2-Cyano-pyrimidines: a new chemotype for inhibitors of the cysteine protease cathepsin K.

ABSTRACT

Starting from the purine lead structure 1, a new series of cathepsin K inhibitors based on a pyrimidine scaffold have been explored. Investigations of P3 and P2 substituents based on molecular modeling suggestions resulted in potent cathepsin K inhibitors with an improved selectivity profile over other cathepsins.