SF-22

CAS No. 824981-55-7

SF-22( —— )

Catalog No. M36383 CAS No. 824981-55-7

SF-22 is a neuropeptide Y receptor (Y2R) antagonist that crosses the blood-brain barrier and has potential anti-inflammatory activity for the study of diseases associated with neurological disorders.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 46 Get Quote
5MG 65 Get Quote
10MG 107 Get Quote
25MG 227 Get Quote
50MG 364 Get Quote
100MG 566 Get Quote
500MG 1161 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    SF-22
  • Note
    Research use only, not for human use.
  • Brief Description
    SF-22 is a neuropeptide Y receptor (Y2R) antagonist that crosses the blood-brain barrier and has potential anti-inflammatory activity for the study of diseases associated with neurological disorders.
  • Description
    SF-22 is a neuropeptide Y receptor (Y2R) antagonist that crosses the blood-brain barrier and has potential anti-inflammatory activity for the study of diseases associated with neurological disorders.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Neuropeptide Y Receptor
  • Recptor
    Neuropeptide Y Receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    824981-55-7
  • Formula Weight
    470.58
  • Molecular Formula
    C28H26N2O3S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC1=CC(NS(=O)(=O)C2=C(C)C=CC(=C2)C(=O)NC2=CC=CC=C2C2=CC=CC=C2)=C(C)C=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • M617

    Selective galanin GAL1 receptor agonist (Ki values are 0.23 and 5.71 nM for GAL1 and GAL2 receptors respectively). Enhances food consumption in rats following i.c.v. administration and reduces CAP-induced inflammatory pain.

  • GR 231118

    Potent neuropeptide Y (NPY) Y1 receptor antagonist (pA2 = 10 and 10.5 at rY1 and hY1, receptors respectively). Also a potent and selective NPY Y4 receptor agonist (pEC50 values are 6.0, 8.6 and 6.1 for rY2, hY4 and rY5 receptors respectively). Suppresses food intake in rats in vivo. Also has affinity for neuropeptide FF (NPFF) receptors in vitro (Ki = 43-73 nM).

  • Pancreatic Polypepti...

    Agonist at Y4 neuropeptide Y receptors.