FAUC 1104

CAS No. 1869983-86-7

FAUC 1104( FAUC1104 | FAUC-1104 )

Catalog No. M12894 CAS No. 1869983-86-7

A potent, biased allosteric agonist of CXCR3 (pEC50=5.22) that activates solely G proteins.

Purity : >98% (HPLC)

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

Biological Information

  • Product Name
    FAUC 1104
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, biased allosteric agonist of CXCR3 (pEC50=5.22) that activates solely G proteins.
  • Description
    A potent, biased allosteric agonist of CXCR3 (pEC50=5.22) that activates solely G proteins, induces chemotaxis, but fails to induce receptor internalization or β-arrestin 2 recruitment.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    FAUC1104 | FAUC-1104
  • Pathway
    GPCR/G Protein
  • Target
    Chemokine Receptor
  • Recptor
    Chemokine Receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1869983-86-7
  • Formula Weight
    774.959
  • Molecular Formula
    C46H54N4O7
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    tert-Butyl {(S)-1-[(2,2-diphenylethyl)amino]-6-[(S)-2-(4-(4-methoxyphenyl)-4-oxobutanoyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamido]-1-oxohexan-2-yl}carbamate

Shipping & Storage Information

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

Reference

1. Milanos L, et al. J Med Chem. 2016 Mar 10;59(5):2222-43.
molnova catalog
related products
  • CXCR2-IN-1

    A potent, CNS penetrant CXCR2 antagonist with pIC50 of 9.3; shows neutrophil chemotaxis inhibition with pIC50 of 7.6.

  • AZD 5069

    AZD 5069 (AZD5069)?is a potent, selective, slowly reversible and orally bioavailable CXCR2 antagonist that inhibits CXCL8 binding to CXCR2 with pIC50 of 9.1.

  • E 6130

    A potent, selective, orally available CX3C chemokine receptor 1 (CX3CR1) modulator that inhibits the fractalkine-induced chemotaxis of human peripheral blood NK cells with IC50 of 4.9 nM.