Dolasetron Mesylate

CHEMBL2368924 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
438.5 g/mol
LogP
Phase
4

The mesylate salt form of dolasetron, used in oral and injectable preparations for antiemetic therapy. It blocks 5-HT3 receptors to prevent chemotherapy-induced and postoperative nausea and vomiting. This salt form improves solubility for pharmaceutical formulation.

Molecular Weight

438.5000 g/mol

TPSA

126.00 Ų

Mechanism of Action

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

2D Structure

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SMILES

CS(=O)(=O)O.O.O=C(O[C@@H]1C[C@@H]2C[C@H]3C[C@H](C1)N2CC3=O)c1c[nH]c2ccccc12

InChI

InChI=1S/C19H20N2O3.CH4O3S.H2O/c22-18-10-21-12-5-11(18)6-13(21)8-14(7-12)24-19(23)16-9-20-17-4-2-1-3-15(16)17;1-5(2,3)4;/h1-4,9,11-14,20H,5-8,10H2;1H3,(H,2,3,4);1H2/t11-,12-,13+,14+;;

Molecular Formula

C20H26N2O7S

HBD / HBA

3 / 8

Rotatable Bonds

3

Heavy Atoms

30

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

The mesylate salt form of dolasetron, used in oral and injectable preparations for antiemetic therapy. It blocks 5-HT3 receptors to prevent chemotherapy-induced and postoperative nausea and vomiting. This salt form improves solubility for pharmaceutical formulation.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Dolasetron Mesylate 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). CHEMBL2368924. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6918119. Chemical information database.

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

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.