Terlipressin
CAS No. | 14636-12-5 | Cat. No. | BCP02061 |
Name | Terlipressin | ||
Synonyms | Glypressin;Gly Gly Gly 8 Lys vasopressin; | ||
Formula | C52H74N16O15S2 | M. Wt | 1227.37 |
Description | Terlipressin is a synthetic triglycyllysine derivative of vasopressin with vasoconstrictive, antihemorrhagic, and antidiuretic properties. Upon intravenous administration, terlipressin, an inactive prodrug, is biotransformed to its active moiety, lysine vasopressin (LVP), a nonselective vasopressin analogue with affinity for vasopressin receptors V1 (V1a), V2 and V3 (V1b). As a V1 agonist, terlipressin increases systemic vascular resistance, particularly in the splanchnic area, resulting in a decrease of portal pressure. V1 binding also promotes platelet aggregation and glycogenolysis, while V3 binding induces adrenocorticotropic hormone (ACTH) secretion. Compared to vasopressin, terlipressin has a minimal effect on V2 receptors, which are responsible for promotion of water reabsorption in the collecting ducts of the kidney via stimulation of cyclic AMP production. | ||
Pathways | GPCR/G Protein | ||
Targets | Vasopressin Receptor |
Structure
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