Design, Synthesis, and Optimization of Novel Epoxide Incorporating Peptidomimetics as Selective Calpain Inhibitors

• Published in: Journal of medicinal chemistry Vol. 56; no. 15; pp. 6054 - 6068
• Main Authors: Schiefer, Isaac T, Tapadar, Subhasish, Litosh, Vladislav, Siklos, Marton, Scism, Rob, Wijewickrama, Gihani T, Chandrasena, Esala P, Sinha, Vaishali, Tavassoli, Ehsan, Brunsteiner, Michael, Fa’, Mauro, Arancio, Ottavio, Petukhov, Pavel, Thatcher, Gregory R. J
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 08-08-2013
• Subjects: Calpain - antagonists & inhibitors; Calpain - chemistry; Catalytic Domain; Click Chemistry; Computer Simulation; Drug Design; Epoxy Compounds - chemical synthesis; Epoxy Compounds - chemistry; Kinetics; Leucine - analogs & derivatives; Leucine - chemical synthesis; Leucine - chemistry; Molecular Docking Simulation; Papain - antagonists & inhibitors; Peptidomimetics - chemical synthesis; Peptidomimetics - chemistry; Stereoisomerism; Structure-Activity Relationship
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm4006719

Hyperactivation of the calcium-dependent cysteine protease calpain 1 (Cal1) is implicated as a primary or secondary pathological event in a wide range of illnesses and in neurodegenerative states, including Alzheimer’s disease (AD). E-64 is an epoxide-containing natural product identified as a potent nonselective, calpain inhibitor, with demonstrated efficacy in animal models of AD. By use of E-64 as a lead, three successive generations of calpain inhibitors were developed using computationally assisted design to increase selectivity for Cal1. First generation analogues were potent inhibitors, effecting covalent modification of recombinant Cal1 catalytic domain (Cal1cat), demonstrated using LC–MS/MS. Refinement yielded second generation inhibitors with improved selectivity. Further library expansion and ligand refinement gave three Cal1 inhibitors, one of which was designed as an activity-based protein profiling probe. These were determined to be irreversible and selective inhibitors by kinetics studies comparing full length Cal1 with the general cysteine protease papain.