Lipstatin, an inhibitor of pancreatic lipase, produced by Streptomyces toxytricini. II. Chemistry and structure elucidation.

Erich Hochuli(Roche (Switzerland)), E. KUPFER(Roche (Switzerland)), Richard I. Maurer(Roche (Switzerland)), Walter Meister(Roche (Switzerland)), Y. MERCADAL(Roche (Switzerland)), K. Schmidt(Roche (Switzerland))
The Journal of Antibiotics
January 1, 1987
Cited by 145Open Access
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Abstract

The structure of a new pancreatic lipase inhibitor, lipstatin, produced by Streptomyces toxytricini was determined as (2S,3S,5S,7Z,10Z)-5-[(S)-2-formamido-4-methylpentanoyloxy ]-2-hexyl-3- hydroxy-7,10-hexadecadienoic lactone by spectroscopic and chemical methods. Structurally lipstatin is closely related to the known esterase inhibitor esterastin. It contains a N-formyl-L-leucine side chain instead of the N-acetyl-L-asparagine in esterastin.


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