Succinylcholine Bromide
Basic information
- CAS
55-94-7- Standard SMILES
C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C.[Br-].[Br-]- InChIKey
HKDOIORVQFUBKO-UHFFFAOYSA-L- Molecular formula
- C14H30Br2N2O4
- Average molar mass
- 450.21 g/mol
- Monoisotopic mass
- 448.05723
Names & identifiers
- Preferred name
- Succinylcholine Bromide
- IUPAC
- trimethyl-[2-[4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoyl]oxyethyl]azanium dibromide
Names & synonyms
Suxamethonium bromideSuccinylcholine bromide1MBL83KX8JNSC-151059DTXSID30877661RefChem:186862DTXCID101015732200-248-155-94-7MyorelaxinBrevidil MSuxamethonium dibromide
Show more names
L.T. 12,2'-Succinyldioxybis(ethyltrimethylammonium) dibromideM & B 2207Brevedil MBis(2-dimethylaminoethyl)succinate bis(methobromide)370 I.S.2,2'-(succinylbis(oxy))bis(N,N,N-trimethylethan-1-aminium) bromidetrimethyl-[2-[4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoyl]oxyethyl]azanium;dibromide
Database identifiers
- CAS
55-94-7- PubChem CID
- 66129
- DTXSID
DTXSID30877661- ChEMBL
CHEMBL2104486- UNII
- 1MBL83KX8J
- EC Number
- 200-248-1
Properties
Computed structural properties
- Topological polar surface area
- 52.6 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 11
- Heavy atoms
- 22
- Formal charge
- 0
- Complexity
- 284
Chemistry & industry
Pharmacology
MeSH Pharmacological ClassificationDrugs that interrupt transmission at the skeletal neuromuscular junction by causing sustained depolarization of the motor end plate. These agents are primarily used as adjuvants in surgical anesthesia to cause skeletal muscle relaxation.
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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