Ropivacaine Hydrochloride

CHEMBL1889140 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
310.9 g/mol
LogP
Phase
4

The hydrochloride salt formulation of ropivacaine used for epidural anesthesia during labor and delivery, and for post-surgical pain control through continuous nerve block infusions. Its long duration of action provides several hours of effective pain relief.

Berat Molekul

310,9000 g/mol

TPSA

32,30 Ų

Area Terapeutik

Mekanisme Kerja

Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.

Struktur 2D

SVG PNG

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SMILES

CCCN1CCCC[C@H]1C(=O)Nc1c(C)cccc1C.Cl

InChI

InChI=1S/C17H26N2O.ClH/c1-4-11-19-12-6-5-10-15(19)17(20)18-16-13(2)8-7-9-14(16)3;/h7-9,15H,4-6,10-12H2,1-3H3,(H,18,20);1H/t15-;/m0./s1

Molecular Formula

C17H27ClN2O

HBD / HBA

2 / 2

Ikatan yang Dapat Dirotasi

4

Atom Berat

21

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.

Pertanyaan yang Sering Diajukan

The hydrochloride salt formulation of ropivacaine used for epidural anesthesia during labor and delivery, and for post-surgical pain control through continuous nerve block infusions. Its long duration of action provides several hours of effective pain relief.

Blocks voltage-gated sodium channels in nerve cell membranes, preventing the generation and conduction of nerve impulses. This produces reversible loss of sensation in the area of application.

Yes, Ropivacaine Hydrochloride 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). CHEMBL1889140. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 175804. Chemical information database.

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

Penyangkalan Medis

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.