R406 free base

CAS No. 841290-80-0

R406 free base( —— )

Catalog No. M16126 CAS No. 841290-80-0

R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 58 In Stock
10MG 88 In Stock
25MG 177 In Stock
50MG 320 In Stock
100MG 507 In Stock
500MG 1062 In Stock
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Biological Information

  • Product Name
    R406 free base
  • Note
    Research use only, not for human use.
  • Brief Description
    R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay.
  • Description
    R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. Phase 1.
  • In Vitro
    R406 inhibits adenosine A3 receptor (IC50=0.081 μM), adenosine transporter (IC50=1.84 μM), and monoamine transporter (IC50=2.74 μM).R406 inhibits Huh7 hepatocyte, A549 epithelial, and H1299 lung cancer lines with EC50s of 15.1, 2.9 and 6.3 μM, respectively.R406 inhibits phosphorylation of Syk substrate LAT in mast cells and BLNK/SLP65 in B cells. Western Blot Analysis Cell Line:Cultured human mast cells (CHMC Concentration:0.016, 0.08, 0.4, 2 μM Incubation Time:40 minutes Result:Inhibited all other kinases tested at 5 to 100 fold less potency than Syk as judged by phosphorylation of target proteins.
  • In Vivo
    R406 (5 and 10 mg/kg) shows efficacy in the amelioration of the Arthus reaction and in reducing clinical symptoms in the collagen antibody-induced arthritis (CAIA) and K/BxN models of rheumatoid arthritis (RA). Immune complex (IC)-mediated inflammation is reduced by inhibition of Fc receptor signaling with R406. Animal Model:Female Balb/c mice (6-8 weeks) with CAIA Dosage:5 and 10 mg/kg Administration:Administered orally, b.i.d, for 14 days, starting 4 hours after antibody challenge on day 0. Result:Reduced inflammation and swelling, and the arthritis progressed more slowly in treated animals than in vehicle controls.Animal Model:Female C57BL/6 mice with arthritis Dosage:10 mg/kg Administration:Administered orally one hour before serum injection; b.i.d; for 13 days Result:Delayed the onset and reduced the severity of clinical arthritis. Paw thickening and clinical arthritis were reduced by approximately 50%.
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    Syk
  • Recptor
    Syk
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    841290-80-0
  • Formula Weight
    470.45
  • Molecular Formula
    C22H23FN6O5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 21 mg/mL (44.63 mM)
  • SMILES
    COC1=CC(NC2=NC=C(F)C(NC3=NC4=C(OC(C)(C)C(=O)N4)C=C3)=N2)=CC(OC)=C1OC
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Braselmann S, et al. J Pharmacol Exp Ther, 2006, 319(3), 998-1008.
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