Conivaptan Hydrochloride
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.
الوزن الجزيئي
535,0000 g/mol
TPSA
78,10 Ų
المجالات العلاجية
آلية العمل
Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Absorbs, reflects, or scatters ultraviolet radiation before it reaches the skin, protecting against UV-induced DNA damage and sunburn.
البنية ثنائية الأبعاد
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
الروابط القابلة للدوران
4
الذرات الثقيلة
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.
الأسئلة الشائعة
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
- 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.
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