Ligand id: 2168

Name: vasopressin

Abbreviated name: AVP

Species: Human, Mouse, Rat

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Structure and Physico-chemical Properties

2D Structure
1. Akerlund M, Bossmar T, Brouard R, Kostrzewska A, Laudanski T, Lemancewicz A, Serradeil-Le Gal C, Steinwall M. (1999)
Receptor binding of oxytocin and vasopressin antagonists and inhibitory effects on isolated myometrium from preterm and term pregnant women.
Br J Obstet Gynaecol, 106: 1047-1053. [PMID:10519430]
2. Breton C, Chellil H, Kabbaj-Benmansour M, Carnazzi E, Seyer R, Phalipou S, Morin D, Durroux T, Zingg HH, Barberis C, Mouillac B. (2001)
Direct identification of human oxytocin receptor-binding domains using a photoactivatable cyclic peptide antagonist: comparison with the human V1a vasopressin receptor.
J Biol Chem, 276: 26931-26941. [PMID:11337500]
3. Cheng LL, Stoev S, Manning M, Derick S, Pena A, Mimoun MB, Guillon G. (2004)
Design of potent and selective agonists for the human vasopressin V1b receptor based on modifications of [deamino-cys1]arginine vasopressin at position 4.
J Med Chem, 47: 2375-2388. [PMID:15084136]
4. Chini B, Mouillac B, Ala Y, Balestre MN, Trumpp-Kallmeyer S, Hoflack J, Elands J, Hibert M, Manning M, Jard S et al.. (1995)
Tyr115 is the key residue for determining agonist selectivity in the V1a vasopressin receptor.
EMBO J., 14 (10): 2176-82. [PMID:7774575]
5. Chini B, Mouillac B, Balestre M-N, Trumpp-Kallmeyer S, Hoflack J, Hibert M, Andriolo M, Pupier S, Jard S, Barberis C. (1996)
Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin.
FEBS letters., 397: 201-206. [PMID:8955347]
6. Cotte N, Balestre MN, Aumelas A, Mahe E, Phalipou S, Morin D, Hibert M, Manning M, Durroux T, Barberis C, Mouillac B. (2000)
Conserved aromatic residues in the transmembrane region VI of the V1a vasopressin receptor differentiate agonist vs. antagonist ligand binding.
Eur J Biochem, 267: 4253-4263. [PMID:10866830]
7. Derick S, Cheng LL, Stoev S, Voirol MJ, Ben Mimoun M, Andres M, Gaillard R, Guillon G, Manning M. (2002)
[1-Deamino-4-Cyclohexylalanine]Arginine vasopressin: a potent and specific agonist for vasopressin V1b receptors.
Endocrinology., 143: 4655-4664. [PMID:12446593]
8. Griffante C, Green A, Curcuruto O, Haslam CP, Dickinson BA, Arban R. (2005)
Selectivity of d[Cha4]AVP and SSR149415 at human vasopressin and oxytocin receptors: evidence that SSR149415 is a mixed vasopressin V1b/oxytocin receptor antagonist.
Br J Pharmacol, 146: 744-751. [PMID:16158071]
9. Jasper JR, Harrell CM, O'Brien JA, Pettibone DJ. (1995)
Characterization of the human oxytocin receptor stably expressed in 293 human embryonic kidney cells.
Life Sci, 57: 2253-2261. [PMID:7475979]
10. Nakamura S, Yamamura Y, Itoh S, Hirano T, Tsujimae K, Aoyama M, Kondo K, Ogawa H, Shinohara T, Kan K, Tanada Y, Teramoto S, Sumida T, Nakayama S, Sekiguchi K, Kambe T, Tsujimoto G, Mori T, Tominaga M. (2000)
Characterization of a novel nonpeptide vasopressin V(2)-agonist, OPC-51803, in cells transfected human vasopressin receptor subtypes.
Br J Pharmacol, 129: 1700-1706. [PMID:10780976]
11. Phalipou S, Cotte N, Carnazzi E, Seyer R, Mahe E, Jard S, Barberis C. (1997)
Mapping peptide binding domains of the human V1a vasopressin receptor with a photoactivatable linear peptide antagonist.
J Biol Chem, 272: 26536-26544. [PMID:9334232]
12. Saito M, Tahara A, Sugimoto T. (1997)
1-desamino-8-D-arginine vasopressin (DDAVP) as an agonist on V1b vasopressin receptor.
Biochem Pharmacol, 53: 1711-1717. [PMID:9264324]
13. Serradeil-Le Gal C, Raufaste D, Double-Cazanave E, Guillon G, Garcia C, Pascal M, Maffrand JP. (2000)
Binding properties of a selective tritiated vasopressin V2 receptor antagonist, [H]-SR 121463.
Kidney Int, 58: 1613-1622. [PMID:11012895]
14. Tahara A, Saito M, Sugimoto J, Tomura Y, Wada KI, Kusayama T, Tsukada J, Ishii I, Yatsu T, Uchida W, Tanaka A. (1998)
Pharmacological characterization of the human vasopressin receptor subtypes stably expressed in chinese hamster ovary cells.
Br J Pharmacol, 125: 1463-1470. [PMID:9884074]
15. Tahara A, Saito M, Sugimoto T, Tomura Y, Wada K, Kusayama T, Tsukada J, Ishii N, Yatsu T, Uchida W, Tanaka A. (1998)
Pharmacological characterization of YM087, a potent, nonpeptide human vasopressin V1A and V2 receptor antagonist.
Naunyn Schmiedebergs Arch Pharmacol, 357: 63-69. [PMID:9459574]
16. Thibonnier M, Auzan C, Madhun Z, Wilkins P, Berti-Mattera L, Clauser E. (1994)
Molecular cloning, sequencing, and functional expression of a cDNA encoding thehuman V1a vasopressin receptor.
J Biol Chem, 269: 3304-3310. [PMID:8106369]
17. Thibonnier M, Preston JA, Dulin N, Wilkins PL, Berti-Matera LN, Mattera R. (1997)
The human V3 pituitary vasopressin receptor: ligand binding profile and density-dependent signaling pathways.
Endocrinology., 138: 4109-4122. [PMID:9322919]
18. Yamamura Y, Nakamura S, Itoh S, Hirano T, Onogawa T, Yamashita T, Yamada Y, Tsujimae K, Aoyama M, Kotosai K, Ogawa H, Yamashita H, Kondo K, Tominaga M, Tsujimoto G, Mori T. (1998)
OPC-41061, a highly potent human vasopressin V2-receptor antagonist: pharmacological profile and aquaretic effect by single and multiple oral dosing in rats.
J Pharmacol Exp Ther, 287: 860-867. [PMID:9864265]