Schnurri-3 inhibitor-1

CAS No. 736154-60-2

Schnurri-3 inhibitor-1( —— )

Catalog No. M35439 CAS No. 736154-60-2

Schnurri-3 inhibitor-1, a potent inhibitor of schnurri-3, is an essential regulator of bone formation in adults that can be used in osteoporosis research. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in osteoblast cell line Shn3FFL (AC50 = 2.09 μM) .

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
50MG 38 Get Quote
100MG 63 Get Quote
200MG 88 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Schnurri-3 inhibitor-1
  • Note
    Research use only, not for human use.
  • Brief Description
    Schnurri-3 inhibitor-1, a potent inhibitor of schnurri-3, is an essential regulator of bone formation in adults that can be used in osteoporosis research. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in osteoblast cell line Shn3FFL (AC50 = 2.09 μM) .
  • Description
    Schnurri-3 inhibitor-1 is a potent schnurri-3 inhibitor which is an essential regulator of adult bone formation. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in osteoblast cell line Shn3FFL with an AC50 value of 2.09 μM. Schnurri-3 inhibitor-1 can be used to research osteoporosis.
  • In Vitro
    Schnurri-3 inhibitor-1 (0-50 μM; 24 h) can inhibit Shn3 with EF1alpha promoter in SV40 large T antigen-transformed osteoblast cell line (Clone20-Shn3FFL) with an AC50 value of 2.09 μM.Schnurri-3 inhibitor-1 (0.195-26 μM; 48 h) exhibits moderate activity in HepG2 mammalian cells with an AC50 value of 54.73 μM.ell Viability Assay Cell Line:Clone20-Shn3FFL cells Concentration:2.09 μM Incubation Time:24 hours Result:Showed the active concentration AC50 value of 2.09 μM.Cell Viability Assay Cell Line:Clone20-Shn3FFL cells Concentration:1.2 μM Incubation Time:24 hours Result:Showed the active concentration AC50 value of 1.2 μM.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    736154-60-2
  • Formula Weight
    284.28
  • Molecular Formula
    C12H10F2N2O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (879.41 mM; Ultrasonic )
  • SMILES
    Fc1ccc(cc1F)S(=O)(=O)NCc1ccncc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. National Center for Biotechnology Information. PubChem Compound Summary for CID 2473445.
molnova catalog
related products
  • IRAK4-IN-4

    IRAK4-IN-4 inhibits cyclic GMP-AMP synthase (cGAS) with an IC50 of 2.1 nM.IRAK4-IN-4 is an interleukin-1 receptor–associated kinase 4 (IRAK4) inhibitor, has an IC50 of 2.8 nM.

  • GSK2879552 dihydroch...

    GSK2879552 dihydrochloride an orally active, selective and irreversible inhibitor of lysine specific demethylase 1 (LSD1/KDM1A), with potential antineoplastic activity.

  • Dimethyl malonate

    Dimethyl Malonate is a Succinate Dehydrogenase inhibitor.