Levonordefrin

CHEMBL677 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
183.2 g/mol
LogP
-0.8
Phase
4

A sympathomimetic vasoconstrictor used in combination with local anesthetics in dental procedures to prolong anesthesia and reduce bleeding. It narrows blood vessels at the injection site to slow the absorption of the anesthetic.

Khối lượng phân tử

183,2000 g/mol

LogP

-0,80

TPSA

86,70 Ų

Lipinski RO5

Đạt

Lĩnh vực điều trị

Cơ chế tác dụng

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)

Cơ chế

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.

Cấu trúc 2D

SVG PNG

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SMILES

C[C@H](N)[C@H](O)c1ccc(O)c(O)c1

InChI

InChI=1S/C9H13NO3/c1-5(10)9(13)6-2-3-7(11)8(12)4-6/h2-5,9,11-13H,10H2,1H3/t5-,9-/m0/s1

Molecular Formula

C9H13NO3

HBD / HBA

4 / 4

Liên kết có thể quay

2

Nguyên tử nặng

13

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

A sympathomimetic vasoconstrictor used in combination with local anesthetics in dental procedures to prolong anesthesia and reduce bleeding. It narrows blood vessels at the injection site to slow the absorption of the anesthetic.

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, Levonordefrin 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). CHEMBL677. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 164739. Chemical information database.

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

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.