Tolvaptan

CHEMBL344159 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
448.9 g/mol
LogP
4.8
Phase
4

Tolvaptan is a selective vasopressin V2 receptor antagonist (vaptans class) that blocks the antidiuretic action of arginine vasopressin (AVP) in the renal collecting duct, preventing water reabsorption and promoting free water excretion (aquaresis) without significant sodium or potassium loss. It is approved for hyponatremia in syndrome of inappropriate ADH secretion (SIADH), congestive heart failure, and cirrhosis, and for slowing kidney cyst growth in autosomal dominant polycystic kidney disease (ADPKD). Its aquaretic mechanism corrects hyponatremia and reduces cyst expansion without the electrolyte disturbances of conventional diuretics.

Berat Molekul

448,9000 g/mol

LogP

4,80

TPSA

69,60 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Struktur 2D

SVG PNG

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SMILES

Cc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCC(O)c3cc(Cl)ccc32)c(C)c1

InChI

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)

Molecular Formula

C26H25ClN2O3

HBD / HBA

2 / 3

Ikatan yang Dapat Dirotasi

3

Atom Berat

32

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Pertanyaan yang Sering Diajukan

Tolvaptan is a selective vasopressin V2 receptor antagonist (vaptans class) that blocks the antidiuretic action of arginine vasopressin (AVP) in the renal collecting duct, preventing water reabsorption and promoting free water excretion (aquaresis) without significant sodium or potassium loss. It is approved for hyponatremia in syndrome of inappropriate ADH secretion (SIADH), congestive heart failure, and cirrhosis, and for slowing kidney cyst growth in autosomal dominant polycystic kidney disease (ADPKD). Its aquaretic mechanism corrects hyponatremia and reduces cyst expansion without the …

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Tolvaptan is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL344159. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 216237. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Penyangkalan Medis

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.