Chemical Name:N-(2-Bromophenyl)-N'-(7-cyano-1H-benzotriazol-4-yl)urea
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Potent CXCR2 antagonist that inhibits CINC-1-mediated but not C5a-mediated Ca2+ mobilization (IC50 values are 3.4 and 6800 nM respectively). Inhibits CINC-induced chemotaxis and attenuates neutrophil accumulation in inflammatory lung injury in vivo.
Licensing Information
Sold for research purposes under agreement from GlaxoSmithKline
Technical Data
M. Wt
357.16
Formula
C14H9BrN6O
Storage
Store at RT
Purity
≥98% (HPLC)
CAS Number
211096-49-0
PubChem ID
9841667
InChI Key
SEDUMQWZEOMXSO-UHFFFAOYSA-N
Smiles
O=C(NC3=C(Br)C=CC=C3)NC1=CC=C(C#N)C2=C1NN=N2
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
35.72
100
ethanol
3.57
10
Preparing Stock Solutions
The following data is based on the product molecular weight 357.16. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
2.8 mL
14 mL
28 mL
5 mM
0.56 mL
2.8 mL
5.6 mL
10 mM
0.28 mL
1.4 mL
2.8 mL
50 mM
0.06 mL
0.28 mL
0.56 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
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References
References are publications that support the products' biological activity.
Autenet al (2001) Nonpeptide CXCR2 antagonist prevents neutrophil accumulation in hyperoxia-exposed newborn rats. J.Pharmacol.Exp.Ther. 299 90 PMID: 11561067
Milatovicet al (2003) Impaired healing of nitrogen mustard wounds in CXCR2 null mice. Wound Repair Regen. 11 213 PMID: 12753603