Basic information
- CAS
302-83-0- Standard SMILES
CC[N+](C)(C)c1cccc(O)c1.[Br-]- InChIKey
CAEPIUXAUPYIIJ-UHFFFAOYSA-N- Molecular formula
- C10H16BrNO
- Average molar mass
- 246.14 g/mol
- Monoisotopic mass
- 245.04153
Names & identifiers
- Preferred name
- Benzenaminium, N-ethyl-3-hydroxy-N,N-dimethyl-, bromide (1:1)
- IUPAC
- ethyl-(3-hydroxyphenyl)-dimethylazanium bromide
Names & synonyms
Edrophonium bromide302-83-0Tensilon bromideKX008093VWBromide, EdrophoniumBENZENAMINIUM, N-ETHYL-3-HYDROXY-N,N-DIMETHYL-, BROMIDE (1:1)RefChem:136306N-Ethyl-3-hydroxy-N,N-dimethylbenzenaminium bromideOedrophaniumethyl-(3-hydroxyphenyl)-dimethylazanium;bromideAMMONIUM,(3-HYDROXYPHENYL)DIMETHYLETHYL-,BROMIDEedrophone bromide
Show more names
Ro 2-3198UNII-KX008093VW3-Hydroxyphenyldimethylethylammonium bromideEthyl(m-hydroxyphenyl)dimethylammonium bromideAmmonium, ethyl(m-hydroxyphenyl)dimethyl-, bromideCHEMBL60745SCHEMBL2462104Benzenaminium, N-ethyl-3-hydroxy-N,N-dimethyl-, bromide
Database identifiers
- CAS
302-83-0- PubChem CID
- 9336
- ChEMBL
CHEMBL60745- UNII
- KX008093VW
Properties
Computed structural properties
- Topological polar surface area
- 20.2 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 2
- Heavy atoms
- 13
- Formal charge
- 0
- Complexity
- 145
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Agents counteracting or neutralizing the action of POISONS.
Drugs that inhibit cholinesterases. The neurotransmitter ACETYLCHOLINE is rapidly hydrolyzed, and thereby inactivated, by cholinesterases. When cholinesterases are inhibited, the action of endogenously released acetylcholine at cholinergic synapses is potentiated. Cholinesterase inhibitors are widely used clinically for their potentiation of cholinergic inputs to the gastrointestinal tract and urinary bladder, the eye, and skeletal muscles; they are also used for their effects on the heart and the central nervous system.
Related reactions
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Compound notes
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