Ibudilast

CAS No. 50847-11-5

Ibudilast( AV 411 | KC-404 )

Catalog No. M14741 CAS No. 50847-11-5

Ibudilast(KC-404;AV-411;MN-166) is a relatively nonselective phosphodiesterase inhibitor which has been marketed for treating asthma.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 43 In Stock
10MG 37 In Stock
25MG 46 In Stock
50MG 48 In Stock
100MG 73 In Stock
200MG 94 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Ibudilast
  • Note
    Research use only, not for human use.
  • Brief Description
    Ibudilast(KC-404;AV-411;MN-166) is a relatively nonselective phosphodiesterase inhibitor which has been marketed for treating asthma.
  • Description
    Ibudilast(KC-404;AV-411;MN-166) is a relatively nonselective phosphodiesterase inhibitor which has been marketed for treating asthma.
  • In Vitro
    Western Blot Analysis Cell Line:Microglia Concentration:1~100 μM Incubation Time:24 hours Result:Suppressed both IL-1β and IL-6 production at 100 μM, and significantly suppresses TNF-α production at 10 and 100 μM. ?
  • In Vivo
    ——
  • Synonyms
    AV 411 | KC-404
  • Pathway
    Angiogenesis
  • Target
    PDE
  • Recptor
    PDE
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    50847-11-5
  • Formula Weight
    230.51
  • Molecular Formula
    C14H18N2O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 28 mg/mL; 100 mM in Ethanol
  • SMILES
    CC(C)C(C1=C2C=CC=CN2N=C1C(C)C)=O
  • Chemical Name
    2-methyl-1-(2-propan-2-ylpyrazolo[1,5-a]pyridin-3-yl)propan-1-one

Shipping & Storage Information

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

Reference

1.Yamazaki T, et al. Eur J Pharmacol. 2010 Oct 29.
molnova catalog
related products
  • GSK-256066

    A potent, selective PDE4 inhibitor with pIC50 of 11.5, 11.3, 11.4, and 11.9 for PDE4B, A, C, and D, respectively.

  • SCH-00013

    A novel cardiotonic agent that acts as a calcium sensitizer with no chronotropic activity in mammalian cardiac muscle.

  • AMG-579

    AMG-579 is a potent, selective, CNS penetrant, orally bioavailable PDE10A inhibitor with IC50 of 0.1 nM.