Ramipril
An ACE inhibitor used to treat high blood pressure, heart failure, and to reduce the risk of cardiovascular events in people with coronary artery disease. It works by relaxing blood vessels and reducing the workload on the heart.
आणविक भार
416.5120 g/mol
LogP
1.40
TPSA
95.90 Ų
लिपिंस्की RO5
उत्तीर्ण
चिकित्सीय क्षेत्र
दवा वर्ग
क्रिया का तंत्र
Prodrug converted to ramiprilat; ACE inhibitor.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Prodrug converted to ramiprilat; ACE inhibitor.
2D संरचना
Cite this structure
Embed this structure
SMILES
CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N1[C@H](C(=O)O)C[C@@H]2CCC[C@@H]21
InChI
InChI=1S/C23H32N2O5/c1-3-30-23(29)18(13-12-16-8-5-4-6-9-16)24-15(2)21(26)25-19-11-7-10-17(19)14-20(25)22(27)28/h4-6,8-9,15,17-20,24H,3,7,10-14H2,1-2H3,(H,27,28)/t15-,17-,18-,19-,20-/m0/s1
Molecular Formula
C23H32N2O5
HBD / HBA
2 / 6
घूर्णनीय बंधन
10
भारी परमाणु
30
Ramipril, an ACE inhibitor, reduces lithium renal clearance through decreased glomerular filtration, leading to potentially toxic lithium accumulation.
Combining empagliflozin with an ACE inhibitor such as ramipril can cause additive blood pressure reduction and volume depletion, increasing the risk of hypotension and acute kidney injury.
No side effects recorded
Side effect data is not yet available for this drug.
अक्सर पूछे जाने वाले प्रश्न
An ACE inhibitor used to treat high blood pressure, heart failure, and to reduce the risk of cardiovascular events in people with coronary artery disease. It works by relaxing blood vessels and reducing the workload on the heart.
Prodrug converted to ramiprilat; ACE inhibitor.
Key pharmacokinetic parameters for Ramipril: Half-life: 13-17 hours.
Yes, Ramipril is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
Related Drugs
Same Drug Class
Same Target
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1168. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5362129. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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