VUF 11207 fumarate
- Product Name
- VUF 11207 fumarate
- CAS No.
- 1785665-61-3
- Chemical Name
- VUF 11207 fumarate
- Synonyms
- VUF 11207 fumarate;VUF11207 fumarate, 10 mM in DMSO;N-(3-(2-Fluorophenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide but-2-enedioate;N-[(2E)-3-(2-Fluorophenyl)-2-methyl-2-propen-1-yl]-3,4,5-trimethoxy-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]benzamide fumarate;VUF11207,Inhibitor,CXCR,TnF?α,osteoclast precursor cells,VUF-11207,LPS,CXC chemokine receptors,inhibit,osteoclastogenesis,VUF-11207 fumarate,VUF11207 fumarate,bone resorption,VUF 11207,RANKL
- CBNumber
- CB63311721
- Molecular Formula
- C31H39FN2O8
- Formula Weight
- 586.66
- MOL File
- 1785665-61-3.mol
VUF 11207 fumarate Property
- storage temp.
- Store at -20°C
- solubility
- <58.66mg/ml in Water; <58.66mg/ml in DMSO
- form
- Solid
- color
- Light yellow to yellow
N-Bromosuccinimide Price
- Product number
- 4780
- Product name
- VUF11207fumarate
- Purity
- ≥98%(HPLC)
- Packaging
- 10
- Price
- $231
- Updated
- 2021/12/16
- Product number
- 4780
- Product name
- VUF11207fumarate
- Purity
- ≥98%(HPLC)
- Packaging
- 50
- Price
- $971
- Updated
- 2021/12/16
- Product number
- 257078
- Product name
- VUF 11207 fumarate
- Packaging
- 10mg
- Price
- $489
- Updated
- 2021/12/16
- Product number
- CS-0033233
- Product name
- VUF11207(fumarate)
- Purity
- 98.50%
- Packaging
- 50mg
- Price
- $600
- Updated
- 2021/12/16
- Product number
- CS-0033233
- Product name
- VUF11207(fumarate)
- Purity
- 98.50%
- Packaging
- 100mg
- Price
- $1000
- Updated
- 2021/12/16
VUF 11207 fumarate Chemical Properties,Usage,Production
Uses
VUF11207 fumarate is a CXCR7 agonist that binds specifically to CXCR7. VUF11207 fumarate reduces CXCL12-mediated osteoclastogenesis and bone resorption by inhibiting ERK phosphorylation[1].
in vivo
VUF11207 fumarate (100 μg/day; s.c.; single daily for 5 days) inhibits LPS?induced osteoclastogenesis, bone resorption and production of RANKL and TNF?α in mice[1].
| Animal Model: | Male c57Bl/6J wild?type/WT mice (8?10?week?old; 20?25 g; LPS-induced)[1] |
| 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. |
IC 50
CXCR7: 8.1 (pKi)
storage
Store at -20°C
References
[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. DOI:10.1016/j.ejmech.2012.02.041
[2] Nugraha AP, et al. C?X?C receptor 7 agonist acts as a C?X?C motif chemokine ligand 12 inhibitor to ameliorate osteoclastogenesis and bone resorption. Mol Med Rep. 2022 Mar;25(3):78. DOI:10.3892/mmr.2022.12594
VUF 11207 fumarate Preparation Products And Raw materials
Raw materials
Preparation Products
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