Chlortalidone
Thiazide-like Diuretic — CARDIOVASCULAR SYSTEM
Also known as: chlorphthalidolone, chlorthalidon, chlorthalidone, clortalidone, phthalamudine
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 class | Thiazide-like Diuretic |
|---|
Molecular targets (14)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Carbonic anhydrase 7 | CA7 | unknown | Ki 8.55 |
| Carbonic anhydrase 12 | CA12 | unknown | Ki 8.35 |
| Carbonic anhydrase 5B, mitochondrial | CA5B | unknown | Ki 8.05 |
| Carbonic anhydrase 13 | Ca13 | unknown | Ki 7.82 |
| Carbonic anhydrase 9 | CA9 | unknown | Ki 7.64 |
| Carbonic anhydrase 4 | CA4 | unknown | Ki 6.71 |
| Carbonic anhydrase 1 | CA1 | unknown | Ki 6.46 |
| N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D | NAPEPLD | allosteric modulator | Kd 6.17 |
| Carbonic anhydrase 5A, mitochondrial | CA5A | unknown | Ki 6.04 |
| Carbonic anhydrase 6 | CA6 | unknown | Ki 5.87 |
| Carbonic anhydrase 2 | CA2 | unknown | Kd 5.56 |
| Carbonic anhydrase 14 | CA14 | unknown | Ki 5.38 |
| Carbonic anhydrase 3 | CA3 | unknown | Ki 4.96 |
| Solute carrier family 12 member 3 | SLC12A3 | inhibitor | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1960-04-07 | FDA | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C03BA04 | CARDIOVASCULAR SYSTEM › DIURETICS › LOW-CEILING DIURETICS, EXCL. THIAZIDES › Sulfonamides, plain |
C03BB04 | CARDIOVASCULAR SYSTEM › DIURETICS › LOW-CEILING DIURETICS, EXCL. THIAZIDES › Sulfonamides and potassium in combination |
C03EA06 | CARDIOVASCULAR 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 term | LLR |
|---|---|
| Hyponatraemia | 442.1 |
| Hypokalaemia | 261.2 |
| Renal artery stenosis | 103.8 |
| Presyncope | 96.1 |
| Lichen planopilaris | 95.7 |
| Renal cyst haemorrhage | 94.5 |
| Renal impairment | 88.8 |
| Meningitis aseptic | 84.7 |
| Acute kidney injury | 81.1 |
| SARS-CoV-2 antibody test positive | 79.7 |
| Abdominal wall haemorrhage | 75.7 |
| Vena cava injury | 75.4 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Chlortalidone is on its molecule page.
| Molecular formula | C14H11ClN2O4S |
|---|---|
| Molecular weight | 338.76 g/mol |
| CAS number | 77-36-1 |
| InChIKey | JIVPVXMEBJLZRO-UHFFFAOYSA-N |
| PubChem CID | 2732 |
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
- DrugCentral drug card 625 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1055 — compound record and bioactivity
- PubChem CID 2732 — chemical identifiers
- DrugBank DB00310 — drug record
- FDA UNII Q0MQD1073Q — substance identity
- DailyMed: FDA labels for Chlortalidone — current prescribing information (label search)
- UniProt P43166 (CA7) — target protein
- UniProt O43570 (CA12) — target protein
- UniProt Q9Y2D0 (CA5B) — target protein
- UniProt Q16790 (CA9) — target protein
- UniProt P22748 (CA4) — target protein
- UniProt P00915 (CA1) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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