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L006235

Cat. No. M10280

All AbMole products are for research use only, cannot be used for human consumption.

L006235 Structure
Synonym:

L235; L-006235; L-235

Size Price Availability Quantity
10mM*1mL in DMSO USD 110  USD110 In stock
5mg USD 110  USD110 In stock
10mg USD 170  USD170 In stock
50mg USD 460  USD460 In stock
100mg USD 680  USD680 In stock
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Quality Control & Documentation
Biological Activity

L006235 (L235) is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays > 4000-fold selectivity over cathepsins B, L and S. L-006235 inhibits bone resorption in the rabbit bone resorption assay, with an IC50 of 5 nM. 

In vivo, L-006235 (0.6-15 mg/kg; p.o.) qd for 8-11 days reduces N-telopeptides (NTx) and creatinine (Cre) by up to 76% dose-dependently in rhesus monkey.

Chemical Information
Molecular Weight 466.6
Formula C24H30N6O2S
CAS Number 294623-49-7
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Lilian N Nwosu, et al. Pain Rep. Analgesic effects of the cathepsin K inhibitor L-006235 in the monosodium iodoacetate model of osteoarthritis pain

[2] Brenda L Pennypacker, et al. J Bone Miner Res. Cathepsin K inhibitors prevent bone loss in estrogen-deficient rabbits

[3] Jean-Pierre Falgueyret, et al. J Med Chem. Lysosomotropism of basic cathepsin K inhibitors contributes to increased cellular potencies against off-target cathepsins and reduced functional selectivity

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CAA-0225 is a tissue protease L inhibitor that inhibits rat liver tissue protease L with a IC50 value of 1.9 nM.

Z-Gly-Pro-Arg-AMC hydrochloride

Z-Gly-Pro-Arg-AMC hydrochloride a fluorescent trypsin and cathepsin K substrate.

N-CBZ-Phe-Arg-AMC

N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes.

Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2

Ac-Glu-Asp(EDANS)-Lys-Pro-Ile-Leu-Phe-Phe-Arg-Leu-Gly-Lys(DABCYL)-Glu-NH2 is a cathepsin D substrate, that can be used for cathepsin D FRET assay.

(S, S)-Z-FA-FMK

(S,S)-Z-FA-FMK is a cell-permeable, irreversible cathepsin B inhibitor.

  Catalog
Abmole Inhibitor Catalog




Keywords: L006235, L235; L-006235; L-235 supplier, Cathepsin, inhibitors, activators

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