Ethacrynic Acid

CHEMBL456 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
303.1 g/mol
LogP
3.8
Phase
4

This loop diuretic works by blocking salt reabsorption in the kidneys, causing the body to excrete more sodium and water in the urine. It is used to treat fluid overload in conditions such as heart failure and kidney disease.

分子量

303.1300 g/mol

LogP

3.80

TPSA

63.60 Ų

リピンスキーの五則

適合

治療領域

作用機序

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

2D構造

SVG PNG

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SMILES

C=C(CC)C(=O)c1ccc(OCC(=O)O)c(Cl)c1Cl

InChI

InChI=1S/C13H12Cl2O4/c1-3-7(2)13(18)8-4-5-9(12(15)11(8)14)19-6-10(16)17/h4-5H,2-3,6H2,1H3,(H,16,17)

Molecular Formula

C13H12Cl2O4

HBD / HBA

1 / 4

回転可能結合数

6

重原子数

19

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.

よくある質問

This loop diuretic works by blocking salt reabsorption in the kidneys, causing the body to excrete more sodium and water in the urine. It is used to treat fluid overload in conditions such as heart failure and kidney disease.

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

Yes, Ethacrynic Acid 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). CHEMBL456. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3278. Chemical information database.

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

医学的免責事項

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.