Indobufen

CAS No. 63610-08-2

Indobufen ( Ibustrin )

Catalog No. M26717 CAS No. 63610-08-2

Indobufen is an inhibitor of platelet aggregation and is a reversible platelet cyclooxygenase (Cox) activity inhibitor. Indobufen suppresses thromboxane A2 (TxA2) synthesis. Indobufen down-regulates tissue factor (TF) in monocytes.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 36 In Stock
10MG 51 In Stock
25MG 85 In Stock
50MG 124 In Stock
100MG 178 In Stock
200MG 267 In Stock
500MG 461 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Indobufen
  • Note
    Research use only, not for human use.
  • Brief Description
    Indobufen is an inhibitor of platelet aggregation and is a reversible platelet cyclooxygenase (Cox) activity inhibitor. Indobufen suppresses thromboxane A2 (TxA2) synthesis. Indobufen down-regulates tissue factor (TF) in monocytes.
  • Description
    Indobufen is an inhibitor of platelet aggregation and is a reversible platelet cyclooxygenase (Cox) activity inhibitor. Indobufen suppresses thromboxane A2 (TxA2) synthesis. Indobufen down-regulates tissue factor (TF) in monocytes.(In Vitro):Indobufen suppresses TxA2 but not PGE2 synthesis in LPS-stimulated monocytes. Indobufen causes the extent of ERK1/2 phosphorylation, whereas the levels of phosphorylated p38 are unaltered. Indobufen does not affect both Cox-1 and Cox-2 protein, whereas Indobufen reduces TxB2 levels.
  • Synonyms
    Ibustrin
  • Pathway
    Chromatin/Epigenetic
  • Target
    COX
  • Recptor
    RSV
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    63610-08-2
  • Formula Weight
    295.3
  • Molecular Formula
    C18H17NO3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CCC(C(O)=O)c1ccc(cc1)N1Cc2ccccc2C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Lundin A, et al. Two novel fusion inhibitors of human respiratory syncytial virus. Antiviral Res. 2010 Dec;88(3):317-24.
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