Biel_2006_Chemistry_12_4121

Reference

Title : Synthesis and evaluation of acyl protein thioesterase 1 (APT1) inhibitors - Biel_2006_Chemistry_12_4121
Author(s) : Biel M , Deck P , Giannis A , Waldmann H
Ref : Chemistry , 12 :4121 , 2006
Abstract :

Lipid-modified proteins play decisive roles in important biological processes such as signal transduction, organisation of the cytoskeleton and vesicular transport. Lipidation of these proteins is essential for correct biological function. Among the modifications with lipids, prenylation and myristoylation are well understood. However, the machinery of palmitoylation is still under investigation. Recently, an enzyme, acyl protein thioesterase 1 (APT1), that may play a regulatory role in the palmitoylation cycle of H-Ras and G-protein alpha subunits, was purified. Motivated by this work, several inhibitors of APT1 were designed, synthesized and biologically evaluated leading to highly active compounds.

PubMedSearch : Biel_2006_Chemistry_12_4121
PubMedID: 16528788

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Citations formats

Biel M, Deck P, Giannis A, Waldmann H (2006)
Synthesis and evaluation of acyl protein thioesterase 1 (APT1) inhibitors
Chemistry 12 :4121

Biel M, Deck P, Giannis A, Waldmann H (2006)
Chemistry 12 :4121