Praziquantel

CHEMBL976 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
312.4 g/mol
LogP
2.7
Phase
4

An antiparasitic medication used to treat a variety of parasitic worm infections, including schistosomiasis and tapeworm infections, by causing paralysis and damage to the worms so the body can eliminate them. It is typically taken as a single dose or short course and is considered highly effective against susceptible parasites.

Molecular Weight

312.4000 g/mol

LogP

2.70

TPSA

40.60 Ų

Lipinski RO5

Pass

Therapeutic Areas

Mechanism of Action

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

2D Structure

SVG PNG

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SMILES

O=C(C1CCCCC1)N1CC(=O)N2CCc3ccccc3C2C1

InChI

InChI=1S/C19H24N2O2/c22-18-13-20(19(23)15-7-2-1-3-8-15)12-17-16-9-5-4-6-14(16)10-11-21(17)18/h4-6,9,15,17H,1-3,7-8,10-13H2

Molecular Formula

C19H24N2O2

HBD / HBA

- / 2

Rotatable Bonds

1

Heavy Atoms

23

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

An antiparasitic medication used to treat a variety of parasitic worm infections, including schistosomiasis and tapeworm infections, by causing paralysis and damage to the worms so the body can eliminate them. It is typically taken as a single dose or short course and is considered highly effective against susceptible parasites.

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

Yes, Praziquantel 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). CHEMBL976. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4891. Chemical information database.

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

Medical Disclaimer

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.