Terlipressin

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Chemical Information

Product name：Terlipressin	Purity：98% min
CAS NO：14636-12-5	Solubility：DMSO : 100 mg/mL (81.48 mM)
Molecular Formula：C₅₂H₇₄N₁₆O₁₅S₂	Package：Package according to customer requirements
Molecular Weight：1227.37	Storage：Store at -20℃

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Remarks

Terlipressin is a vasopressin analogue with potent vasoactive properties. Terlipressin is a highly selective vasopressin V1 receptor agonist that reduces the splanchnic blood flow and portal pressure and controls acute variceal bleeding. Terlipressin exerts anti-inflammatory and anti-oxidative effects. Terlipressin has the potential for hepatorenal syndrome and norepinephrine-resistant septic shock research.

Related Products:

Plecanatide; Linaclotide; Carbetocin; Octreotide acetate; Cetrorelix; Desmopressin; Desmopressin acetate; Degarelix; Goserelin acetate; Ganirelix Acetate; Abarelix; GLP-1 (7-37); Semaglutide

References

[1]. Zi-Meng Liu, et al. Terlipressin Protects Intestinal Epithelial Cells Against Oxygen-Glucose Deprivation/Re-Oxygenation Injury via the Phosphatidylinositol 3-kinase Pathway. Exp Ther Med. 2017 Jul;14(1):260-266.

[2]. Yeun Tarl Fresner Ng Jao, et al. Refractory Torsade De Pointes Induced by Terlipressin (Glypressin). Int J Cardiol. 2016 Nov 1;222:135-140.

[3]. Xiqiang Liu, et al. Signaling Through Hepatocyte Vasopressin Receptor 1 Protects Mouse Liver From Ischemia-Reperfusion Injury. Oncotarget. 2016 Oct 25;7(43):69276-69290.