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L-006235

Chemical Structure : L-006235

CAS No.: 294623-49-7

L-006235 (L006235;L 006235;CRA-013783;CRA 013783;L-235)

Catalog No.: PC-60641Not For Human Use, Lab Use Only.

L-006235 (L-235, CRA-013783) is a potent, selective, orally bioavailable cathepsin K inhibitor with IC50 of 0.25 nM, displays >4,000-fold selectivity over cathepsins B, L and S.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

L-006235 (L-235, CRA-013783) is a potent, selective, orally bioavailable cathepsin K inhibitor with IC50 of 0.25 nM, displays >4,000-fold selectivity over cathepsins B, L and S.
L-006235 exhibits an IC50 of 28 nM at cellular level in human osteoclasts, >1,000-fold selectivity against cathepsin S.
L-006235 reduces bone erosion, cartilage degradation and inflammation evoked by collagen-induced arthritis in mice.

Physicochemical Properties

M.Wt 466.6
Formula C24H30N6O2S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

100 mM in DMSO

Chemical Name/SMILES

N-[1-[[(Cyanomethyl)amino]carbonyl]cyclohexyl]-4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]benzamide

References

1. Palmer JT, et al. J Med Chem. 2005 Dec 1;48(24):7520-34.

2. Falgueyret JP, et al. J Med Chem. 2005 Dec 1;48(24):7535-43.

3. Svelander L, et al. Eur J Pharmacol. 2009 Jun 24;613(1-3):155-62.

4. Hayami T, et al. Bone. 2012 Jun;50(6):1250-9.

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