Publication | Open Access

Potent and selective P2–P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1′, P1, and/or P3 substitutions

Molecular PharmacologyPharmaceutical ChemistryGood Pharmacokinetic PropertiesBiochemistryMedicineFavorable P1′PharmacotherapyPharmacologyCathepsin KDrug Discovery