Tubocurarine

CHEMBL339427 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
609.7 g/mol
LogP
6.0
Phase
4

Tubocurarine is a non-depolarizing neuromuscular blocking agent derived from curare that competitively antagonizes nicotinic acetylcholine receptors at the neuromuscular junction, causing skeletal muscle paralysis. It was the first purified neuromuscular blocker used clinically to provide muscle relaxation during surgical procedures and mechanical ventilation. It has largely been replaced by newer agents with fewer cardiovascular side effects.

Peso molecular

609,7000 g/mol

LogP

6,00

TPSA

80,60 Ų

Regla de cinco de Lipinski

No cumple

Mecanismo de acción

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)

Mecanismo

Blocks neuromuscular transmission at the motor end plate by competing with acetylcholine for nicotinic receptor binding sites, producing skeletal muscle relaxation and paralysis.

Estructura 2D

SVG PNG

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SMILES

COc1cc2c3cc1Oc1cc(ccc1O)C[C@@H]1c4c(cc(OC)c(O)c4Oc4ccc(cc4)C[C@@H]3N(C)CC2)CC[N+]1(C)C

InChI

InChI=1S/C37H40N2O6/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)/p+1/t28-,29+/m0/s1

Molecular Formula

C37H41N2O6+

HBD / HBA

2 / 7

Enlaces Rotables

2

Átomos Pesados

45

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.

Preguntas frecuentes

Tubocurarine is a non-depolarizing neuromuscular blocking agent derived from curare that competitively antagonizes nicotinic acetylcholine receptors at the neuromuscular junction, causing skeletal muscle paralysis. It was the first purified neuromuscular blocker used clinically to provide muscle relaxation during surgical procedures and mechanical ventilation. It has largely been replaced by newer agents with fewer cardiovascular side effects.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 is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL339427. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6000. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso médico

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.

Data sources: ChEMBL, PubChem, DailyMed.