Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
Computational Identification of Potential Small Molecule Capping Groups
4:03
Synthesis of Potential N-capping Groups
6:25
Solid Phase Synthesis for the Generation of FLIPs
8:45
Results: Identification of More Drug-like Inhibitors of CDK2 through the Cyclin Groove
9:59
Conclusion
We describe implementation of the REPLACE strategy for targeting protein-protein interactions. REPLACE is an iterative strategy involving synthetic and computational approaches for the conversion of optimized peptidic inhibitors into drug like molecules.