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Chlortalidone

Thiazide-like Diuretic — CARDIOVASCULAR SYSTEM

Also known as: chlorphthalidolone, chlorthalidon, chlorthalidone, clortalidone, phthalamudine

OfpFDA approvedATC C03BA04ATC C03BB04ATC C03EA06

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Chlortalidone is an ofp drug in the Thiazide-like Diuretic class catalogued in DrugCentral. It was first approved by the FDA in 1960. DrugCentral lists 14 molecular targets, including CA7, CA12 and CA5B. Recorded indications include Edema, Hypertensive disorder, Peripheral Edema due to Chronic Heart Failure and Pulmonary Edema due to Chronic Heart Failure.

  • Approval status: ofp (first approved 1960 by the FDA).
  • Drug class: Thiazide-like Diuretic.
  • Molecular targets: CA7, CA12, CA5B and Ca13 (14 listed in DrugCentral).
  • Indications: Edema, Hypertensive disorder, Peripheral Edema due to Chronic Heart Failure and Pulmonary Edema due to Chronic Heart Failure.
  • ATC code: C03BA04 (Sulfonamides, plain).
  • Molecular formula: C14H11ClN2O4S; molecular weight 338.76 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (4)

  • Edema
  • Hypertensive disorder
  • Peripheral Edema due to Chronic Heart Failure
  • Pulmonary Edema due to Chronic Heart Failure

Off-label uses (2)

  • Calcium renal calculus
  • Diabetes insipidus

Contraindications (47)

  • Acute nephropathy
  • Acute pancreatitis
  • Acutely Decompensated HF Requiring Parenteral Inotropic Therapy
  • Anaphylaxis
  • Anuria
  • Asthma
  • Atrioventricular block
  • Calculus in biliary tract
  • Cardiogenic shock
  • Cerebrovascular disease
  • Chronic disease of respiratory system
  • Chronic heart failure
  • Chronic myocardial ischemia
  • Complete atrioventricular block
  • Conduction disorder of the heart
  • Depressive disorder
  • Diabetes mellitus type 1
  • Diabetes mellitus type 2
  • Electroconvulsive therapy
  • End stage renal disease
  • Epilepsy
  • First Degree Atrioventricular Heart Block
  • Gout
  • Hepatic failure
  • Hypercalcemia
  • Hypercholesterolemia
  • Hyperuricemia
  • Hypochloremic alkalosis
  • Hypokalemia
  • Hypomagnesemia
  • + 17 more

Mechanism & targets

Established pharmacologic classThiazide-like Diuretic

Molecular targets (14)

TargetGeneActionActivity
Carbonic anhydrase 7CA7unknownKi 8.55
Carbonic anhydrase 12CA12unknownKi 8.35
Carbonic anhydrase 5B, mitochondrialCA5BunknownKi 8.05
Carbonic anhydrase 13Ca13unknownKi 7.82
Carbonic anhydrase 9CA9unknownKi 7.64
Carbonic anhydrase 4CA4unknownKi 6.71
Carbonic anhydrase 1CA1unknownKi 6.46
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase DNAPEPLDallosteric modulatorKd 6.17
Carbonic anhydrase 5A, mitochondrialCA5AunknownKi 6.04
Carbonic anhydrase 6CA6unknownKi 5.87
Carbonic anhydrase 2CA2unknownKd 5.56
Carbonic anhydrase 14CA14unknownKi 5.38
Carbonic anhydrase 3CA3unknownKi 4.96
Solute carrier family 12 member 3SLC12A3inhibitor—

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
1960-04-07FDA——

ATC classification

ATC codeTherapeutic hierarchy
C03BA04CARDIOVASCULAR SYSTEM › DIURETICS › LOW-CEILING DIURETICS, EXCL. THIAZIDES › Sulfonamides, plain
C03BB04CARDIOVASCULAR SYSTEM › DIURETICS › LOW-CEILING DIURETICS, EXCL. THIAZIDES › Sulfonamides and potassium in combination
C03EA06CARDIOVASCULAR SYSTEM › DIURETICS › DIURETICS AND POTASSIUM-SPARING AGENTS IN COMBINATION › Low-ceiling diuretics and potassium-sparing agents

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
Hyponatraemia442.1
Hypokalaemia261.2
Renal artery stenosis103.8
Presyncope96.1
Lichen planopilaris95.7
Renal cyst haemorrhage94.5
Renal impairment88.8
Meningitis aseptic84.7
Acute kidney injury81.1
SARS-CoV-2 antibody test positive79.7
Abdominal wall haemorrhage75.7
Vena cava injury75.4

Chemical structure

Full physicochemical, ADMET and 3D-structure analysis of Chlortalidone is on its molecule page.

Molecular formulaC14H11ClN2O4S
Molecular weight338.76 g/mol
CAS number77-36-1
InChIKeyJIVPVXMEBJLZRO-UHFFFAOYSA-N
PubChem CID2732
NS(=O)(=O)C1=CC(=CC=C1Cl)C1(O)NC(=O)C2=CC=CC=C12

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Chlortalidone used for?

DrugCentral lists the following indications for Chlortalidone: Edema, Hypertensive disorder, Peripheral Edema due to Chronic Heart Failure and Pulmonary Edema due to Chronic Heart Failure.

How does Chlortalidone work?

Its molecular targets in DrugCentral include CA7, CA12, CA5B and Ca13.

When was Chlortalidone first approved?

Chlortalidone was first approved by the FDA in 1960.

What drug class does Chlortalidone belong to?

Chlortalidone is in the Thiazide-like Diuretic class.

What is the chemical formula of Chlortalidone?

Chlortalidone has the molecular formula C14H11ClN2O4S and a molecular weight of 338.76 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 approval1960-04-07
AgencyFDA
Targets14
Indications4
FormulaC14H11ClN2O4S
DrugCentral ID625
Interactive profile