Racys_2010_Bioorg.Med.Chem_18_4775

Reference

Title : Inhibition of prolyl oligopeptidase with a synthetic unnatural dipeptide - Racys_2010_Bioorg.Med.Chem_18_4775
Author(s) : Racys DT , Rea D , Fulop V , Wills M
Ref : Bioorganic & Medicinal Chemistry , 18 :4775 , 2010
Abstract :

A new inhibitor, containing a linked proline-piperidine structure, for the enzyme prolyl oligopeptidase (POP) has been synthesised and demonstrated to bind covalently with the enzyme at the active site. This provides evidence that covalent inhibitors of POP do not have to be limited to structures containing five-membered N-containing heterocyclic rings.

PubMedSearch : Racys_2010_Bioorg.Med.Chem_18_4775
PubMedID: 20627594
Gene_locus related to this paper: pig-ppce

Related information

Inhibitor Z-Pro-Prolinal-derived
Gene_locus pig-ppce
Structure 2XDW

Citations formats

Racys DT, Rea D, Fulop V, Wills M (2010)
Inhibition of prolyl oligopeptidase with a synthetic unnatural dipeptide
Bioorganic & Medicinal Chemistry 18 :4775

Racys DT, Rea D, Fulop V, Wills M (2010)
Bioorganic & Medicinal Chemistry 18 :4775