Fig. 1 · Structure
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Terlipressin acetate
Vasopressin V1 Receptor Agonist
Terlipressin acetate is a selective agonist of the vasopressin V1 receptor, known for its strong vasoconstrictive effects. This compound effectively reduces splanchnic blood flow and portal pressure, making it useful in the management of acute variceal bleeding. Additionally, terlipressin exhibits anti-inflammatory and antioxidative properties, highlighting its potential in research related to hepatorenal syndrome and norepinephrine-resistant septic shock.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Agonist |
| CAS Number | 914453-96-6 |
| Applications | Vasopressin V1 Receptor Agonist |
| Formula | C52H72N16O16S2.(C2H6O)x |
| Molecular Weight | 1227.37 (free base) |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
Preparing Stock Solutions
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.