Fosinopril Sodium

CHEMBL3039596 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
585.6 g/mol
LogP
Phase
4

This sodium salt form of fosinopril is an ACE inhibitor used to lower high blood pressure and treat heart failure by reducing the production of angiotensin II, which narrows blood vessels. Unlike many other ACE inhibitors, it is eliminated through both the liver and kidneys, making dosing adjustments less critical in kidney impairment.

Masse moléculaire

585,6000 g/mol

TPSA

113,00 Ų

Aires thérapeutiques

Mécanisme d'action

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

Structure 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CCC(=O)O[C@@H](O[P@](=O)(CCCCc1ccccc1)CC(=O)N1C[C@H](C2CCCCC2)C[C@H]1C(=O)[O-])C(C)C.[Na+]

InChI

InChI=1S/C30H46NO7P.Na/c1-4-28(33)37-30(22(2)3)38-39(36,18-12-11-15-23-13-7-5-8-14-23)21-27(32)31-20-25(19-26(31)29(34)35)24-16-9-6-10-17-24;/h5,7-8,13-14,22,24-26,30H,4,6,9-12,15-21H2,1-3H3,(H,34,35);/q;+1/p-1/t25-,26+,30+,39-;/m1./s1

Molecular Formula

C30H45NNaO7P

HBD / HBA

- / 7

Liaisons Rotatives

15

Atomes Lourds

40

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.

Foire aux questions

This sodium salt form of fosinopril is an ACE inhibitor used to lower high blood pressure and treat heart failure by reducing the production of angiotensin II, which narrows blood vessels. Unlike many other ACE inhibitors, it is eliminated through both the liver and kidneys, making dosing adjustments less critical in kidney impairment.

Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.

Yes, Fosinopril Sodium 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). CHEMBL3039596. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 23681451. Chemical information database.

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

Avertissement médical

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.