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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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1240494-14-7
- 分子式: C20H15BF4N2O4S
- 分子量:466.21
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
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.
化学情報
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CAS 番号 1240494-14-7
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分子量 466.21
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分子式 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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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)