VUF11207 fumarate

CAS No. 1785665-61-3

VUF11207 fumarate( —— )

Catalog No. M23800 CAS No. 1785665-61-3

VUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 93 In Stock
2MG 48 In Stock
5MG 76 In Stock
10MG 132 In Stock
25MG 273 In Stock
50MG 462 In Stock
100MG 666 In Stock
200MG 926 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    VUF11207 fumarate
  • Note
    Research use only, not for human use.
  • Brief Description
    VUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).
  • Description
    VUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).
  • In Vitro
    Cell Viability Assay Cell Line:Osteoclast precursor cells (RANKL? and TnF?α?induced) Concentration:0.17 nM (100 ng/mL)Incubation Time:5 days Result:Showed inhibitory effect on CXCL12.
  • In Vivo
    Animal Model:Male c57Bl/6J wild?type/WT mice (8?10?week?old; 20?25 g; LPS-induced)Dosage:100 μg/day Administration:Subcutaneous injection; single daily for 5 days Result:Significantly decreased the number of osteoclasts and suppressed Cathepsin K mRNA, ranKl and TnF?α mRNA expression levels.Reduced the area of LPS-induced bone resorption.
  • Synonyms
    ——
  • Pathway
    Autophagy
  • Target
    CXCR
  • Recptor
    CXCR7
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1785665-61-3
  • Formula Weight
    586.65
  • Molecular Formula
    C31H39FN2O8
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:247 mg/mL (421.03 mM; Need ultrasonic)
  • SMILES
    C/C(CN(CCC1N(C)CCC1)C(C2=CC(OC)=C(OC)C(OC)=C2)=O)=C\C3=C(F)C=CC=C3.OC(/C=C/C(O)=O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Wijtmans M, et al. Synthesis, modeling and functional activity of substituted styrene-amides as small-molecule CXCR7 agonists. Eur J Med Chem. 2012 May;51:184-92.
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