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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
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MedChemExpress LLC
- CAS号：
887401-92-5
- 规格：
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥716.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥625.0 |
| 规格： | 10 mg | 产品价格： | ￥1000.0 |
| 规格： | 25 mg | 产品价格： | ￥1788.0 |
| 规格： | 50 mg | 产品价格： | ￥2650.0 |
| 规格： | 100 mg | 产品价格： | ￥3938.0 |
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INCB 3284
CAS No. : 887401-92-5
MCE 国际站：INCB 3284
产品活性：INCB 3284 是一种有效的，选择性的人 CCR2 拮抗剂，能够抑制单核细胞趋化蛋白 1 与 hCCR2 结合，IC50 值为 3.7 nM。INCB 3284 可用于急性肝功能衰竭的研究。
研究领域：GPCR/G Protein | Immunology/Inflammation
作用靶点：CCR
In Vitro: INCB 3284 is a pentent, selective and orally bioavailable human CCR2 antagonist, inhibiting monocyte chemoattractant protein-1 binding to hCCR2, with an IC50 of 3.7 nM. INCB 3284 also causes an IC50 of 4.7 nM in antagonism of chemotaxis activity, an IC50 of 84 μM in inhibition of the hERG potassium current. However, INCB 3284 has no effec on CCR1, CCR3, CCR5, CXCR3, and CXCR5, or additional GPCRs at a concentration of 1 μM. Moreover, INCB 3284 potently inhibits CCR2-mediated signaling events such as intracellular calcium mobilization and ERK phosphorylation with IC50 values of 6 and 2.6 nM, respectively.
In Vivo: INCB 3284 (1 mg/kg/day, ip) reduces liver damage, and decreases microglia activation in AOM-treated mice via inhibition on CCR2. INCB 3284 also significantly reduces the pERK1/2 to tERK1/2 ratio, as well as G-protein signaling pathway activity and proinflammatory cytokine production in cortex lysates from mice administed with azoxymethane.
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文献和实验(1.30-5.60)122±0.98125±0.96(120-146)4.87±0.845.06±0.93(3.80-7.95)92.3±1.0496.5±1.19(90.0-115)22.0±4.0020.9±3.80(12.8-30.0)5.33±1.155.30±1.10(3.00-7.63)9.60±0.6310.7±0.58(8.30-12.0)2.35±0.252.46±0.27(1.80-3.00)兔0.32±0.040.30±0.04(0.00-0.74)26.7±12.924.5±
.0 ALT U/L 31.38±9.92 276 12.44-63.60
Chromatographic Analysis of the Escherichia coli Polysialic Acid Capsule
Polysialic acid capsules are the major virulence factors in Escherichia coli K1, K92, and groups B and C meningococci. The sialic acid monomers (2-keto-3-deoxy-5-acetamido-7,8,9-d -glycero -d -galacto -nonulosonic acids) comprising
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