ASP-4058
规格
Cas Number | 952565-91-2 |
规格或纯度 | Moligand™, ≥99% |
级别 | Moligand™ |
纯度 | ≥99% |
包装 | 10mg 或 5mg 或 25mg |
产品信息
品牌 | 阿拉丁 |
溶解性 | DMSO : ≥ 50 mg/mL (113.04 mM) |
过滤标签 | LPL Receptor,GPCR/G Protein |
储存温度 | 避光,-80℃储存 |
运输条件 | 超低温冰袋运输 |
生化和生理学机理 | ASP-4058 是一种新一代的选择性口服生物活性激动剂,可激动磷酸脑啡肽受体 1 和 5(S1P 1 和 S1P 5),改善啮齿类动物实验性自身免疫性脑脊髓炎,并具有良好的安全性。 |
英文描述 |
ASP-4058 is a next-generation, selective and oral bioactive agonist for Sphingosine 1-Phosphate receptors 1 and 5 (S1P 1 and S1P 5 ) , ameliorates rodent experimental autoimmune encephalomyelitis with a favorable safety profile In Vivo ASP4058 (p.o., daily for 21 days) reduces the clinical score in a dose-dependent manner and the cumulative clinical score from day 0 to 21 dpi at 0.03, 0.1 and 0.3 mg/kg are 15.5±1.48, 9.50±2.17 and 1.17±1.17, respectively, while that of vehicle-treated group is 15.5±0.619 in rats. ASP4058 prevents decreases in body weight of EAE rats . ASP4058 (p.o., daily for day 12 to day 45) maintains the clinical score at a relatively low level and the cumulative clinical scores (18-45 dpi) among the groups treated with 0.1 and 0.3 mg/kg dosages are 6.90±2.85 and 5.60±2.21, respectively in mice. The ED50 values for ASP4058 is 0.063 mg/kg . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male Lewis rats with an induction of EAE . Dosage: 0.03, 0.1 or 0.3 mg/kg. Administration: Oral administration once daily for 21 days. Result: Reduced the clinical score in a dose-dependent manner and the cumulative clinical score. Animal Model: SJL mice immunized with PLP139-151 and boosted with pertussis toxin developed relapsing-remitting EAE . Dosage: 0.1 and 0.3 mg/kg Administration: Oral administration once daily from day 12 to day 45. Result: Maintained the clinical score at a relatively low level and the cumulative clinical scores (18-45 dpi). Form:Solid IC50& Target:S1P 1 and S1P 5 |