Tegaserod

CHEMBL76370 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
301.4 g/mol
LogP
2.6
Phase
4

Tegaserod is a selective partial agonist of serotonin 5-HT4 receptors in the gastrointestinal tract that stimulates peristaltic reflexes, intestinal secretion, and reduces visceral sensitivity, originally used for irritable bowel syndrome with constipation and chronic idiopathic constipation. It was withdrawn from the US market due to cardiovascular risks but has been reapproved at lower doses for IBS-C in women under 65 without cardiovascular disease. Research has also explored its potential neuroprotective effects in Alzheimer's disease through serotonergic pathways.

น้ำหนักโมเลกุล

301.3900 g/mol

LogP

2.60

TPSA

87.80 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

Pharmacokinetics (PK)

Pharmacodynamics (PD)

โครงสร้าง 2 มิติ

SVG PNG

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SMILES

CCCCCNC(=N)N/N=C/c1c[nH]c2ccc(OC)cc12

InChI

InChI=1S/C16H23N5O/c1-3-4-5-8-18-16(17)21-20-11-12-10-19-15-7-6-13(22-2)9-14(12)15/h6-7,9-11,19H,3-5,8H2,1-2H3,(H3,17,18,21)/b20-11+

Molecular Formula

C16H23N5O

HBD / HBA

3 / 3

พันธะที่หมุนได้

8

อะตอมหนัก

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.

คำถามที่พบบ่อย

Tegaserod is a selective partial agonist of serotonin 5-HT4 receptors in the gastrointestinal tract that stimulates peristaltic reflexes, intestinal secretion, and reduces visceral sensitivity, originally used for irritable bowel syndrome with constipation and chronic idiopathic constipation. It was withdrawn from the US market due to cardiovascular risks but has been reapproved at lower doses for IBS-C in women under 65 without cardiovascular disease. Research has also explored its potential neuroprotective effects in Alzheimer's disease through serotonergic pathways.

Yes, Tegaserod 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). CHEMBL76370. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 135409453. Chemical information database.

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

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.

Data sources: ChEMBL, PubChem, DailyMed.