Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H30N2O4.2Cl.2H2O |
Molecular Weight | 397.336 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.[Cl-].[Cl-].C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C
InChI
InChIKey=FFSBEIRFVXGRPR-UHFFFAOYSA-L
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
Succinylcholine also known as suxamethonium is a quaternary skeletal muscle relaxant usually used in the form of its halogen salt. It is is indicated under brand name anectine as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Succinylcholine activates the muscle-type nicotinic acetylcholine receptor followed by desensitization. Succinylcholine does not inhibit the presynaptic alpha3beta2 autoreceptor at clinically relevant concentrations, that provides a possible mechanistic explanation for the typical lack of tetanic fade in succinylcholine-induced neuromuscular blockade. Finally, was explored, that cardiovascular side effects (e.g., tachyarrhythmias) of succinylcholine were not mediated via direct activation of the autonomic ganglionic alpha3beta4 subtype because succinylcholine didn’t not activate the neuronal nicotinic acetylcholine receptor (nAChR) subtypes.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2362997 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16571968 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Palliative | ANECTINE Approved UseSuccinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Launch Date1952 |
AUC
Value | Dose | Co-administered | Analyte | Population |
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18.5 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14564614/ |
1 mg/kg bw single, intravenous dose: 1 mg/kg bw route of administration: Intravenous experiment type: SINGLE co-administered: |
SUCCINYLCHOLINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
58.6 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14564614/ |
2 mg/kg bw single, intravenous dose: 2 mg/kg bw route of administration: Intravenous experiment type: SINGLE co-administered: |
SUCCINYLCHOLINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
25.4 s EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14564614/ |
1 mg/kg bw single, intravenous dose: 1 mg/kg bw route of administration: Intravenous experiment type: SINGLE co-administered: |
SUCCINYLCHOLINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
26.3 s EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/14564614/ |
2 mg/kg bw single, intravenous dose: 2 mg/kg bw route of administration: Intravenous experiment type: SINGLE co-administered: |
SUCCINYLCHOLINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
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1.5 mg/kg single, intravenous Higher than recommended Dose: 1.5 mg/kg Route: intravenous Route: single Dose: 1.5 mg/kg Sources: Page: p.866 |
healthy, 31 n = 22 Health Status: healthy Condition: General anesthesia Age Group: 31 Sex: F Population Size: 22 Sources: Page: p.866 |
|
1.1 mg/kg single, intravenous (max) Recommended Dose: 1.1 mg/kg Route: intravenous Route: single Dose: 1.1 mg/kg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: General anesthesia|Skeletal muscle relaxation Sources: Page: p.1 |
Disc. AE: Rhabdomyolysis, Ventricular arrhythmia... AEs leading to discontinuation/dose reduction: Rhabdomyolysis (acute, rare) Sources: Page: p.1Ventricular arrhythmia (rare) Cardiac arrest (grade 5, rare) |
AEs
AE | Significance | Dose | Population |
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Rhabdomyolysis | acute, rare Disc. AE |
1.1 mg/kg single, intravenous (max) Recommended Dose: 1.1 mg/kg Route: intravenous Route: single Dose: 1.1 mg/kg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: General anesthesia|Skeletal muscle relaxation Sources: Page: p.1 |
Cardiac arrest | grade 5, rare Disc. AE |
1.1 mg/kg single, intravenous (max) Recommended Dose: 1.1 mg/kg Route: intravenous Route: single Dose: 1.1 mg/kg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: General anesthesia|Skeletal muscle relaxation Sources: Page: p.1 |
Ventricular arrhythmia | rare Disc. AE |
1.1 mg/kg single, intravenous (max) Recommended Dose: 1.1 mg/kg Route: intravenous Route: single Dose: 1.1 mg/kg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: General anesthesia|Skeletal muscle relaxation Sources: Page: p.1 |
PubMed
Title | Date | PubMed |
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Cardiac arrest related to anesthesia. Contributing factors in infants and children. | 1975 Jul 21 |
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Hypersensitivity to suxamethonium in a Suffolk family. | 1976 Jul |
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Continuous propofol administration for suxamethonium-induced postoperative myalgia. | 1999 May |
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Is succinylcholine after pretreatment with d-tubocurarine and lidocaine contraindicated for outpatient anesthesia? | 2000 Aug |
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Interactions of neuromuscular blocking drugs. | 2001 |
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Choice of the muscle relaxant for rapid-sequence induction. | 2001 |
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Choice of the hypnotic and the opioid for rapid-sequence induction. | 2001 |
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Difficult airway management of a child impaled through the neck. | 2001 |
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Newer neuromuscular blocking agents: how do they compare with established agents? | 2001 |
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A comparison of the effects of sarin and succinylcholine on respiratory parameters in anesthetized domestic swine. | 2001 Apr |
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Giant multimodal heart motoneurons of Achatina fulica: a new cardioregulatory input in pulmonates. | 2001 Aug |
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Effects of combined methohexitone-remifentanil anaesthesia in electroconvulsive therapy. | 2001 Aug |
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Why do we still use suxamethonium for caesarean section? | 2001 Dec |
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Analysis of mutations in the plasma cholinesterase gene of patients with a history of prolonged neuromuscular block during anesthesia. | 2001 Dec |
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The laryngeal mask airway is effective (and probably safe) in selected healthy parturients for elective Cesarean section: a prospective study of 1067 cases. | 2001 Dec |
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Intubating trauma patients before reaching hospital -- revisited. | 2001 Dec |
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A randomized multicenter study of remifentanil compared with halothane in neonates and infants undergoing pyloromyotomy. I. Emergence and recovery profiles. | 2001 Dec |
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Neuromuscular blockers in surgery and intensive care, Part 2. | 2001 Dec 15 |
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B-lymphocytes from malignant hyperthermia-susceptible patients have an increased sensitivity to skeletal muscle ryanodine receptor activators. | 2001 Dec 21 |
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Second dose thiopentone attenuates the haemodynamic response to laryngoscopy and intubation. | 2001 Feb |
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Sore throat following tracheal intubation. | 2001 Feb |
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Anaesthesia and myotonia--an Australian experience. | 2001 Feb |
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The use of esmolol as an alternative to remifentanil during desflurane anesthesia for fast-track outpatient gynecologic laparoscopic surgery. | 2001 Feb |
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An evaluation of Automode, a computer-controlled ventilator mode, with the Siemens Servo 300A ventilator, using a porcine model. | 2001 Jan |
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Unplanned administration of atropine, succinylcholine and lidocaine. | 2001 Jan |
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Effectiveness of continuous positive airway pressure to enhance pre-oxygenation in morbidly obese women. | 2001 Jul |
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Frequency of haemoglobin desaturation with the use of succinylcholine during rapid sequence induction of anaesthesia. | 2001 Jul |
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Asystole during electroconvulsive therapy: a case report. | 2001 Jun |
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Succinylcholine pretreatment using gallamine or mivacurium during rapid sequence induction in children: a randomized, controlled study. | 2001 Jun |
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[Short-term anesthesia to stop persistent hiccups]. | 2001 Jun 22 |
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Conquer difficult airways. Strategies to help you identify & control a problem airway. | 2001 Mar |
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Hemoglobin desaturation after succinylcholine-induced apnea: a study of the recovery of spontaneous ventilation in healthy volunteers. | 2001 May |
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The intubating laryngeal mask airway after induction of general anesthesia versus awake fiberoptic intubation in patients with difficult airways. | 2001 May |
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Rapacuronium: an alternative to succinylcholine for electroconvulsive therapy. | 2001 May |
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[Pseudocholinesterase (ChE)]. | 2001 Nov |
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Retrospective analysis of drug-induced urticaria and angioedema: a survey of 2287 patients. | 2001 Nov |
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Is succinylcholine appropriate or obsolete in the intensive care unit? | 2001 Oct |
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Goal oriented general anesthesia for Cesarean section in a parturient with a large intracranial epidermoid cyst. | 2001 Oct |
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Intramuscular succinylcholine and laryngospasm. | 2001 Oct |
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[Anesthesia for electroconvulsive therapy during pregnancy--a case report]. | 2001 Sep |
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Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne muscular dystrophy following general anaesthesia. | 2001 Sep |
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Autosomal dominant canine malignant hyperthermia is caused by a mutation in the gene encoding the skeletal muscle calcium release channel (RYR1). | 2001 Sep |
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Different patterns of mast cell activation by muscle relaxants in human skin. | 2001 Sep |
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Succinylcholine in the intensive care unit. | 2002 Jan |
Patents
Sample Use Guides
Adults: For Short Surgical Procedures: the average dose required to produce neuromuscular blockade and to facilitate tracheal intubation is 0.6 mg/kg ANECTINE (Succinylcholine Chloride Injection) given intravenously. The optimum dose will vary among individuals and may be from 0.3 to 1.1 mg/kg for adults. Following administration of doses in this range, neuromuscular blockade develops in about 1 minute; maximum blockade may persist for about 2 minutes, after which recovery takes place within 4 to 6 minutes. However, very large doses may result in more prolonged blockade. A 5- to 10-mg test dose may be used to determine the sensitivity of the patient and the individual recovery time (see PRECAUTIONS). For Long Surgical Procedures The dose of succinylcholine administered by infusion depends upon the duration of the surgical procedure and the need for muscle relaxation. The average rate for an adult ranges between 2.5 and 4.3 mg per minute. Solutions containing from 1 to 2 mg per mL succinylcholine have commonly been used for continuous infusion. The more dilute solution (1 mg per mL) is probably preferable from the standpoint of ease of control of the rate of administration of the drug and, hence, of relaxation. This IV solution containing 1 mg per mL may be administered at a rate of 0.5 mg (0.5 mL) to 10 mg (10 mL) per minute to obtain the required amount of relaxation. Intermittent IV injections of succinylcholine may also be used to provide muscle relaxation for long procedures. An IV injection of 0.3 to 1.1 mg/kg may be given initially, followed, at appropriate intervals, by further injections of 0.04 to 0.07 mg/kg to maintain the degree of relaxation required.
Pediatrics: for emergency tracheal intubation or in instances where immediate securing of the airway is necessary, the IV dose of succinylcholine is 2 mg/kg for infants and small children; for older children and adolescents the dose is 1 mg/kg. Rarely, IV bolus administration of succinylcholine in infants and children may result in malignant ventricular arrhythmias and cardiac arrest secondary to acute rhabdomyolysis with hyperkalemia. In such situations, an underlying myopathy should be suspected. Intravenous bolus administration of succinylcholine in infants or children may result in profound bradycardia or, rarely, asystole. As in adults, the incidence of bradycardia in children is higher
Intramuscular Use: If necessary, succinylcholine may be given intramuscularly to infants, older children, or adults when a suitable vein is inaccessible. A dose of up to 3 to 4 mg/kg may be given, but not more than 150 mg total dose should be administered by this route. The onset of effect of succinylcholine given intramuscularly is usually observed in about 2 to 3 minutes.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3790394
The rat diaphragm was used as an in vitro model for studies of contractures synergistically-induced by halothane and suxamethonium (succinylcholine). The effects of three agents reported to inhibit phospholipase A2 activity (quinacrine, spermine and indomethacin), tubocurarine and dantrolene were examined on these contractures. Contractures induced by 1% halothane (0.26 +/- 0.02 g) (mean +/- SEM) were increased (0.60 +/- 0.04 g) if suxamethonium 50 mmol litre-1 was also in the bathing medium. Suxamethonium-induced contractures (0.22 +/- 0.03 g) were also enhanced when halothane was present (0.51 +/- 0.03 g). Spermine, indomethacin and dantrolene antagonized both halothane- and suxamethonium-induced contractures. Quinacrine potentiated contractures induced by either halothane or suxamethonium. Contractures induced by suxamethonium were antagonized by tubocurarine; however, contractures induced by halothane were not antagonized by tubocurarine. These results suggest that free fatty acids may be involved in contractures induced synergistically by halothane and suxamethonium. Different mechanisms are involved in the induction of contractures by suxamethonium than by halothane.
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SUB71135
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SUCCINYLCHOLINE CHLORIDE DIHYDRATE
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PRIMARY | Description: A white or almost white, crystalline powder; odourless or almost odourless. Solubility: Soluble in 1 pan of water; slightly soluble in ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Muscle relaxant. Storage: Suxamethonium chloride should be kept in a tightly closed container, protected from light. Additional information: Suxamethonium chloride is hygroscopic. Even in the absence of light, it is gradually degraded on exposure to a humid atmosphere, the decomposition being faster at higher temperatures. Definition: Suxamethonium chloride contains not less than 98.0% and not more than 101.0% of C14H30Cl2N2O4, calculated with reference to the anhydrous substance. | ||
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2397714
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61225
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100000135573
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ACTIVE MOIETY
SUBSTANCE RECORD