Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C37H61N2O4.Br |
Molecular Weight | 677.795 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Br-].[H][C@@]12C[C@@H]([C@H](OC(=O)CC)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])C[C@H](OC(C)=O)[C@H](C[C@]34C)N5CCCCC5)[N+]6(CC=C)CCCCC6
InChI
InChIKey=LVQTUXZKLGXYIU-GWSNJHLMSA-M
InChI=1S/C37H61N2O4.BrH/c1-6-20-39(21-12-9-13-22-39)32-24-30-28-15-14-27-23-33(42-26(3)40)31(38-18-10-8-11-19-38)25-37(27,5)29(28)16-17-36(30,4)35(32)43-34(41)7-2;/h6,27-33,35H,1,7-25H2,2-5H3;1H/q+1;/p-1/t27-,28+,29-,30-,31-,32-,33-,35-,36-,37-;/m0./s1
Molecular Formula | BrH |
Molecular Weight | 80.912 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C37H61N2O4 |
Molecular Weight | 597.8912 |
Charge | 1 |
Count |
|
Stereochemistry | EPIMERIC |
Additional Stereochemistry | No |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionCurator's Comment: description was created based on several sources, including:
http://www.rxlist.com/raplon-drug.htm | https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=43578
Curator's Comment: description was created based on several sources, including:
http://www.rxlist.com/raplon-drug.htm | https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=43578
Rapacuronium bromide (RAPLON), a nondepolarizing neuromuscular blocking agent, is a negative allosteric modulator of muscarinic acetylcholine receptors. Rapacuronium bromide is indicated as an adjunct to general anesthesia to facilitate tracheal intubation and to provide skeletal muscle relaxation during surgical procedures. There were no specific pharmacokinetic studies conducted to examine the drug-drug interactions of RAPLON. Due to the risk of fatal bronchospasm, it was withdrawn from the United States market less than 2 years after its FDA approval.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL216 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20038295 |
4.3 null [pEC50] | ||
4.55 null [pEC50] | |||
4.12 null [pEC50] | |||
Target ID: CHEMBL1821 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20038295 |
9.69 null [pEC50] | ||
Target ID: CHEMBL2035 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20038295 |
4.21 null [pEC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | RAPLON Approved UseRAPLON™ (rapacuronium bromide) for Injection is indicated as an adjunct to general anesthesia to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgical procedures. Launch Date1999 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
7 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10500937/ |
0.6 mg/kg single, intravenous dose: 0.6 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
RAPACURONIUM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
160 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10500937/ |
0.6 mg/kg single, intravenous dose: 0.6 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
RAPACURONIUM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
70.3 min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10500937/ |
0.6 mg/kg single, intravenous dose: 0.6 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
RAPACURONIUM plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
27.8 min |
1.5 mg/kg 1 times / day steady-state, intravenous dose: 1.5 mg/kg route of administration: Intravenous experiment type: STEADY-STATE co-administered: |
RAPACURONIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
12% |
1.5 mg/kg 1 times / day steady-state, intravenous dose: 1.5 mg/kg route of administration: Intravenous experiment type: STEADY-STATE co-administered: |
RAPACURONIUM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Other AEs: Bronchospasm, Tachycardia... Other AEs: Bronchospasm (3.4%) Sources: Tachycardia (1.6%) Injection site reaction (1.1%) Hypotension (0.9%) Airway peak pressure increased (0.6%) Erythematous rash (0.5%) Hypertension (<0.1%) Fever (<0.1%) Nausea and vomiting (<0.1%) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Erythematous rash | 0.5% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Airway peak pressure increased | 0.6% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Hypotension | 0.9% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Injection site reaction | 1.1% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Tachycardia | 1.6% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Bronchospasm | 3.4% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Fever | <0.1% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Hypertension | <0.1% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
Nausea and vomiting | <0.1% | 3 mg/kg single, intravenous Recommended Dose: 3 mg/kg Route: intravenous Route: single Dose: 3 mg/kg Sources: |
unhealthy, adult n = 1300 Health Status: unhealthy Condition: planned operation Age Group: adult Sex: unknown Population Size: 1300 Sources: |
PubMed
Title | Date | PubMed |
---|---|---|
Time course of action and endotracheal intubating conditions of Org 9487, a new short-acting steroidal muscle relaxant; a comparison with succinylcholine. | 1993 Sep |
|
Preliminary investigations of the clinical pharmacology of three short-acting non-depolarizing neuromuscular blocking agents, Org 9453, Org 9489 and Org 9487. | 1994 Mar |
|
A mechanism for rapacuronium-induced bronchospasm: M2 muscarinic receptor antagonism. | 2003 Apr |
|
Rapacuronium preferentially antagonizes the function of M2 versus M3 muscarinic receptors in guinea pig airway smooth muscle. | 2005 Jan |
|
In silico prediction of blood brain barrier permeability: an Artificial Neural Network model. | 2006 Jan-Feb |
|
Divergence of allosteric effects of rapacuronium on binding and function of muscarinic receptors. | 2009 Dec 28 |
|
Determining the potency of neuromuscular blockers: are traditional methods flawed? | 2010 Jun |
Patents
Sample Use Guides
The adult (1.5 mg/kg), pediatric (2.0 mg/kg), and Cesarean section (2.5 mg/kg)
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20038295
Effects of 10 uM rapacuronium on the dissociation rate of high-affinity [3H]ACh binding were measured after 60 min preincubation of membranes with 40 nM [3H]ACh. Dissociation was evoked by the addition of unlabeled ACh at a final concentration of 40 uM, either alone or mixed with 10 uM rapacuronium. The slower phase of [3H]ACh dissociation displayed a rate (koff) in the range of 0.112 (M5) to 0.507 (M2) min-1.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:58:40 GMT 2023
by
admin
on
Fri Dec 15 15:58:40 GMT 2023
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Record UNII |
65Q4QDG4KC
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Record Status |
Validated (UNII)
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Record Version |
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C29696
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DTXSID7048823
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7635
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m9501
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CHEMBL1201352
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SUB10260MIG
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156137-99-4
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Rapacuronium bromide
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65Q4QDG4KC
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C66509
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ACTIVE MOIETY |
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