Ondansetron Hydrochloride
A hydrochloride salt form of ondansetron with the same therapeutic properties. A serotonin receptor antagonist preventing chemotherapy-induced and post-operative nausea and vomiting.
Khối lượng phân tử
329,8000 g/mol
TPSA
39,80 Ų
Lĩnh vực điều trị
Cơ chế tác dụng
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.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O.Cl.O.O
InChI
InChI=1S/C18H19N3O.ClH.2H2O/c1-12-19-9-10-21(12)11-13-7-8-16-17(18(13)22)14-5-3-4-6-15(14)20(16)2;;;/h3-6,9-10,13H,7-8,11H2,1-2H3;1H;2*1H2
Molecular Formula
C18H20ClN3O
HBD / HBA
1 / 2
Liên kết có thể quay
2
Nguyên tử nặng
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.
Câu hỏi thường gặp
A hydrochloride salt form of ondansetron with the same therapeutic properties. A serotonin receptor antagonist preventing chemotherapy-induced and post-operative nausea and vomiting.
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Yes, Ondansetron Hydrochloride 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). CHEMBL3186492. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 68647. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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