Levobupivacaine

CHEMBL1201193 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
288.4 g/mol
LogP
3.4
Phase
4

The S-enantiomer of bupivacaine, a long-acting local anesthetic used for regional anesthesia and pain management. It is considered to have a better safety profile than racemic bupivacaine, particularly regarding cardiac toxicity.

분자량

288.4000 g/mol

LogP

3.40

TPSA

32.30 Ų

리핀스키 5의 법칙

통과

치료 영역

작용 기전

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)

기전

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.

2D 구조

SVG PNG

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SMILES

CCCCN1CCCC[C@H]1C(=O)Nc1c(C)cccc1C

InChI

InChI=1S/C18H28N2O/c1-4-5-12-20-13-7-6-11-16(20)18(21)19-17-14(2)9-8-10-15(17)3/h8-10,16H,4-7,11-13H2,1-3H3,(H,19,21)/t16-/m0/s1

Molecular Formula

C18H28N2O

HBD / HBA

1 / 2

회전 가능 결합

5

무거운 원자

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.

자주 묻는 질문

The S-enantiomer of bupivacaine, a long-acting local anesthetic used for regional anesthesia and pain management. It is considered to have a better safety profile than racemic bupivacaine, particularly regarding cardiac toxicity.

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, Levobupivacaine 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). CHEMBL1201193. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 92253. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

의학적 면책조항

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.