| 货号 | 包装规格 | 操作 |
|---|---|---|
| C2917-.1MG | 0.1 mg |
≥97%（HPLC法）
与大鼠CRF 2 α受体的亲和力比人CRF 2 α受体高10倍。
The corticotropin releasing factor (CRF) antagonist α-helical CRF [9-41] exhibits 10-fold higher affinity for rat CRF2α receptors over human CRF2α receptors. It has been used to elucidate the role of CRF in various physiological systems. In colonic epithelium, it abolishes CRF-induced changes in ion secretion, and significantly inhibits CRF-stimulated conductance. It antagonizes the CRF-induced proinflammatory degranulation of perivascular mast cells that are activated in response to acute psychological stress and CRF secretion.
从0.1% TFA的H2O溶液中冻干
| 英文名称 | Corticotropin Releasing Factor Antagonist |
| CAS 号 | 99658-03-4 |
| 经验分子式 | C166H274N46O53S2 |
| 分子量 | 3826.36 |
| UNSPSC | 51111800 |
| NACRES | NA.32 |
| MDL 号 | MFCD00081543 |
| 含量测定 | ≥97%（HPLC法） |
| 形态 | 粉末 |
| 储存温度 | −20°C |
| 质量等级 | 200 |
| 基因信息 | 人... CRH（1392）小鼠... CRH（12918）大鼠... CRH（81648） |
| 包装规格（货号 C2917-.1MG） | 0.1 mg |
