产品名称 | AZD 8797 - CX3CR1 antagonist 18a |
产品货号 | Axon 2255 CAS [911715-90-7] MF C19H25N5OS2MW 403.56 Purity: 99% Optical purity: Optically pure Soluble in DMSO Description Potent and selective antagonist of the Fractalkine receptor (FKN or CX3CR1; Ki value 3.9 nM) with a 720 fold selectivity over the CXCR2 receptor, a 246-fold selectivity versus hCCR1 and 187-fold versus hCCR2 and no significant antagonism of the CCR4, CCR5, CCR6, CXCR3, and CXCR5 receptors. AZD 8797 displayed adequate metabolic stability and solubility and high Caco-2 permeability. Notably, AZD 8797 exhibited a significant interaction (>50% activity at 10 μM) for the adenosine A1 receptor only, and the selectivity was later determined to be 33-fold. KEYWORDS: |
产品价格 | 现货询价,电话:010-67529703 |
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产品品牌 | axonmedchem |
产品概述 | |
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AZD 8797 - CX3CR1 antagonist 18aAxon 2255 CAS [911715-90-7] MF C19H25N5OS2
DescriptionPotent and selective antagonist of the Fractalkine receptor (FKN or CX3CR1; Ki value 3.9 nM) with a 720 fold selectivity over the CXCR2 receptor, a 246-fold selectivity versus hCCR1 and 187-fold versus hCCR2 and no significant antagonism of the CCR4, CCR5, CCR6, CXCR3, and CXCR5 receptors. KEYWORDS: AZD 8797 | supplier | CX3CR1 antagonist | CX3CR1 antagonist 18a | AZD8797 | CAS [911715-90-7] | Chemokine | Fractalkine | GPCR | FKN | CX3CR | Caco-2 permeability | migration | adhesion | extravasation | inflammatory | lymphocytes | leukocytes | multiple sclerosis
Potent and selective antagonist of the Fractalkine receptor (FKN or CX3CR1)
Chemical name(R)-2-(2-amino-5-((S)-1-phenylethylthio)thiazolo[4,5-d]pyrimidin-7-ylamino)-4-methylpentan-1-ol Parent CAS No.[911715-90-7] |
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