CAY10471 Racemate

CAS No. 844639-57-2

CAY10471 Racemate( TM30089 Racemate )

Catalog No. M20762 CAS No. 844639-57-2

CAY 10471 is a potent highly selective CRTH2/DP 2 receptor antagonist. CAY10471 binds to the human CRTH2/DP2 DP1 and TP receptors( Ki values of 0.6 1200 and >10000 nMrespectively).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 40 In Stock
5MG 65 In Stock
10MG 102 In Stock
25MG 215 In Stock
50MG 320 In Stock
100MG 474 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CAY10471 Racemate
  • Note
    Research use only, not for human use.
  • Brief Description
    CAY 10471 is a potent highly selective CRTH2/DP 2 receptor antagonist. CAY10471 binds to the human CRTH2/DP2 DP1 and TP receptors( Ki values of 0.6 1200 and >10000 nMrespectively).
  • Description
    CAY 10471 is a potent highly selective CRTH2/DP 2 receptor antagonist. CAY10471 binds to the human CRTH2/DP2 DP1 and TP receptors( Ki values of 0.6 1200 and >10000 nMrespectively).
  • In Vitro
    CAY10471 Racemate (Compound 13) inhibits PGD2-induced inositol phosphate or cAMP formation, suppresses β-arrestin translocation with IC50s of 12 and 3 nM, respectively.
  • In Vivo
    ——
  • Synonyms
    TM30089 Racemate
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    GPR
  • Recptor
    CRTh2 (DP2) receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    844639-57-2
  • Formula Weight
    416.47
  • Molecular Formula
    C21H21FN2O4S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:150 mg/mL (360.17 mM)
  • SMILES
    CN(C1CCc2c(C1)c1ccccc1n2CC(O)=O)S(=O)(=O)c1ccc(F)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ulven T Kostenis E . Minor Structural Modifications Convert the Dual TP/CRTH2 Antagonist Ramatroban into a Highly Selective and Potent CRTH2 Antagonist[J]. Journal of Medicinal Chemistry 2005 48(4):897-900.
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