Temazepam
drugOn this page
Also known as (rs)-temazepamKentepamNormisonNSC-246303RestorilTemazTemazepam civWY-3917SID29215382SID144205223SID144207242
Summary
Temazepam (CHEMBL967) is an approved small molecule (ATC N05CD07); indicated across 6 conditions including insomnia and chronic obstructive pulmonary disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: N05CD07
- Indications: 6 conditions
- Clinical trials: 6
- Chemistry: 300.74 Da · C16H13ClN2O2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL967 |
| Name | Temazepam |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 5391 |
| ATC | N05CD07 |
| Molecular formula | C16H13ClN2O2 |
| Molecular weight | 300.74 |
| InChIKey | SEQDDYPDSLOBDC-UHFFFAOYSA-N |
SMILES: CN1C2=C(C=C(C=C2)Cl)C(=NC(C1=O)O)C3=CC=CC=C3
IUPAC name: 7-chloro-3-hydroxy-1-methyl-5-phenyl-3H-1,4-benzodiazepin-2-one
Also known as: (rs)-temazepam, Kentepam, Normison, NSC-246303, Restoril, Temaz, Temazepam, Temazepam civ, WY-3917, SID29215382, TEMAZEPAM, temazepam
Patent coverage: 8,496 distinct patent families (25,646 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 25,547 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 4 (assay-derived). Sample: Prelamin-A/C, Kappa-type opioid receptor, cGMP-inhibited 3’,5’-cyclic phosphodiesterase 3A, Gamma-aminobutyric acid receptor subunit alpha-1.
Bioactivity
ChEMBL activities: 4 potent at pChembl ≥ 5 of 4 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P62813 | 7.36 | AC50 | 44 | nM | CHEMBL_ACT_25130811 |
| LMNA | 6.55 | Potency | 281.8 | nM | CHEMBL_ACT_3621546 |
| PDE3A | 5.52 | AC50 | 3000 | nM | CHEMBL_ACT_25190911 |
| OPRK1 | 5.04 | AC50 | 9191 | nM | CHEMBL_ACT_25129630 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
6 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| insomnia | 4 | MONDO:0013600 | EFO:0004698 |
| chronic obstructive pulmonary disease | 3 | MONDO:0005002 | EFO:0000341 |
| anxiety | 3 | MONDO:0011918 | EFO:0005230 |
| dementia | 3 | MONDO:0001627 | HP:0000726 |
| depressive disorder | 3 | MONDO:0002050 | MONDO:0002050 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 2 |
| PHASE3 | 2 |
| PHASE1 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00465972 | PHASE4 | COMPLETED | The Treatment of Insomnia in Patients With HIV Disease |
| NCT02153788 | PHASE4 | COMPLETED | Efficacy and Safety of Temazepam in HIV Seropositive Patients With Insomnia |
| NCT00245661 | PHASE3 | COMPLETED | Effects of Temazepam in Patients With Chronic Pulmonary Obstructive Disease |
| NCT02374567 | PHASE3 | TERMINATED | Pharmacovigilance in Gerontopsychiatric Patients |
| NCT00940550 | PHASE1 | COMPLETED | Study to Investigate the Effects of Melatonin, Temazepam & Zolpidem on Sleep EEG in Men and Women |
| NCT01519544 | Not specified | COMPLETED | Comparison of Temazepam and Acetazolamide to Treat Difficulty Sleeping at High Altitude |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).