产品详情 |
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Product Name | L 006235 |
Description | Potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays > 4000-fold selectivity over cathepsins B, L and S. Displays reduced selectivity in cell-based assays possibly due to lysosomal accumulation. Reduces collagen breakdown and promotes bone deposition in vivo. Orally active and has intrinsic fluorescence. Purity 98%. MW (observed): 466.6 |
Size | 10 mg |
Concentration | n/a |
Applications | n/a |
Other Names | N-[1-[[(Cyanomethyl)amino]carbonyl]cyclohexyl]-4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]benzamide |
Gene, Accession, CAS # | CAS: 294623-49-7 |
Catalog # | 3066/10 |
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Order / More Info | L 006235 from TOCRIS BIOSCIENCE
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Product Specific References | n/a |
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