Proparacaine
Proparacaine is a topical ophthalmic local anesthetic of the ester class that blocks voltage-gated sodium channels in corneal and conjunctival sensory nerve endings, producing rapid-onset surface analgesia of the eye. It is used exclusively as a topical ophthalmic anesthetic for procedures such as tonometry, foreign body removal, and minor ocular surgery.
Molecular Weight
294.3900 g/mol
LogP
2.70
TPSA
64.80 Ų
Lipinski RO5
Pass
Therapeutic Areas
Mechanism of Action
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)
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 Structure
Cite this structure
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SMILES
CCCOc1ccc(C(=O)OCCN(CC)CC)cc1N
InChI
InChI=1S/C16H26N2O3/c1-4-10-20-15-8-7-13(12-14(15)17)16(19)21-11-9-18(5-2)6-3/h7-8,12H,4-6,9-11,17H2,1-3H3
Molecular Formula
C16H26N2O3
HBD / HBA
1 / 5
Rotatable Bonds
10
Heavy Atoms
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.
Frequently Asked Questions
Proparacaine is a topical ophthalmic local anesthetic of the ester class that blocks voltage-gated sodium channels in corneal and conjunctival sensory nerve endings, producing rapid-onset surface analgesia of the eye. It is used exclusively as a topical ophthalmic anesthetic for procedures such as tonometry, foreign body removal, and minor ocular surgery.
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, Proparacaine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1196. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 4935. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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