GSK805

CAS No. 1426802-50-7

GSK805( —— )

Catalog No. M20717 CAS No. 1426802-50-7

GSK805 is a potent orally bioavailable retinoid-related orphan receptor gamma t (RORγt) inverse agonist that interacts with the receptor's putative ligand binding domain without exerting significant effects on DNA binding.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 139 In Stock
2MG 68 In Stock
5MG 117 In Stock
10MG 187 In Stock
25MG 377 In Stock
50MG 452 In Stock
100MG 648 In Stock
200MG 927 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GSK805
  • Note
    Research use only, not for human use.
  • Brief Description
    GSK805 is a potent orally bioavailable retinoid-related orphan receptor gamma t (RORγt) inverse agonist that interacts with the receptor's putative ligand binding domain without exerting significant effects on DNA binding.
  • Description
    GSK805 is a potent orally bioavailable retinoid-related orphan receptor gamma t (RORγt) inverse agonist that interacts with the receptor's putative ligand binding domain without exerting significant effects on DNA binding.
  • In Vitro
    Cell Differentiation Assay Cell Line:CD4+ T cells Concentration:0.5 μM Incubation Time:4 days Result:Inhibited IL-17 production during Th17 cell differentiation.
  • In Vivo
    GSK805 (10 mg/kg; p.o. once per day for 35 days) improves the situation of mice with experimental autoimmune encephalomyelitis (EAE).GSK805 (30 mg/kg; p.o. once) inhibits Th17 cell responses in EAE mice. Animal Model:C57BL/6 mice were immunized with MOG35–55 plus CFA Dosage:10 mg/kg Administration:Oral gavage; 10 mg/kg once per day; for 35 days Result:Efficiently ameliorated the severity of EAE in mice.Animal Model:C57BL/6 mice with EAE Dosage:30 mg/kg Administration:Oral gavage; 30 mg/kg once Result:Reduced both IFN-γ-IL-17+ and IFN-γ+IL-17+ T cells without altered the frequency of TNF-α+ T cells in EAE mice.
  • Synonyms
    ——
  • Pathway
    Nuclear Receptor/Transcription Factor
  • Target
    ROR
  • Recptor
    RORγt
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1426802-50-7
  • Formula Weight
    532.36
  • Molecular Formula
    C23H18Cl2F3NO4S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:100 mg/mL (187.84 mM)
  • SMILES
    CCS(=O)(=O)c1ccc(CC(=O)Nc2cc(Cl)c(c(Cl)c2)-c2ccccc2OC(F)(F)F)cc1
  • Chemical Name
    N-[26-dichloro-2'-(trifluoromethoxy)[11'-biphenyl]-4-yl]-4-(ethylsulfonyl)-benzeneacetamide

Shipping & Storage Information

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

Reference

1.Xiao S Yosef N Yang J et al. Small-Molecule RORγt Antagonists Inhibit T Helper 17 Cell Transcriptional Network by Divergent Mechanisms[J]. Immunity 2014 40(4):477-489.
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