Pramoxine

CHEMBL1198 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
293.4 g/mol
LogP
3.1
Phase
4

Pramoxine is a surface local anesthetic of the morpholine class that blocks voltage-gated sodium channels in sensory nerve terminals, preventing the initiation and propagation of nociceptive impulses to reduce pain and pruritus. It is used topically for the temporary relief of pain, itching, and discomfort associated with minor skin irritations, hemorrhoids, and anogenital conditions.

Molekularmasse

293,4000 g/mol

LogP

3,10

TPSA

30,90 Ų

Lipinski-Regel der Fünf

Bestanden

Wirkmechanismus

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)

Mechanismus

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-Struktur

SVG PNG

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SMILES

CCCCOc1ccc(OCCCN2CCOCC2)cc1

InChI

InChI=1S/C17H27NO3/c1-2-3-12-20-16-5-7-17(8-6-16)21-13-4-9-18-10-14-19-15-11-18/h5-8H,2-4,9-15H2,1H3

Molecular Formula

C17H27NO3

HBD / HBA

- / 4

Rotierbare Bindungen

9

Schwere Atome

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.

Häufig gestellte Fragen

Pramoxine is a surface local anesthetic of the morpholine class that blocks voltage-gated sodium channels in sensory nerve terminals, preventing the initiation and propagation of nociceptive impulses to reduce pain and pruritus. It is used topically for the temporary relief of pain, itching, and discomfort associated with minor skin irritations, hemorrhoids, and anogenital conditions.

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, Pramoxine 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). CHEMBL1198. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4886. Chemical information database.

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

Medizinischer Haftungsausschluss

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.