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- 2025年12月05日
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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
- 供应商：
MedChemExpress LLC
- CAS号：
566203-88-1
- 规格：
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥625.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥373.0 |
| 规格： | 5 mg | 产品价格： | ￥850.0 |
| 规格： | 10 mg | 产品价格： | ￥1360.0 |
| 规格： | 25 mg | 产品价格： | ￥2500.0 |
| 规格： | 50 mg | 产品价格： | ￥4000.0 |
| 规格： | 100 mg | 产品价格： | ￥5600.0 |
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AZD2098
CAS No. : 566203-88-1
MCE 国际站：AZD2098
产品活性：AZD2098 是一种有效、选择性的 CCR4 抑制剂，作用于人类、大鼠、小鼠、狗的 CCR4 pIC50s 值分别为 7.8、8.0、8.0、7.6，可用于哮喘研究。
研究领域：GPCR/G Protein | Immunology/Inflammation
作用靶点：CCR
In Vitro: AZD2098 potently inhibits chemokine-induced cellular responses, with pIC50 of 7.5 and 6.3 against CCL22-induced Ca2+ influx in hCCR4-expressing CHO cells and CCL17- or CCL22-induced chemotaxis of primary human Th2 cells respectively.
In Vivo: AZD2098 (73.5-5.0 μg/kg; p.o.; BID; twice a day; 1 hour before and every 12 hours after antigen challenge) exhibits efficacy against antigen-induced inflammatory response among ovalbumin-sensitized rats, and the changes are first visible at a dose of 0.22 µmol/kg and maximal at 7.5 µmol/kg.
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文献和实验Characterization of the Picrotoxin Site of GABAA Receptors
. 2012. AZD‐3043: A novel, metabolically labile sedative‐hypnotic agent with rapid and predictable emergence from hypnosis. Anesthesiology 116:1267‐1277. Elliott, K.A.C
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