Alosetron

CHEMBL1110 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
294.4 g/mol
LogP
1.6
Phase
4

A selective serotonin 5-HT3 receptor antagonist that reduces the hypersensitivity and abnormal gut contractions characteristic of severe diarrhea-predominant irritable bowel syndrome (IBS-D) in women. By blocking these receptors in the gut, it slows intestinal transit, reduces urgency, and decreases pain.

Peso molecular

294,3500 g/mol

LogP

1,60

TPSA

53,90 Ų

Regla de cinco de Lipinski

Cumple

Mecanismo de acción

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Estructura 2D

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SMILES

Cc1[nH]cnc1CN1CCc2c(c3ccccc3n2C)C1=O

InChI

InChI=1S/C17H18N4O/c1-11-13(19-10-18-11)9-21-8-7-15-16(17(21)22)12-5-3-4-6-14(12)20(15)2/h3-6,10H,7-9H2,1-2H3,(H,18,19)

Molecular Formula

C17H18N4O

HBD / HBA

1 / 2

Enlaces Rotables

2

Átomos Pesados

22

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.

Preguntas frecuentes

A selective serotonin 5-HT3 receptor antagonist that reduces the hypersensitivity and abnormal gut contractions characteristic of severe diarrhea-predominant irritable bowel syndrome (IBS-D) in women. By blocking these receptors in the gut, it slows intestinal transit, reduces urgency, and decreases pain.

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Yes, Alosetron 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). CHEMBL1110. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2099. Chemical information database.

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

Aviso médico

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.