CHEBI:45652 - succinylcholine

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ChEBI Name succinylcholine
Definition A quaternary ammonium ion that is the bis-choline ester of succinic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:45650, CHEBI:133060, CHEBI:9311
Supplier Information
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Formula C14H30N2O4
Net Charge +2
Average Mass 290.39908
Monoisotopic Mass 290.21946
InChI InChI=1S/C14H30N2O4/c1-15(2,3)9-11-19-13(17)7-8-14(18)20-12-10-16(4,5)6/h7-12H2,1-6H3/q+2
Roles Classification
Biological Role(s): drug allergen
Any drug which causes the onset of an allergic reaction.
Application(s): muscle relaxant
A drug used to produce muscle relaxation (excepting neuromuscular blocking agents). Its primary clinical and therapeutic use is the treatment of muscle spasm and immobility associated with strains, sprains, and injuries of the back and, to a lesser degree, injuries to the neck. Also used for the treatment of a variety of clinical conditions that have in common only the presence of skeletal muscle hyperactivity, for example, the muscle spasms that can occur in multiple sclerosis.
drug allergen
Any drug which causes the onset of an allergic reaction.
neuromuscular agent
A drug used for its actions on skeletal muscle.
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ChEBI Ontology
Outgoing succinylcholine (CHEBI:45652) has role drug allergen (CHEBI:88188)
succinylcholine (CHEBI:45652) has role muscle relaxant (CHEBI:51371)
succinylcholine (CHEBI:45652) has role neuromuscular agent (CHEBI:51372)
succinylcholine (CHEBI:45652) is a quaternary ammonium ion (CHEBI:35267)
succinylcholine (CHEBI:45652) is a succinate ester (CHEBI:36181)
Incoming succinylcholine chloride (anhydrous) (CHEBI:61219) has part succinylcholine (CHEBI:45652)
Synonyms Sources
Dicholine succinate ChemIDplus
succinic acid, diester with choline Deprecated term ChemIDplus
Succinocholine ChemIDplus
Succinoylcholine ChemIDplus
Succinylbischoline ChEBI
Succinylcholine KEGG COMPOUND
Succinyldicholine ChEBI
suxamethonium ChemIDplus
Suxamethonium KEGG COMPOUND
Manual Xrefs Databases
2489 DrugCentral
DB00202 DrugBank
HMDB0014347 HMDB
View more database links
Registry Numbers Types Sources
1805311 Reaxys Registry Number Reaxys
1805311 Beilstein Registry Number Beilstein
306-40-1 CAS Registry Number NIST Chemistry WebBook
306-40-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11123992 PubMed citation ChEMBL
13063382 PubMed citation Europe PMC
17667569 PubMed citation Europe PMC
23223104 PubMed citation Europe PMC
23838346 PubMed citation Europe PMC
24018151 PubMed citation Europe PMC
29368335 PubMed citation Europe PMC
4032432 PubMed citation ChEMBL
6196640 PubMed citation Europe PMC
7526642 PubMed citation Europe PMC
9435889 PubMed citation ChEMBL
Last Modified
24 April 2018