货号 | 3126/1 |
供应商 | Tocris |
生物活性 | Potent and selective human vasopressin V1B receptor agonist (Ki values are 1.2, 151, 240 and 750 nM for V1B, V1A, Oxytocin and V2 receptors respectively). Stimulates ACTH and corticosterone secretion and exhibits negligible vasopressor activity in vivo. |
运输条件 | Blue Ice |
存放说明 | -20℃ |
计算分子量 | 1094.31 |
分子式 | C50H71N13O11S2 |
可溶性/溶解性 | Soluble to 1 mg/ml in water |
CAS号 | 500170-27-4 |
序列号 | XYFXNCPRG (Modifications: X-1 = Mpr, X-4 = Cha, Gly-9 = C-terminal amide, Disulfide bridge between X-1 - Cys-6) |
参考文献 | Penaet al (2007) Design and synthesis of the frist selective agonists for the rat vasopressin V1b receptor: based on modifications of deamino-[cys1]arginine vasopressin at positions 4 and 8. J.Med.Chem. 50 835. PMID: 17300166. Chenget al (2004) Design of potent and selective agonists for the human vasopressin V1b receptor based on modifications of [deamino-cys1]arginine vasopressin at position 4. J.Med.Chem. 47 2375. PMID: 15084136. Dericket al (2002) [1-Deamino-4-cyclohexylalanine] arginine vasopressin: a potent and specific agonist for vasopressin V1b receptors. Endocrinology 143 4655. PMID: 12446593. |