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(ES)
Source
CIMA_ES
USDailyMed:Tolvaptan
UK: Contraindicated
C03XA01(WHO)
AU:S4(Prescription only)UK:POM(Prescription only)US:℞-onlyEU:Rx-only
N-(4-{[(5R)-7-Chloro-5-hydroxy-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]carbonyl}-3-methylphenyl)-2-methylbenzamide
150683-30-0N
216237
2226
DB06212Y
187438Y
21G72T1950
D01213
CHEBI:32246
ChEMBL344159Y
DTXSID3048780
Interactive image
Cc1ccccc1C(=O)Nc2cc(C)c(cc2)C(=O)N3c4ccc(Cl)cc4[C@H](O)CCC3
InChI=1S/C26H25ClN2O3/c1-16-6-3-4-7-20(16)25(31)28-19-10-11-21(17(2)14-19)26(32)29-13-5-8-24(30)22-15-18(27)9-12-23(22)29/h3-4,6-7,9-12,14-15,24,30H,5,8,13H2,1-2H3,(H,28,31)YKey:GYHCTFXIZSNGJT-UHFFFAOYSA-NY
Tolvaptan, sold under the brand nameSamscaamong others, is anaquareticdrug that functions as a selective,competitivevasopressin receptor 2 (V2) antagonistused to treathyponatremia(low bloodsodiumlevels) associated withcongestive heart failure,cirrhosis, and thesyndrome of inappropriate antidiuretic hormone(SIADH). Tolvaptan was approved by the U.S.Food and Drug Administration(FDA) on May 19, 2009, and is sold byOtsuka Pharmaceutical Co.under the trade name Samsca.Tolvaptan, as Jynarque, was granted approval for medical use in the United States in April 2018.
The U.S.Food and Drug Administration(FDA) granted tolvaptan afast trackdesignation for clinical trials investigating its use for the treatment ofpolycystic kidney disease.The FDA granted Jynarque anorphan drugdesignation in April 2012, for the treatment ofautosomal dominant polycystic kidney disease.
Tolvaptan is available as ageneric medication.