Quazepam
Benzodiazepine — NERVOUS SYSTEM
Also known as: prosedar, quazium, Sch 16134, Sch-16134
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Quazepam is an ofp drug in the Benzodiazepine class catalogued in DrugCentral. It was first approved by the FDA in 1985. DrugCentral lists 3 molecular targets, including GABRA1|GABRB1|GABRG2, GABRB1|GABRG2|GABRA2 and GABRB1|GABRG2|GABRA3. Recorded indications include Insomnia.
- Approval status: ofp (first approved 1985 by the FDA).
- Drug class: Benzodiazepine.
- Molecular targets: GABRA1|GABRB1|GABRG2, GABRB1|GABRG2|GABRA2 and GABRB1|GABRG2|GABRA3 (3 listed in DrugCentral).
- Indications: Insomnia.
- ATC code: N05CD10 (Benzodiazepine derivatives).
- Molecular formula: C17H11ClF4N2S; molecular weight 386.79 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Insomnia
Contraindications (17)
- Alcohol intoxication
- Breastfeeding (mother)
- Coma
- Decreased respiratory function
- Depressive disorder
- Disease of liver
- Disorder of lung
- Hypoalbuminemia
- Kidney disease
- Porphyria
- Pregnancy, function
- Severe chronic obstructive pulmonary disease
- Shock
- Sleep apnea
- Sleep automatism
- Substance abuse
- Suicidal thoughts
Mechanism & targets
| Established pharmacologic class | Benzodiazepine |
|---|
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| GABA A receptor alpha-1/beta-1/gamma-2 | GABRA1|GABRB1|GABRG2 | positive allosteric modulator | Ki 7.71 |
| GABA A receptor alpha-2/beta-1/gamma-2 | GABRB1|GABRG2|GABRA2 | positive allosteric modulator | Ki 6.69 |
| GABA A receptor alpha-3/beta-1/gamma-2 | GABRB1|GABRG2|GABRA3 | positive allosteric modulator | Ki 6.63 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1985-12-27 | FDA | — | SCIECURE PHARMA INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
N05CD10 | NERVOUS SYSTEM › PSYCHOLEPTICS › HYPNOTICS AND SEDATIVES › Benzodiazepine derivatives |
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 |
|---|---|
| Altered state of consciousness | 97.4 |
| Suicide attempt | 64.7 |
| Intentional overdose | 59.2 |
| Blood creatine phosphokinase increased | 46.6 |
| Salivary hypersecretion | 40.4 |
| Psychiatric symptom | 37.1 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Quazepam is on its molecule page.
| Molecular formula | C17H11ClF4N2S |
|---|---|
| Molecular weight | 386.79 g/mol |
| CAS number | 36735-22-5 |
| InChIKey | IKMPWMZBZSAONZ-UHFFFAOYSA-N |
| PubChem CID | 4999 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Quazepam used for?
DrugCentral lists the following indications for Quazepam: Insomnia.
How does Quazepam work?
Its molecular targets in DrugCentral include GABRA1|GABRB1|GABRG2 (positive allosteric modulator), GABRB1|GABRG2|GABRA2 (positive allosteric modulator) and GABRB1|GABRG2|GABRA3 (positive allosteric modulator).
When was Quazepam first approved?
Quazepam was first approved by the FDA in 1985.
What drug class does Quazepam belong to?
Quazepam is in the Benzodiazepine class.
What is the chemical formula of Quazepam?
Quazepam has the molecular formula C17H11ClF4N2S and a molecular weight of 386.79 g/mol.
Browse: all drugs starting with Q · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2336 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1200472 — compound record and bioactivity
- PubChem CID 4999 — chemical identifiers
- DrugBank DB01589 — drug record
- FDA UNII JF8V0828ZI — substance identity
- DailyMed: FDA labels for Quazepam — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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