Tubocurarine Chloride
Tubocurarine chloride is the chloride salt of tubocurarine, the prototype non-depolarizing neuromuscular blocking agent that competitively blocks nicotinic receptors at the motor end plate to produce reversible skeletal muscle paralysis. It was used as an anesthetic adjunct for surgical muscle relaxation and to facilitate endotracheal intubation. It has been superseded by agents with shorter duration, more predictable reversal, and fewer adverse effects.
Молекулярная масса
681,6000 g/mol
TPSA
80,60 Ų
Механизм действия
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
2D Структура
Cite this structure
Embed this structure
SMILES
COc1cc2c3cc1Oc1cc(ccc1O)C[C@@H]1c4c(cc(OC)c(O)c4Oc4ccc(cc4)C[C@@H]3N(C)CC2)CC[N+]1(C)C.Cl.O.O.O.O.O.[Cl-]
InChI
InChI=1S/C37H40N2O6.2ClH.5H2O/c1-38-14-12-24-19-32(42-4)33-21-27(24)28(38)16-22-6-9-26(10-7-22)44-37-35-25(20-34(43-5)36(37)41)13-15-39(2,3)29(35)17-23-8-11-30(40)31(18-23)45-33;;;;;;;/h6-11,18-21,28-29H,12-17H2,1-5H3,(H-,40,41);2*1H;5*1H2/t28-,29+;;;;;;;/m0......./s1
Molecular Formula
C37H42Cl2N2O6
HBD / HBA
3 / 8
Вращаемые Связи
2
Тяжёлые Атомы
47
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Часто задаваемые вопросы
Tubocurarine chloride is the chloride salt of tubocurarine, the prototype non-depolarizing neuromuscular blocking agent that competitively blocks nicotinic receptors at the motor end plate to produce reversible skeletal muscle paralysis. It was used as an anesthetic adjunct for surgical muscle relaxation and to facilitate endotracheal intubation. It has been superseded by agents with shorter duration, more predictable reversal, and fewer adverse effects.
Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.
Yes, Tubocurarine Chloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3989821. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 16051918. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
Медицинский отказ от ответственности
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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