L 006235

CAS No. 294623-49-7

L 006235( —— )

Catalog No. M22746 CAS No. 294623-49-7

L 006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 53 In Stock
5MG 87 In Stock
10MG 147 In Stock
25MG 295 In Stock
50MG 500 In Stock
100MG 718 In Stock
500MG 1485 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    L 006235
  • Note
    Research use only, not for human use.
  • Brief Description
    L 006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.
  • Description
    L 006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.
  • In Vitro
    ——
  • In Vivo
    Animal Model:Rhesus monkey (15 years) receiving oophorectomy (OVX)Dosage:0.6, 3, 15 mg/kg Administration:P.o once daily for 8-11 days Result:Decreased uNTx/Cre by an average of 76%, 68%, and 31% at the dose of 15, 3, and 0.6 mg/kg, respectively.
  • Synonyms
    ——
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Cysteine Protease
  • Recptor
    cathepsin K
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    294623-49-7
  • Formula Weight
    466.6
  • Molecular Formula
    C24H30N6O2S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:42mg/ml
  • SMILES
    CN1CCN(CC1)c1nc(cs1)-c1ccc(cc1)C(=O)NC1(CCCCC1)C(=O)NCC#N
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Lena Svelande , Helena Erlandsson-Harris, Leif Astner, et al.Inhibition of cathepsin K reduces bone erosion, cartilage degradation and inflammation evoked by collagen-induced arthritis in mice.Eur J Pharmacol. 2009 Jun 24;613(1-3):155-62.
molnova catalog
related products
  • Liraglutide

    Liraglutide is a long-acting GLP-1 receptor agonist.

  • Cathepsin X-IN-1

    Cathepsin X-IN-1 (compound 25) is a potent Cathepsin X inhibitor (IC50 = 7.13 μM) that reduces PC-3 cell migration with low cytotoxicity .

  • JTE-607 HCl

    JTE-607 is a cytokine production inhibitor. JTE-607 induces apoptosis accompanied by an increase in p21waf1/cip1 in acute myelogenous leukemia cells.