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Compound InformationSONAR Target prediction
Name:

Succinylcholine chloride

Unique Identifier:LOPAC 00233
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C14Cl2H32N2O4
Molecular Weight:331.066 g/mol
X log p:0.012  (online calculus)
Lipinksi Failures1
TPSA52.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:4
Rotatable Bond Count:11
Canonical Smiles:[ClH-].[ClH-].C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C
Class:Cholinergic
Action:Antagonist
Selectivity:Nicotinic
Generic_name:Succinylcholine
Chemical_iupac_name:trimethyl-[2-[3-(2-trimethylammonioethoxycarbonyl)propanoyloxy]ethyl]ammonium
Drug_type:Approved Drug
Pharmgkb_id:PA451522
Kegg_compound_id:C07546
Drugbank_id:APRD00159
Cas_registry_number:306-40-1
Drug_category:Neuromuscular Depolarizing Agents; Skeletal Muscle Relaxants; ATC:M03BX
Indication:Used in surgical procedures where a rapid onset and brief duration of muscle
relaxation is needed (includes intubation, endoscopies, and ECT)
Pharmacology:Succinylcholine is indicated as an adjunct to general anesthesia, to facilitate
tracheal intubation, and to provide skeletal muscle relaxation during surgery or
mechanical ventilation. Succinylcholine is a depolarizing skeletal muscle relaxant.
As does acetylcholine, it combines with the cholinergic receptors of the motor end
plate to produce depolarization. This depolarization may be observed as
fasciculations. Subsequent neuromuscular transmission is inhibited so long as
adequate concentration of succinylcholine remains at the receptor site.
Succinylcholine has no direct action on the uterus or other smooth muscle
structures.
Mechanism_of_action:The mechanism of action of Succinylcholine involves what appears to be a
"persistent" depolarization of the neuromuscular junction. This depolarization is
caused by Succinylcholine mimicking the effect of acetylcholine but without being
rapidly hydrolysed by acetylcholinesterase. This depolarization leads to
desensitization.
Organisms_affected:Humans and other mammals

Found: 24 nonactive as graph: single | with analogs 2 3 4 5 6 7 8 9 10  Next >> [24]
Species: 4932
Condition: BY4741
Replicates: 8
Raw OD Value: r im 0.7251±0.0211036
Normalized OD Score: sc h 0.9985±0.0117801
Z-Score: -0.0538±0.371307
p-Value: 0.881184
Z-Factor: -16.0147
Fitness Defect: 0.1265
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Lopac
Plate Number and Position:14|D11
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:27.80 Celcius
Date:2005-04-07 YYYY-MM-DD
Plate CH Control (+):0.047306249999999994±0.00108
Plate DMSO Control (-):0.7395374999999998±0.02629
Plate Z-Factor:0.8745
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DBLink | Rows returned: 142 3 Next >> 
5314 trimethyl-[2-[3-(2-trimethylammonioethoxycarbonyl)propanoyloxy]ethyl]azanium
22475 trimethyl-[2-[3-(2-trimethylammonioethoxycarbonyl)propanoyloxy]ethyl]azanium dichloride
66129 trimethyl-[2-[3-(2-trimethylammonioethoxycarbonyl)propanoyloxy]ethyl]azanium dibromide
68325 trimethyl-[2-[3-(2-trimethylammonioethoxycarbonyl)propanoyloxy]ethyl]azanium diiodide
87986 bis(2-dimethylaminoethyl) butanedioate
116947 4-(2-dimethylaminoethoxy)-4-oxo-butanoic acid

internal high similarity DBLink | Rows returned: 0

active | Cluster 239 | Additional Members: 7 | Rows returned: 2
LOPAC 00736 0.451612903225806
SPE01500104 0.428571428571429

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