Spirapril

CHEMBL431 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
466.6 g/mol
LogP
0.9
Phase
4

Spirapril is a prodrug angiotensin-converting enzyme (ACE) inhibitor that is hydrolyzed to its active form spiraprilat, used for the treatment of hypertension and heart failure, with investigational properties in stroke prevention. By inhibiting ACE-mediated conversion of angiotensin I to angiotensin II, it reduces vasoconstriction, aldosterone secretion, and sodium retention, lowering blood pressure and cardiac preload and afterload. It has a long duration of action allowing once-daily dosing.

分子量

466.6000 g/mol

LogP

0.90

TPSA

147.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

2D構造

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SMILES

CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1CC2(C[C@H]1C(=O)O)SCCS2

InChI

InChI=1S/C22H30N2O5S2/c1-3-29-21(28)17(10-9-16-7-5-4-6-8-16)23-15(2)19(25)24-14-22(30-11-12-31-22)13-18(24)20(26)27/h4-8,15,17-18,23H,3,9-14H2,1-2H3,(H,26,27)/t15-,17-,18-/m0/s1

Molecular Formula

C22H30N2O5S2

HBD / HBA

2 / 8

回転可能結合数

10

重原子数

31

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

Spirapril is a prodrug angiotensin-converting enzyme (ACE) inhibitor that is hydrolyzed to its active form spiraprilat, used for the treatment of hypertension and heart failure, with investigational properties in stroke prevention. By inhibiting ACE-mediated conversion of angiotensin I to angiotensin II, it reduces vasoconstriction, aldosterone secretion, and sodium retention, lowering blood pressure and cardiac preload and afterload. It has a long duration of action allowing once-daily dosing.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Spirapril 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). CHEMBL431. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5311447. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

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.