(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin
Tocris Bioscience | Catalog # 3377
Key Product Details
Description
Product Description
(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin is a 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.
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The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solubility | Soluble to 2mg/ml in water |
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Background References
References are publications that support the biological activity of the product. See our Citations tab to view 8 publications citing the usage of this product.
- Engin and Treit Dissociation of the anxiolytic-like effects of Avpr1a and Avpr1b receptor antagonists in the dorsal and ventral hippocampus. Neuropeptides 2008 PMID: 18508119
- Spath Arginine vasopressin and oxyt. increase intracellular calcium and cAMP in human glomerular epithelial cells in culture. Kidney Blood Press.Res. 1996 PMID: 8871886
- Tsuchiya Vasopressin inhibits sarcolemmal ATP-sensitive K+ channels via V1 receptors activation in the guinea pig heart. Circ.J. 2002 PMID: 11922278
- Kruszynski [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. 1980 PMID: 6892930
Product Documents
Certificate of Analysis
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Product Specific Notices
For research use only
Citations for (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin
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