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Danirixin
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Danirixin图片
CAS NO:954126-98-8
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 441.90
Formula C19H21ClFN3O4S
CAS No. 954126-98-8
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 8 mg/mL (18.10 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Chemical Name (S)-1-(4-chloro-2-hydroxy-3-(piperidin-3-ylsulfonyl)phenyl)-3-(3-fluoro-2-methylphenyl)urea
Synonyms GSK1325756; GSK-1325756; GSK 1325756
实验参考方法
In Vitro

In vitro activity: Danirixin (formerly known as GSK1325756) is a a potent small molecule CXCR2 antagonist being developed as a potential anti-inflammatory drug. It is a selective, high-affinity and reversible CXCR2 antagonist with IC50 of 12.5 nM for CXCL8. The dose-dependent inhibition of agonist-induced neutrophil activation following single and repeated once daily oral administration of danirixin suggests that this CXCR2 antagonist may have benefit in neutrophil-predominant inflammatory diseases. Excessive neutrophil presence and activation is important in a number of acute and chronic inflammatory diseases. The CXCR2 chemokine receptor is important in controlling the extravasation and activation of neutrophils. Selective antagonism of the CXCR2 receptor is a potential approach to reducing neutrophil migration and activation.


Kinase Assay: It is a selective, high-affinity and reversible CXCR2 antagonist with IC50 of 12.5 nM for CXCL8.


Cell Assay:

In Vivo
Animal model
Formulation & Dosage
References BMC Pharmacol Toxicol. 2015 Jun 20;16:18.