L006235 is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that exhibits > 4000-fold selectivity over cathepsins B, L and S. References: Soung do Y, Gentile MA, Duong le T, Drissi H. Effects of pharmacological inhibition of cathepsin K on fracture repair in mice. Bone. 2013 Jul;55(1):248-55. doi: 10.1016/j.bone.2013.02.010. Epub 2013 Feb 26. PubMed PMID: 23486186.

纯度：≥98%

CAS：294623-49-7