HIF2α-IN-2

CAS No. 1422955-31-4

HIF2α-IN-2( TCS 7009 | TC S 7009 | TC-S 7009 )

Catalog No. M11779 CAS No. 1422955-31-4

HIF2α-IN-2 is a potent, selective, allosteric inhibitor of HIF-2α PAS-B domain with Kd of 81 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 67 In Stock
5MG 61 In Stock
10MG 116 In Stock
25MG 235 In Stock
50MG 342 In Stock
100MG 505 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    HIF2α-IN-2
  • Note
    Research use only, not for human use.
  • Brief Description
    HIF2α-IN-2 is a potent, selective, allosteric inhibitor of HIF-2α PAS-B domain with Kd of 81 nM.
  • Description
    HIF2α-IN-2 is a potent, selective, allosteric inhibitor of HIF-2α PAS-B domain with Kd of 81 nM, shows high selectivity and does not affect HIF-1 function; antagonizes HIF-2 heterodimerization and DNA-binding activity in vitro and in cultured cells, reducing HIF-2 target gene expression.
  • In Vitro
    Cell Proliferation Assay Cell Line:HPF cells in hypoxic conditions Concentration:0-100?μM Incubation Time:72 hours Result:Showed greater inhibition of cell proliferation in hypoxic conditions than that in normoxic conditions.
  • In Vivo
    ——
  • Synonyms
    TCS 7009 | TC S 7009 | TC-S 7009
  • Pathway
    Angiogenesis
  • Target
    HIF/HIF Prolyl-hydroxylase
  • Recptor
    HIF/HIF Prolyl-hydroxylase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1422955-31-4
  • Formula Weight
    308.653
  • Molecular Formula
    C12H6ClFN4O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (162.00 mM)
  • SMILES
    O=[N+](C1=C(NC2=CC(F)=CC(Cl)=C2)C=CC3=NON=C31)[O-]
  • Chemical Name
    N-(3-chloro-5-fluorophenyl)-4-nitrobenzo[c][1,2,5]oxadiazol-5-amine

Shipping & Storage Information

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

Reference

1. Scheuermann TH, et al. Nat Chem Biol. 2013 Apr;9(4):271-6.
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