Conivaptan Hydrochloride

CHEMBL1201108 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
535.0 g/mol
LogP
Phase
4

The hydrochloride salt form of conivaptan used intravenously in hospital settings to correct euvolemic or hypervolemic hyponatremia. It blocks vasopressin receptors in the kidneys to increase water excretion and raise blood sodium levels.

Moleküler Ağırlık

535,0000 g/mol

TPSA

78,10 Ų

Terapötik Alanlar

Etki Mekanizması

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

2D Yapı

SVG PNG

Cite this structure


                        

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SMILES

Cc1nc2c([nH]1)-c1ccccc1N(C(=O)c1ccc(NC(=O)c3ccccc3-c3ccccc3)cc1)CC2.Cl

InChI

InChI=1S/C32H26N4O2.ClH/c1-21-33-28-19-20-36(29-14-8-7-13-27(29)30(28)34-21)32(38)23-15-17-24(18-16-23)35-31(37)26-12-6-5-11-25(26)22-9-3-2-4-10-22;/h2-18H,19-20H2,1H3,(H,33,34)(H,35,37);1H

Molecular Formula

C32H27ClN4O2

HBD / HBA

3 / 3

Döndürülebilir Bağlar

4

Ağır Atomlar

39

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.

Sıkça Sorulan Sorular

The hydrochloride salt form of conivaptan used intravenously in hospital settings to correct euvolemic or hypervolemic hyponatremia. It blocks vasopressin receptors in the kidneys to increase water excretion and raise blood sodium levels.

Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.

Yes, Conivaptan Hydrochloride 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). CHEMBL1201108. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 216322. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tıbbi Sorumluluk Reddi

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.