Pipecuronium

CHEMBL1201206 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
602.9 g/mol
LogP
4.5
Phase
4

Pipecuronium is a long-acting non-depolarizing neuromuscular blocking agent of the aminosteroid class that competitively antagonizes acetylcholine at nicotinic receptors at the neuromuscular junction, producing skeletal muscle relaxation. It is used as an adjunct to general anesthesia during surgical procedures requiring prolonged muscle relaxation, particularly in patients with cardiovascular disease due to its minimal cardiovascular effects.

Khối lượng phân tử

602,9000 g/mol

LogP

4,50

TPSA

59,10 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

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)

Cơ chế

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

Cấu trúc 2D

SVG PNG

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SMILES

CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@@]4(C)[C@H]3C[C@H](N3CC[N+](C)(C)CC3)[C@@H]4OC(C)=O)[C@@]2(C)C[C@@H]1N1CC[N+](C)(C)CC1

InChI

InChI=1S/C35H62N4O4/c1-24(40)42-32-21-26-9-10-27-28(35(26,4)23-31(32)37-15-19-39(7,8)20-16-37)11-12-34(3)29(27)22-30(33(34)43-25(2)41)36-13-17-38(5,6)18-14-36/h26-33H,9-23H2,1-8H3/q+2/t26-,27+,28-,29-,30-,31-,32-,33-,34-,35-/m0/s1

Molecular Formula

C35H62N4O4+2

HBD / HBA

- / 6

Liên kết có thể quay

6

Nguyên tử nặng

43

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.

Câu hỏi thường gặp

Pipecuronium is a long-acting non-depolarizing neuromuscular blocking agent of the aminosteroid class that competitively antagonizes acetylcholine at nicotinic receptors at the neuromuscular junction, producing skeletal muscle relaxation. It is used as an adjunct to general anesthesia during surgical procedures requiring prolonged muscle relaxation, particularly in patients with cardiovascular disease due to its minimal cardiovascular 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, Pipecuronium 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). CHEMBL1201206. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 50192. Chemical information database.

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

Tuyên bố miễn trách y tế

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.