Terlipressin
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[1][2][3][4][5].
Product Specifications
CAS Number
[14636-12-5]
UNSPSC
12352005
Hazard Statement
H302-H312-H332
Target
Vasopressin Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein
Applications
COVID-19-immunoregulation
Field of Research
Endocrinology; Inflammation/Immunology; Cardiovascular Disease
Assay Protocol
https://www.medchemexpress.com/Terlipressin.html
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
Molecular Formula
C52H74N16O15S2
Molecular Weight
1227.37
Precautions
P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
References & Citations
Shipping Conditions
Blue Ice
Storage Conditions
-80°C, 2 years; -20°C, 1 year (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
V1b Receptor
Available Sizes
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