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Captopril

Angiotensin Converting Enzyme Inhibitor — CARDIOVASCULAR SYSTEM

Also known as: (-)-Captopril, L-Captopril, lopirin, S-Captopril, SQ 14225, SQ-14225, SQ14225

OfpFDA approvedATC C09AA01ATC C09BA01

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 classAngiotensin Converting Enzyme Inhibitor

Molecular targets (13)

TargetGeneActionActivity
Angiotensin-converting enzymeACEunknownKi 8.77
ReninRENunknownKi 8.77
Angiotensin-converting enzymeACEinhibitorKi 8.70
Angiotensin-converting enzymeAceunknownKi 8.70
ProthrombinF2unknownKi 7.32
Leukotriene A-4 hydrolaseLTA4HunknownIC50 7.15
Beta-lactamase class B VIM-2blaVIM-2unknownKd 6.22
Succinyl-diaminopimelate desuccinylasedapEunknownKi 5.74
Beta-lactamaseblaIMP-1unknownKi 5.62
Prostaglandin G/H synthase 2PTGS2unknownKi 4.92
Beta-lactamase NDM-1blaNDM-1unknownKd 4.85
Prostaglandin G/H synthase 1PTGS1unknownKi 4.77
Beta-lactamase IIbla2unknownKi 4.75

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
1981-04-06FDA—PAR PHARM

ATC classification

ATC codeTherapeutic hierarchy
C09AA01CARDIOVASCULAR SYSTEM › AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM › ACE INHIBITORS, PLAIN › ACE inhibitors, plain
C09BA01CARDIOVASCULAR 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 termLLR
Cardiac failure congestive132.9
Segmental diverticular colitis98.1
Pedal pulse abnormal90.8
Myocardial infarction85.1
Hypokalaemia77.7
Cyanosis77.6
Hyponatraemia75.0
Renal failure74.8
Calcium ionised decreased73.3
Reduced facial expression72.2
Toxic epidermal necrolysis71.6
Scleroderma renal crisis66.3

Chemical structure

Molecular formulaC9H15NO3S
Molecular weight217.29 g/mol
CAS number—
InChIKeyFAKRSMQSSFJEIM-RQJHMYQMSA-N
PubChem CID44093
C[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O

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

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

StatusOFP
First approval1981-04-06
AgencyFDA
Targets13
Indications4
FormulaC9H15NO3S
DrugCentral ID484
Interactive profile