(6), 1995, pp. 1772-1776
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
60
Issue
6
Year of publication
1995
Pages
1772 - 1776
Database
ISI
SICI code
0022-3263(1995)60:6<1772:SEOAAP>2.0.ZU;2-H
Abstract
The structure elucidation of the novel, potent sphinganine N-acyltrans ferase inhibitor, australifungin (1), from Sporormiella australis is d escribed. Extensive exchange-broadening phenomena predominantly of the keto-enol type were observed on the NMR time scale which was resolved by derivatization to triacetate (2) and tetraacetate (3) derivatives. Residual exchange broadening in the acetates was attributed to hinder ed rotation about the C3-C11 single bond which was frozen out into two conformers at low temperature, The application of 2D NMR techniques t o the structure elucidation of the acetate derivatives at ambient and low temperature therefore contributed considerably to the overall stru cture determination of 1. The conformation and complete relative stere ochemistry followed from a consideration of the Karplus relationship f or H-1-H-1 vicinal coupling constants and phase-sensitive NOE data. Te mperature-dependent NMR experiments suggest an averaged conformational mixture of four to five forms in solution at ambient temperature wher eas a predominant conformer 1 is indicated at low temperature with the enolized beta-keto aldehyde stabilized through internal H-bonding in the cis-orientation. The triacetate 2 and tetraacetate 3, by contrast, are enolized in the sterically favored trans configuration. The beta- keto alcohol derivative australifunginol (6) is also present.