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 |
| 2MG | 45 | In Stock |
|
| 5MG | 72 | In Stock |
|
| 10MG | 125 | In Stock |
|
| 25MG | 258 | In Stock |
|
| 50MG | 447 | In Stock |
|
| 100MG | 644 | In Stock |
|
| 200MG | 896 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameVUF11207 fumarate
-
NoteResearch use only, not for human use.
-
Brief DescriptionVUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).
-
DescriptionVUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).
-
In VitroCell 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 VivoAnimal 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——
-
PathwayAutophagy
-
TargetCXCR
-
RecptorCXCR7
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1785665-61-3
-
Formula Weight586.65
-
Molecular FormulaC31H39FN2O8
-
Purity>98% (HPLC)
-
SolubilityDMSO:247 mg/mL (421.03 mM; Need ultrasonic)
-
SMILESC/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℃)
-
ShippingWith 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.
molnova catalog
related products
-
Reparixin L-lysine s...
Reparixin L-lysine salt is an allosteric chemokine receptor 1/2 (CXCR1/2) activation inhibitor.
-
AMD 3465 hexahydrobr...
AMD 3465 hexahydrobromide is a CXCR4 receptor antagonist with potential anticancer and anti-HIV activity.
-
Syringaresinol-di-O-...
1. Syringaresinol-di-O-glucoside protects the animals from the stress-induced decreases in sex behaviours and in rectal temperature, the stress-induced failure of retrieval of memory, and the stress-induced enlargement of adrenal gland.
Cart
sales@molnova.com