Chloroprocaine

CHEMBL1179047 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
270.8 g/mol
LogP
2.9
Phase
4

A short-acting local anesthetic of the ester class that blocks sodium channels to reversibly inhibit nerve conduction, used primarily for epidural and spinal anesthesia in obstetric procedures. Its rapid hydrolysis by plasma cholinesterases results in a short duration of action and low systemic toxicity. It is particularly valued in obstetrics due to its rapid onset and safety profile for the neonate.

Molekularmasse

270,7500 g/mol

LogP

2,90

TPSA

55,60 Ų

Lipinski-Regel der Fünf

Bestanden

Therapeutische Bereiche

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

Cite this structure


                        

Embed this structure


                        

SMILES

CCN(CC)CCOC(=O)c1ccc(N)cc1Cl

InChI

InChI=1S/C13H19ClN2O2/c1-3-16(4-2)7-8-18-13(17)11-6-5-10(15)9-12(11)14/h5-6,9H,3-4,7-8,15H2,1-2H3

Molecular Formula

C13H19ClN2O2

HBD / HBA

1 / 4

Rotierbare Bindungen

7

Schwere Atome

18

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

A short-acting local anesthetic of the ester class that blocks sodium channels to reversibly inhibit nerve conduction, used primarily for epidural and spinal anesthesia in obstetric procedures. Its rapid hydrolysis by plasma cholinesterases results in a short duration of action and low systemic toxicity. It is particularly valued in obstetrics due to its rapid onset and safety profile for the neonate.

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, Chloroprocaine 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). CHEMBL1179047. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 8612. Chemical information database.

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

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.