Ramosetron

CHEMBL1643895 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
279.3 g/mol
LogP
2.2
Phase
4

Ramosetron is a potent and selective 5-HT3 serotonin receptor antagonist that blocks serotonin-mediated signals in the vagal afferents and central chemoreceptor trigger zone, preventing nausea and vomiting. It is approved in several Asian countries for the prevention of chemotherapy-induced nausea and vomiting and for the treatment of irritable bowel syndrome with diarrhea.

分子量

279.3400 g/mol

LogP

2.20

TPSA

50.70 Ų

Lipinski 五规则

符合

治疗领域

作用机制

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

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

二维结构

SVG PNG

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SMILES

Cn1cc(C(=O)[C@@H]2CCc3[nH]cnc3C2)c2ccccc21

InChI

InChI=1S/C17H17N3O/c1-20-9-13(12-4-2-3-5-16(12)20)17(21)11-6-7-14-15(8-11)19-10-18-14/h2-5,9-11H,6-8H2,1H3,(H,18,19)/t11-/m1/s1

Molecular Formula

C17H17N3O

HBD / HBA

1 / 2

可旋转键数

2

重原子数

21

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.

常见问题

Ramosetron is a potent and selective 5-HT3 serotonin receptor antagonist that blocks serotonin-mediated signals in the vagal afferents and central chemoreceptor trigger zone, preventing nausea and vomiting. It is approved in several Asian countries for the prevention of chemotherapy-induced nausea and vomiting and for the treatment of irritable bowel syndrome with diarrhea.

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

Yes, Ramosetron 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). CHEMBL1643895. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 108000. Chemical information database.

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

医疗免责声明

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.