EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C23H31N2O.I |
| Net Charge | 0 |
| Average Mass | 478.418 |
| Monoisotopic Mass | 478.14811 |
| SMILES | C[N+]1(CCC(C(N)=O)(c2ccccc2)c2ccccc2)CCCCCC1.[I-] |
| InChI | InChI=1S/C23H30N2O.HI/c1-25(17-10-2-3-11-18-25)19-16-23(22(24)26,20-12-6-4-7-13-20)21-14-8-5-9-15-21;/h4-9,12-15H,2-3,10-11,16-19H2,1H3,(H-,24,26);1H |
| InChIKey | HMFBCJNMIYZRKQ-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Biological Role: | cholinergic antagonist Any drug that binds to but does not activate cholinergic receptors, thereby blocking the actions of acetylcholine or cholinergic agonists. |
| Applications: | antispasmodic drug A drug that suppresses spasms. These are usually caused by smooth muscle contraction, especially in tubular organs. The effect is to prevent spasms of the stomach, intestine or urinary bladder. cholinergic antagonist Any drug that binds to but does not activate cholinergic receptors, thereby blocking the actions of acetylcholine or cholinergic agonists. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| buzepide metiodide (CHEBI:135429) has part buzepide(1+) (CHEBI:157622) |
| buzepide metiodide (CHEBI:135429) has role antispasmodic drug (CHEBI:53784) |
| buzepide metiodide (CHEBI:135429) has role cholinergic antagonist (CHEBI:48873) |
| buzepide metiodide (CHEBI:135429) is a organic iodide salt (CHEBI:50356) |
| IUPAC Name |
|---|
| 1-(4-amino-4-oxo-3,3-diphenylbutyl)-1-methylazepanium iodide |
| INNs | Source |
|---|---|
| buzepide metiodide | WHO MedNet |
| buzepidi metiodidum | WHO MedNet |
| métiodure de buzépide | WHO MedNet |
| metioduro de buzepida | WHO MedNet |
| Synonyms | Source |
|---|---|
| 1-(3-carbamoyl-3,3-diphenylpropyl)-1-methylazepan-1-ium iodide | ChEBI |
| 1-(3-carbamoyl-3,3-diphenylpropyl)hexahydro-1-methylazepinium iodide | ChEBI |
| 1-(4-amino-4-oxo-3,3-diphenylbutyl)-1-methylazepan-1-ium iodide | IUPAC |
| buzepide methiodide | ChemIDplus |
| difexamide methiodide | DrugCentral |
| diphexamide iodomethylate | DrugCentral |
| Manual Xrefs | Databases |
|---|---|
| 459 | DrugCentral |
| Registry Numbers | Sources |
|---|---|
| CAS:15351-05-0 | ChemIDplus |
| Citations |
|---|