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Z Naturforsch C J Biosci ; 60(7-8): 587-90, 2005.
Article in English | MEDLINE | ID: mdl-16163834

ABSTRACT

The use of conventional and unconventional reaction methodology for the hydrolysis of the acetate group in zaluzanin D resulted in hydration of the 11,13 exocyclic bond along with deacetylation. But the microorganism E. coli selectively cleaved the acetate group to yield zaluzanin C.


Subject(s)
Escherichia coli/metabolism , Sesquiterpenes/pharmacokinetics , Antifungal Agents/pharmacology , Escherichia coli/genetics , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Molecular Structure , Sesquiterpenes/chemistry , Sesquiterpenes/pharmacology , Sesquiterpenes, Guaiane
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