SC-236

CAS No. 170569-86-5

SC-236( SC236 | SC58236 )

Catalog No. M12605 CAS No. 170569-86-5

SC-236 (SC58236) is a potent, selective, orally active inhibitor of COX-2 with IC50 of 10 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 44 In Stock
5MG 39 In Stock
10MG 58 In Stock
25MG 117 In Stock
50MG 206 In Stock
100MG 306 In Stock
200MG 442 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SC-236
  • Note
    Research use only, not for human use.
  • Brief Description
    SC-236 (SC58236) is a potent, selective, orally active inhibitor of COX-2 with IC50 of 10 nM.
  • Description
    SC-236 (SC58236) is a potent, selective, orally active inhibitor of COX-2 with IC50 of 10 nM; displays >1,700-fold selectivity over COX-1 (IC50=17.8 uM); exhibits anti-inflammatory properties and potent antimetastatic activity both in vitro and in vivo.
  • In Vitro
    Western Blot Analysis Cell Line:vECs.Concentration:15 μM Incubation Time:30 min.Result:Showd significant reduction in COX-2 level and increase in IκBα level, thus preventing ALSS-induced NFκB activation and inflammation in vECs.Western Blot Analysis Cell Line:COS 7 cells.Concentration:3 and 10 μM.Incubation Time:18 h (combined with 15d-PGJ2).Result:Acted in a concentration-dependent manner as a PPARγ agonist.
  • In Vivo
    Animal Model:Seventy-six male adult Wistar rats weighing 200-220 g (CCl4-treated).Dosage:6 mg/kg.Administration:Orally, 3 times per week.Result:A marked induction of COX-2 protein expression was detected by immunohistochemistry in the liver of CCl4-treated rats.Significantly reduced the degree of liver fibrosis.Dramatically suppressed α-SMA expression in CCl4-treated rats.
  • Synonyms
    SC236 | SC58236
  • Pathway
    Chromatin/Epigenetic
  • Target
    COX
  • Recptor
    COX
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    170569-86-5
  • Formula Weight
    401.8
  • Molecular Formula
    C16H11ClF3N3O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (248.89 mM)
  • SMILES
    O=S(C1=CC=C(N2N=C(C(F)(F)F)C=C2C3=CC=C(Cl)C=C3)C=C1)(N)=O
  • Chemical Name
    4-[5-(4-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-benzenesulfonamide

Shipping & Storage Information

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

Reference

1. Penning TD, et al. J Med Chem. 1997 Apr 25;40(9):1347-65. 2. Lee A, et al. Cancer Res. 2006 Apr 15;66(8):4378-84. 3. Roche-Nagle G, et al. Br J Cancer. 2004 Jul 19;91(2):359-65.
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