Butylscopolamine
drug drugOn this page
Also known as N-butylscopolammoniumN-butylscopolammonium cationN-butylscopolammonium ionBUTYLSCOPOLAMINE BROMIDEscopolamine butylbromide
Summary
Butylscopolamine (CHEMBL1618102) is an approved small-molecule muscarinic antagonist (ATC A03BB01); indicated across 2 conditions.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: A03BB01
- Indications: 2 conditions
- Clinical trials: 1
- Chemistry: 360.5 Da · C21H30NO4+
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1618102 |
| Name | Butylscopolamine |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | yes |
| PubChem CID | 160883 |
| ChEBI | CHEBI:145701 |
| ATC | A03BB01 |
| Molecular formula | C21H30NO4+ |
| Molecular weight | 360.5 |
| InChIKey | YBCNXCRZPWQOBR-MWGADRMYSA-N |
SMILES: CCCC[N+]1([C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)OC(=O)[C@H](CO)C4=CC=CC=C4)C
IUPAC name: [(1R,2R,4S,5S)-9-butyl-9-methyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate
ChEBI definition: A carboxylic ester resulting from the formal condensation of the carboxy group of (2S)-3-hydroxy-2-phenylpropanoic acid with the hydroxy group of (2R,4S,5S,7s)-9-butyl-7-hydroxy-9-methyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane.
Pharmacological roles (ChEBI): muscarinic antagonist, antispasmodic drug.
Also known as: Butylscopolamine, N-butylscopolammonium, N-butylscopolammonium cation, N-butylscopolammonium ion, BUTYLSCOPOLAMINE, BUTYLSCOPOLAMINE BROMIDE, scopolamine butylbromide
Parent form; salt/anhydrous children: CHEMBL1256901
Patent coverage: 5 distinct patent families (6 SureChEMBL compound mentions), from 1 matched compound structure(s). 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: 3 (assay-derived). Sample: Muscarinic acetylcholine receptor M2, Muscarinic acetylcholine receptor M1, Voltage-gated inwardly rectifying potassium channel KCNH2.
Bioactivity
ChEMBL activities: 3 potent at pChembl ≥ 5 of 3 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| CHRM2 | 6.44 | AC50 | 365.5 | nM | CHEMBL_ACT_25195802 |
| KCNH2 | 5.55 | AC50 | 2800 | nM | CHEMBL_ACT_25117749 |
| CHRM1 | 5.33 | AC50 | 4724 | nM | CHEMBL_ACT_25210270 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indication records carry no mapped disease name (EFO/MeSH-only); none shown.
Clinical trials
Total trials: 1.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03961165 | PHASE3 | COMPLETED | BUSCLAB - Buscopan to Prevent Slow Progress in Labor |
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
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.