Granisetron Hydrochloride
A hydrochloride salt form of granisetron, a 5-HT3 antagonist antiemetic used to prevent and treat nausea and vomiting associated with chemotherapy and postoperative settings. The hydrochloride salt form is used in both oral tablets and injectable preparations. It provides effective antiemetic coverage, particularly for acute chemotherapy-induced nausea occurring within the first 24 hours of treatment.
น้ำหนักโมเลกุล
348.9000 g/mol
TPSA
50.20 Ų
ด้านการรักษา
กลไกการออกฤทธิ์
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.
โครงสร้าง 2 มิติ
Cite this structure
Embed this structure
SMILES
CN1C2CCCC1CC(NC(=O)c1nn(C)c3ccccc13)C2.Cl
InChI
InChI=1S/C18H24N4O.ClH/c1-21-13-6-5-7-14(21)11-12(10-13)19-18(23)17-15-8-3-4-9-16(15)22(2)20-17;/h3-4,8-9,12-14H,5-7,10-11H2,1-2H3,(H,19,23);1H
Molecular Formula
C18H25ClN4O
HBD / HBA
2 / 3
พันธะที่หมุนได้
2
อะตอมหนัก
24
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.
คำถามที่พบบ่อย
A hydrochloride salt form of granisetron, a 5-HT3 antagonist antiemetic used to prevent and treat nausea and vomiting associated with chemotherapy and postoperative settings. The hydrochloride salt form is used in both oral tablets and injectable preparations. It provides effective antiemetic coverage, particularly for acute chemotherapy-induced nausea occurring within the first 24 hours of treatment.
Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.
Yes, Granisetron 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). CHEMBL1237080. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 65264. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
ข้อจำกัดความรับผิดชอบทางการแพทย์
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.
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