Conivaptan Hydrochloride

CHEMBL1201108 Phase 4 Одобрено 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.

Молекулярная масса

535,0000 g/mol

TPSA

78,10 Ų

Терапевтические области

Механизм действия

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Механизм

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

2D Структура

SVG PNG

Cite this structure


                        

Embed this structure


                        

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

Вращаемые Связи

4

Тяжёлые Атомы

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.

Часто задаваемые вопросы

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.

Медицинский отказ от ответственности

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.