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CAY10640 (sEH inhibitor-1)一种有效的、具有口服活性、可溶于水的环氧化物水解酶 (sEH) 抑制剂,对人和鼠中的sEH 具有抑制作用,IC50s 分别为 0.4 和 5.3 nM。

CAY10640 (sEH inhibitor-1)一种有效的、具有口服活性、可溶于水的环氧化物水解酶 (sEH) 抑制剂,对人和鼠中的sEH 具有抑制作用,IC50s 分别为 0.4 和 5.3 nM。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 1 mg | ¥ 861  | In stock | |
| 5 mg | ¥ 2,180  | In stock | |
| 10 mg | ¥ 3,200  | In stock | |
| 25 mg | ¥ 5,090  | In stock | |
| 50 mg | ¥ 6,860  | In stock | |
| 100 mg | ¥ 9,230  | In stock | |
| 200 mg | ¥ 12,300  | In stock | 
CAY10640 相关产品
| 产品描述 | CAY10640 (sEH inhibitor-1) is a potent, orally active, water-soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in humans and mice with IC50s of 0.4 and 5.3 nM, respectively.  | 
| 靶点活性 |  sEH (mouse):0.4 nM  | 
| 体内活性 | 经口给予小鼠13 1-aryl-3-(1-acylpiperidin-4-yl)urea (CAY10640)抑制剂,相较于之前报道的1-adamantylurea基抑制剂,在药代动力学参数上显著改善。这种新型sEH抑制剂在通过体内卡拉胶诱导的炎症疼痛模型测量机械撤退阈值时,其药效比吗啡提高了1000倍,可减轻痛觉过敏。[1]  | 
| 别名 | sEH inhibitor-1 | 
| 分子量 | 371.35 | 
| 分子式 | C17H20F3N3O3 | 
| CAS No. | 1208549-68-1 | 
| Smiles | C(=O)(C1CC1)N2CCC(NC(NC3=CC=C(OC(F)(F)F)C=C3)=O)CC2 | 
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMF: 4.5 mg/mL (12.12 mM), Sonication is recommended.  Ethanol: 2 mg/mL (5.39 mM), Sonication is recommended.  DMSO: 4.5 mg/mL (12.12 mM), Sonication is recommended.   | |||||||||||||||||||||||||
溶液配制表  | ||||||||||||||||||||||||||
Ethanol/DMF/DMSO 
 DMF/DMSO 
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