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Purity:99%
Biological Activity |
Potent and selective CXCR2 chemokine receptor antagonist (IC 50 = 22 nM) that displays > 150-fold selectivity over CXCR1 receptors. Causes inhibition of IL-8 and GRO α -mediated calcium mobilization in HL60 cells (IC 50 values are 8 and 10 nM respectively). Prevents IL-8-induced neutrophil chemotaxis in vitro and sequestration in vivo . Inhibits HIV replication in lymphocytes and macrophages. |
Biochem/physiol Actions |
SB-225002 is a potent nonpeptide inhibitor of chemokine receptor CXCR2 with an IC50 of 22 nM for inhibiting interleukin IL-8 binding to CXCR2 and > 150-fold selectivity over CXCR1 receptors. CXCR2 binds many different immune cell chemoattractants. SB-225002 is crucial for cancer progression and is involved in inflammatory diseases like COPD, rheumatoid arthritis, and ulcerative colitis. |
InChI:InChI=1/C13H10BrN3O4/c14-9-3-1-2-4-10(9)15-13(19)16-11-6-5-8(17(20)21)7-12(11)18/h1-7,18H,(H2,15,16,19)
Amyloid β (Aβ), a key molecule in the pa...
The present invention relates to novel c...
This invention relates to the novel use ...
This invention relates to novel compound...
2-bromophenyl isocyanate
5-Nitro-2-aminophenol
1-(2-bromophenyl)-3-(2-hydroxy-4-nitrophenyl)urea
N-(2-hydroxy-4-nitrophenyl)-N'-(2-bromophenylourea
Conditions | Yield |
---|---|
|
47% |
2-bromophenyl isocyanate
5-Nitro-2-aminophenol
1-(2-bromophenyl)-3-(2-hydroxy-4-nitrophenyl)urea
Conditions | Yield |
---|---|
In
tetrahydrofuran;
at 50 ℃;
for 12h;
Inert atmosphere;
|
34% |
|
2-bromophenyl isocyanate
5-Nitro-2-aminophenol
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