SX-576
SX-576 is a CXCR1 and CXCR2 antagonist with IC50 values of 31 nM and 21 nM, respectively. SX-576 inhibits neutrophil infiltration in a rat model of pulmonary inflammation. SX-576 can be used in studies related to pulmonary inflammation.
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- CAS No.: 1240494-14-7
- 화학식: C20H15BF4N2O4S
- 분자량:466.21
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
SX-576 inhibits GROα-mediated intracellular calcium release in isolated human polymorphonuclear leukocytes (PMNs) with an IC50 of 22 ± 3 nM[1].
SX-576 acts as a full antagonist in CXCR2-expressing cells in the PathHunter β-arrestin assay with an IC50 of 130 ± 6 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley rats[1]
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Dosage:1 mg/kg
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Administration:i.v.; three doses (at t=0, t=5, t=9 hours)
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Result:Significantly decreased neutrophil influx to the lungs to near undetectable levels.
Significantly reduced macrophage influx.
Significantly reduced ozone-induced lung leakage, as measured by reduced BALF protein levels.
Chemical Information
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CAS No. 1240494-14-7
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분자량 466.21
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화학식 C20H15BF4N2O4S
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SMILES
O=C(NC1=CC=C(F)C=C1)C2=CN=C(SCC3=CC(OC(F)(F)F)=CC=C3B(O)O)C=C2
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)