Thioridazine
Phenothiazine — NERVOUS SYSTEM
Also known as: dl-Thioridazine, malloryl, meleril, thioridazin, thioridazine HCl, thioridazine hydrochloride
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Thioridazine is an ofp drug in the Phenothiazine class catalogued in DrugCentral. It was first approved by the FDA in 1962. DrugCentral lists 61 molecular targets, including Chrm1|Chrm3|Chrm4|Chrm5|Chrm2, ADRA1D and ADRA1B. Recorded indications include Treatment-Resistant Schizophrenia.
- Approval status: ofp (first approved 1962 by the FDA).
- Drug class: Phenothiazine.
- Molecular targets: Chrm1|Chrm3|Chrm4|Chrm5|Chrm2, ADRA1D, ADRA1B and Adra1b (61 listed in DrugCentral).
- Indications: Treatment-Resistant Schizophrenia.
- ATC code: N05AC02 (Phenothiazines with piperidine structure).
- Molecular formula: C21H26N2S2; molecular weight 370.57 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Treatment-Resistant Schizophrenia
Contraindications (14)
- Breastfeeding (mother)
- Coma
- Congenital long QT syndrome
- Disease of blood AND/OR blood-forming organ
- Epilepsy
- Hyperkalemia
- Hypokalemia
- Neuroleptic malignant syndrome
- Orthostatic hypotension
- Predisposed to Torsades de Pointes Cardiac Arrhythmias
- Prolonged QT interval
- Senile dementia
- Stupor
- Tardive dyskinesia
Mechanism & targets
| Established pharmacologic class | Phenothiazine |
|---|
Molecular targets (61)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Muscarinic acetylcholine receptor | Chrm1|Chrm3|Chrm4|Chrm5|Chrm2 | unknown | IC50 8.70 |
| Alpha-1D adrenergic receptor | ADRA1D | unknown | Ki 8.69 |
| Alpha-1B adrenergic receptor | ADRA1B | unknown | Ki 8.62 |
| Alpha-1B adrenergic receptor | Adra1b | unknown | Ki 8.59 |
| Muscarinic acetylcholine receptor M1 | CHRM1 | unknown | Ki 8.57 |
| D(2) dopamine receptor | Drd2 | unknown | IC50 8.55 |
| Alpha-1A adrenergic receptor | Adra1a | unknown | IC50 8.29 |
| 5-hydroxytryptamine receptor 6 | Htr6 | antagonist | Ki 8.20 |
| Muscarinic acetylcholine receptor M4 | CHRM4 | unknown | Ki 8.05 |
| 5-hydroxytryptamine receptor 2A | HTR2A | antagonist | EC50 8.00 |
| D(4) dopamine receptor | DRD4 | antagonist | Ki 7.98 |
| Alpha-1A adrenergic receptor | ADRA1A | unknown | IC50 7.90 |
| Muscarinic acetylcholine receptor M5 | CHRM5 | unknown | Ki 7.89 |
| Muscarinic acetylcholine receptor M2 | CHRM2 | unknown | Ki 7.85 |
| D(1A) dopamine receptor | Drd1 | unknown | IC50 7.76 |
| Serotonin 2 (5-HT2) receptor | Htr2c|Htr2a|Htr2b | unknown | IC50 7.74 |
| Histamine H1 receptor | HRH1 | antagonist | Ki 7.70 |
| Muscarinic acetylcholine receptor M3 | CHRM3 | unknown | Ki 7.59 |
| D(2) dopamine receptor | DRD2 | antagonist | IC50 7.40 |
| D(3) dopamine receptor | DRD3 | antagonist | IC50 7.30 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1962-03-15 | FDA | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
N05AC02 | NERVOUS SYSTEM › PSYCHOLEPTICS › ANTIPSYCHOTICS › Phenothiazines with piperidine structure |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- FDA label: CYP2D6 · Actionable PGx
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 |
|---|---|
| Antipsychotic drug level below therapeutic | 857.3 |
| Disinhibition | 810.6 |
| Therapeutic product effect variable | 787.6 |
| Obsessive-compulsive disorder | 747.8 |
| Euphoric mood | 701.0 |
| Akathisia | 647.9 |
| Increased appetite | 625.9 |
| Suicide attempt | 393.7 |
| Leukaemia | 348.6 |
| Leukopenia | 305.2 |
| Dyslipidaemia | 291.3 |
| Therapeutic product effect incomplete | 266.2 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Thioridazine is on its molecule page.
| Molecular formula | C21H26N2S2 |
|---|---|
| Molecular weight | 370.57 g/mol |
| CAS number | 50-52-2 |
| InChIKey | KLBQZWRITKRQQV-UHFFFAOYSA-N |
| PubChem CID | 5452 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Thioridazine used for?
DrugCentral lists the following indications for Thioridazine: Treatment-Resistant Schizophrenia.
How does Thioridazine work?
Its molecular targets in DrugCentral include Chrm1|Chrm3|Chrm4|Chrm5|Chrm2, ADRA1D, ADRA1B and Adra1b.
When was Thioridazine first approved?
Thioridazine was first approved by the FDA in 1962.
What drug class does Thioridazine belong to?
Thioridazine is in the Phenothiazine class.
What is the chemical formula of Thioridazine?
Thioridazine has the molecular formula C21H26N2S2 and a molecular weight of 370.57 g/mol.
Browse: all drugs starting with T · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2637 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1200916 — compound record and bioactivity
- PubChem CID 5452 — chemical identifiers
- DrugBank DB00679 — drug record
- FDA UNII N3D6TG58NI — substance identity
- DailyMed: FDA labels for Thioridazine — current prescribing information (label search)
- UniProt P25100 (ADRA1D) — target protein
- UniProt P35368 (ADRA1B) — target protein
- UniProt P11229 (CHRM1) — target protein
- UniProt P08173 (CHRM4) — target protein
- UniProt P28223 (HTR2A) — target protein
- UniProt P21917 (DRD4) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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.