Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors
2006
We report a novel series of noncovalent inhibitors of cathepsin S. The synthesis of the peptidomimetic scaffold is described and structure–activity relationships of P3, P1, and P1′ subunits are discussed. Lead optimization to a non-peptidic scaffold has resulted in a new class of potent, highly selective, and orally bioavailable cathepsin S inhibitors.
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