Succinylcholine chloride dihydrateProduct ingredient for Succinylcholine

Name
Succinylcholine chloride dihydrate
Drug Entry
Succinylcholine

Succinylcholine is a depolarizing skeletal muscle relaxant consisting of two molecules of the endogenous neurotransmitter acetylcholine (ACh) linked by their acetyl groups.2 It has been widely used for over 50 years,1 most commonly in its chloride salt form, as a means of neuromuscular blockade during intubation and surgical procedures. Its rapid onset and offset, with effects beginning within 60 seconds of intravenous administration and lasting between four to six minutes, make succinylcholine particularly useful in the setting of short medical procedures requiring brief periods of muscle relaxation.9

Accession Number
DBSALT003046
Structure
Synonyms
Succinylcholine chloride dihydrate / Suxamethonium chloride dihydrate / Suxamethonium chloride hydrate
UNII
8L0S1G435E
CAS Number
6101-15-1
Weight
Average: 397.33
Monoisotopic: 396.1793922
Chemical Formula
C14H34Cl2N2O6
InChI Key
FFSBEIRFVXGRPR-UHFFFAOYSA-L
InChI
InChI=1S/C14H30N2O4.2ClH.2H2O/c1-15(2,3)9-11-19-13(17)7-8-14(18)20-12-10-16(4,5)6;;;;/h7-12H2,1-6H3;2*1H;2*1H2/q+2;;;;/p-2
IUPAC Name
trimethyl[2-({4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoyl}oxy)ethyl]azanium dihydrate dichloride
SMILES
O.O.[Cl-].[Cl-].C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C
ChemSpider
571132
ChEBI
61225
Predicted Properties
PropertyValueSource
Water Solubility0.000757 mg/mLALOGPS
logP-2.5ALOGPS
logP-8.4Chemaxon
logS-5.7ALOGPS
pKa (Strongest Basic)-6.8Chemaxon
Physiological Charge2Chemaxon
Hydrogen Acceptor Count2Chemaxon
Hydrogen Donor Count0Chemaxon
Polar Surface Area52.6 Å2Chemaxon
Rotatable Bond Count11Chemaxon
Refractivity100.94 m3·mol-1Chemaxon
Polarizability33.73 Å3Chemaxon
Number of Rings0Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon