(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin
CAS No. 73168-24-8
(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin ( —— )
产品货号. M30829 CAS No. 73168-24-8
Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo.
-
产品描述Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo.
-
体外实验——
-
体内实验——
-
同义词——
-
通路GPCR/G Protein
-
靶点Vasopressin Receptor
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number73168-24-8
-
分子量1151.38
-
分子式C52H74N14O12S2
-
纯度>98% (HPLC)
-
溶解度water:2 mg/mL
-
SMILESCOC1=CC=C(C[C@@H]2NC(=O)CC3(CCCCC3)SSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC3=CC=CC=C3)NC2=O)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(N)=O)C=C1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Kruszynski et al (1980) [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine]arginine-vasopressin and [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid)]arginine-vasopressin, two highly potent antagonists of the vas J.Med.Chem. 23 364 PMID: 6892930
产品手册
关联产品
-
Desmopressin
去氨加压素 (DDAVP) 是抗利尿激素精氨酸加压素的合成类似物。加压素受体 去氨加压素的抗利尿特性导致其用于治疗多尿性疾病,包括原发性夜间遗尿症、夜尿症和尿崩症。
-
d[Cha4]-AVP
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.
-
Terlipressin Acetate
特利加压素是一种高选择性加压素 V1 受体激动剂,可抑制缺氧和葡萄糖剥夺/再氧合 (OGD/R) 引起的肠上皮细胞损伤 (IEC-6)。
021-51111890
购物车()
sales@molnova.cn

