Levobupivacaine

CHEMBL1201193 Phase 4 ได้รับการอนุมัติ 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.

น้ำหนักโมเลกุล

288.4000 g/mol

LogP

3.40

TPSA

32.30 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

กลไกการออกฤทธิ์

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)

กลไก

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.

โครงสร้าง 2 มิติ

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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

พันธะที่หมุนได้

5

อะตอมหนัก

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.

คำถามที่พบบ่อย

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.

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.