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| | GSK-CXCR2 Basic information |
| Product Name: | GSK-CXCR2 | | Synonyms: | GSK-CXCR2;N-(2-Bromophenyl)-N'-(7-cyano-1H-benzotriazol-4-yl)urea;SB 265610;1-(2-Bromophenyl)-3-(4-cyano-1H-benzo[d] [1,2,3]triazol-7-yl)urea;Urea, N-(2-bromophenyl)-N'-(4-cyano-1H-benzotriazol-7-yl)-;SB265610 >=98% (HPLC);CXCR,nonpeptide,inhibit,Inhibitor,SB-265610,inflammation,recruitment,Delay,SB 265610,healing,neutrophil,SB265610,wound,CXC chemokine receptors | | CAS: | 211096-49-0 | | MF: | C14H9BrN6O | | MW: | 357.16 | | EINECS: | | | Product Categories: | | | Mol File: | 211096-49-0.mol |  |
| | GSK-CXCR2 Chemical Properties |
| Boiling point | 527.0±45.0 °C(Predicted) | | density | 1.77±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | DMSO: soluble15mg/mL, clear | | pka | 6.13±0.40(Predicted) | | form | powder | | color | white to light brown |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 |
| | GSK-CXCR2 Usage And Synthesis |
| Uses | SB 265610 is an anti-tumor pharmaceutical developed to act as an antagonist to cysteine-amino acid-cysteine (CXC) chemokines receptor 2 antagonist. | | Biological Activity | Potent CXCR2 antagonist that inhibits CINC-1-mediated but not C5a-mediated Ca 2+ mobilization (IC 50 values are 3.4 and 6800 nM respectively). Inhibits CINC-induced chemotaxis and attenuates neutrophil accumulation in inflammatory lung injury in vivo . | | Biochem/physiol Actions | SB265610 is a potent and selective CXCR2 chemokine receptor antagonist. It has a Kd = 2.5 nM. | | storage | Store at RT |
| | GSK-CXCR2 Preparation Products And Raw materials |
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