Synthesis of amino heterocycle aspartyl protease inhibitors. Issue 22 (4th May 2016)

• Record Type: Journal Article
• Authors: Chambers, Rachel K.; Khan, Tanweer A.; Olsen, David B.; Sleebs, Brad E.
• Is Part Of: Organic & biomolecular chemistry. Volume 14:Issue 22(2016)
• Page Start: 4970
• Page End: 4985
• Publication Date: 2016-05-04
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c5ob01842k
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : Synthetic strategies to access 2-amino heterocycle head groups that inhibit aspartyl proteases, are reviewed. Abstract : Aspartyl proteases are important pharmacological targets. Historically aspartyl proteases have been commonly targeted with transition state derived peptidomimetics. The strategy to develop aspartyl protease inhibitors has undertaken a dramatic paradigm shift in the last 10 years. The pharmaceutical industry in 2005 disclosed several scaffolds or "head groups" that prompted the field to move beyond peptidomimetic derived inhibitors. Since the discovery of the first amino heterocycle aspartyl protease inhibitor, the amino hydantoin, industry and academia have positioned themselves for a foothold on the new molecular space, designing a variety of related "head groups". Both the design and synthetic efforts involved in constructing these scaffolds are varied and complex. Here we highlight the synthetic strategies used to access these amino heterocycle scaffolds.