Dolasetron Mesylate
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.
Peso Molecular
438,5000 g/mol
TPSA
126,00 Ų
Mecanismo de Ação
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Estrutura 2D
Cite this structure
Embed this structure
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
Ligações Rotacionáveis
3
Átomos Pesados
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.
Perguntas frequentes
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
- 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.
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