Generic placeholder image

Current Topics in Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1568-0266
ISSN (Online): 1873-4294

Macrocyclic Inhibitors of HCV NS3-4A Protease: Design and Structure Activity Relationship

Author(s): Srikanth Venkatraman and F. George Njoroge

Volume 7, Issue 13, 2007

Page: [1290 - 1301] Pages: 12

DOI: 10.2174/156802607781212202

Price: $65

Abstract

HCV NS3, a serine protease, that when bound to NS-4A cofactor facilitates development of mature virons by catalyzing cleavage of a single polyprotein to form functional and structural proteins of HCV. X-ray structure of the enzyme reveal a very shallow binding pocket at the catalytic site which makes development of inhibitors a daunting task. Various novel approaches have been used to design, preorganized, depeptidized macrocyclic inhibitors linking the P2-P4 residues and P1-P3 groups. The design and structure activity relationship of these macrocyclic inhibitors are reviewed in the following article. X-ray structure of inhibitor bound to the active site of the enzyme is also discussed. Macrocyclization proved to be an effective tool for depeptidization of peptidic inhibitors, imparting enhanced metabolic stability and improved pharmacokinetic properties in the resultant molecules.

Keywords: Macrocyclization, HCV, NS3 protease, BILN-2061, depeptidization


Rights & Permissions Print Export Cite as
© 2024 Bentham Science Publishers | Privacy Policy