Medazepam
drugOn this page
Also known as NobriumPamnaceSID26757942SID144206658
Summary
Medazepam (CHEMBL28333) is an approved small molecule (ATC N05BA03); indicated across 1 condition including anxiety.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: N05BA03
- Indications: 1 condition
- Chemistry: 270.75 Da · C16H15ClN2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL28333 |
| Name | Medazepam |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 4041 |
| ATC | N05BA03 |
| Molecular formula | C16H15ClN2 |
| Molecular weight | 270.75 |
| InChIKey | YLCXGBZIZBEVPZ-UHFFFAOYSA-N |
SMILES: CN1CCN=C(C2=C1C=CC(=C2)Cl)C3=CC=CC=C3
IUPAC name: 7-chloro-1-methyl-5-phenyl-2,3-dihydro-1,4-benzodiazepine
Also known as: Medazepam, Nobrium, Pamnace, SID26757942, SID144206658, MEDAZEPAM, medazepam
Parent form; salt/anhydrous children: CHEMBL2106842
Patent coverage: 2,419 distinct patent families (6,650 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 6,625 (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: 12 (assay-derived). Sample: Neuronal acetylcholine receptor subunit alpha-4, GABA-A receptor; anion channel, 5-hydroxytryptamine receptor 2C, Alpha-1A adrenergic receptor, Prostaglandin G/H synthase 2, Kappa-type opioid receptor, Sodium-dependent dopamine transporter, Adenosine receptor A3, 3’,5’-cyclic-AMP phosphodiesterase 4D, Nuclear receptor subfamily 1 group I member 2.
Bioactivity
ChEMBL activities: 5 potent at pChembl ≥ 5 of 12 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| O09028 | 6.28 | Ki | 528 | nM | CHEMBL_ACT_458157 |
| OPRK1 | 6 | AC50 | 990 | nM | CHEMBL_ACT_25129818 |
| P62813 | 5.68 | AC50 | 2100 | nM | CHEMBL_ACT_25131009 |
| NR1I2 | 5.51 | AC50 | 3100 | nM | CHEMBL_ACT_25188482 |
| PDE4D | 5.28 | AC50 | 5200 | nM | CHEMBL_ACT_25185758 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
1 indication (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 |
|---|---|---|---|
| anxiety | 4 | MONDO:0011918 | EFO:0005230 |
Clinical trials
Total trials: 0.
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: anxiety