Captopril
Angiotensin Converting Enzyme Inhibitor — CARDIOVASCULAR SYSTEM
Also known as: (-)-Captopril, L-Captopril, lopirin, S-Captopril, SQ 14225, SQ-14225, SQ14225
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Captopril is an ofp drug in the Angiotensin Converting Enzyme Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 1981. Its mechanism of action is classified as Angiotensin-converting Enzyme Inhibitors. DrugCentral lists 13 molecular targets, including ACE, REN and ACE. Recorded indications include Chronic heart failure, Diabetic renal disease, Hypertensive disorder and Left ventricular cardiac dysfunction.
- Approval status: ofp (first approved 1981 by the FDA).
- Drug class: Angiotensin Converting Enzyme Inhibitor.
- Mechanism of action: Angiotensin-converting Enzyme Inhibitors.
- Molecular targets: ACE, REN, ACE and Ace (13 listed in DrugCentral).
- Indications: Chronic heart failure, Diabetic renal disease, Hypertensive disorder and Left ventricular cardiac dysfunction.
- ATC code: C09AA01 (ACE inhibitors, plain).
- Molecular formula: C9H15NO3S; molecular weight 217.29 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (4)
- Chronic heart failure
- Diabetic renal disease
- Hypertensive disorder
- Left ventricular cardiac dysfunction
Off-label uses (5)
- Atrial fibrillation
- Cystine Renal Calculi
- Cystinuria
- Diastolic heart failure
- Nondiabetic Proteinuric Nephropathy
Contraindications (38)
- Acute cerebrovascular insufficiency
- Acute pancreatitis
- Angioedema
- Anuria
- Aortic valve stenosis
- Azotemia
- Bone marrow depression
- Cough
- Dehydration
- Diabetes mellitus
- Disease of liver
- Disorder of connective tissue
- Gout
- Hemodialysis with High-Flux Membrane
- Hepatic coma
- Hereditary angioneurotic edema
- Hypercalcemia
- Hypercholesterolemia
- Hyperkalemia
- Hyperparathyroidism
- Hypertrophic cardiomyopathy
- Hyperuricemia
- Hypochloremic alkalosis
- Hypokalemia
- Hypomagnesemia
- Hyponatremia
- Hypovolemia
- Immunosuppression
- Kidney disease
- Low blood pressure
- + 8 more
Mechanism & targets
| Mechanism of action (MoA) | Angiotensin-converting Enzyme Inhibitors |
|---|---|
| Established pharmacologic class | Angiotensin Converting Enzyme Inhibitor |
Molecular targets (13)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Angiotensin-converting enzyme | ACE | unknown | Ki 8.77 |
| Renin | REN | unknown | Ki 8.77 |
| Angiotensin-converting enzyme | ACE | inhibitor | Ki 8.70 |
| Angiotensin-converting enzyme | Ace | unknown | Ki 8.70 |
| Prothrombin | F2 | unknown | Ki 7.32 |
| Leukotriene A-4 hydrolase | LTA4H | unknown | IC50 7.15 |
| Beta-lactamase class B VIM-2 | blaVIM-2 | unknown | Kd 6.22 |
| Succinyl-diaminopimelate desuccinylase | dapE | unknown | Ki 5.74 |
| Beta-lactamase | blaIMP-1 | unknown | Ki 5.62 |
| Prostaglandin G/H synthase 2 | PTGS2 | unknown | Ki 4.92 |
| Beta-lactamase NDM-1 | blaNDM-1 | unknown | Kd 4.85 |
| Prostaglandin G/H synthase 1 | PTGS1 | unknown | Ki 4.77 |
| Beta-lactamase II | bla2 | unknown | Ki 4.75 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1981-04-06 | FDA | — | PAR PHARM |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C09AA01 | CARDIOVASCULAR SYSTEM › AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM › ACE INHIBITORS, PLAIN › ACE inhibitors, plain |
C09BA01 | CARDIOVASCULAR SYSTEM › AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM › ACE INHIBITORS, COMBINATIONS › ACE inhibitors and diuretics |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Cardiac failure congestive | 132.9 |
| Segmental diverticular colitis | 98.1 |
| Pedal pulse abnormal | 90.8 |
| Myocardial infarction | 85.1 |
| Hypokalaemia | 77.7 |
| Cyanosis | 77.6 |
| Hyponatraemia | 75.0 |
| Renal failure | 74.8 |
| Calcium ionised decreased | 73.3 |
| Reduced facial expression | 72.2 |
| Toxic epidermal necrolysis | 71.6 |
| Scleroderma renal crisis | 66.3 |
Chemical structure
| Molecular formula | C9H15NO3S |
|---|---|
| Molecular weight | 217.29 g/mol |
| CAS number | — |
| InChIKey | FAKRSMQSSFJEIM-RQJHMYQMSA-N |
| PubChem CID | 44093 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Captopril used for?
DrugCentral lists the following indications for Captopril: Chronic heart failure, Diabetic renal disease, Hypertensive disorder and Left ventricular cardiac dysfunction.
How does Captopril work?
Captopril is classified as Angiotensin-converting Enzyme Inhibitors; its molecular targets in DrugCentral include ACE, REN, ACE (inhibitor) and Ace.
When was Captopril first approved?
Captopril was first approved by the FDA in 1981.
What drug class does Captopril belong to?
Captopril is in the Angiotensin Converting Enzyme Inhibitor class.
What is the chemical formula of Captopril?
Captopril has the molecular formula C9H15NO3S and a molecular weight of 217.29 g/mol.
Browse: all drugs starting with C · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 484 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1560 — compound record and bioactivity
- PubChem CID 44093 — chemical identifiers
- DrugBank DB01197 — drug record
- FDA UNII 9G64RSX1XD — substance identity
- DailyMed: FDA labels for Captopril — current prescribing information (label search)
- UniProt P00797 (REN) — target protein
- UniProt P12821 (ACE) — target protein
- UniProt P00734 (F2) — target protein
- UniProt P09960 (LTA4H) — target protein
- UniProt P35354 (PTGS2) — target protein
- UniProt P23219 (PTGS1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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