Cisapride

CHEMBL1729 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
465.9 g/mol
LogP
3.4
Phase
4

A gastroprokinetic agent that stimulated gastrointestinal motility by enhancing acetylcholine release in the gut wall through 5-HT4 receptor agonism, used for gastroesophageal reflux disease and gastroparesis. It was withdrawn from widespread use due to potentially fatal cardiac arrhythmias caused by QT interval prolongation at therapeutic doses, particularly in combination with drugs that inhibit its metabolism. It remains available on a restricted basis in some countries for exceptional cases.

น้ำหนักโมเลกุล

465.9000 g/mol

LogP

3.40

TPSA

86.10 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

Pharmacokinetics (PK)

Pharmacodynamics (PD)

โครงสร้าง 2 มิติ

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCOc2ccc(F)cc2)CC1OC

InChI

InChI=1S/C23H29ClFN3O4/c1-30-21-13-19(26)18(24)12-17(21)23(29)27-20-8-10-28(14-22(20)31-2)9-3-11-32-16-6-4-15(25)5-7-16/h4-7,12-13,20,22H,3,8-11,14,26H2,1-2H3,(H,27,29)

Molecular Formula

C23H29ClFN3O4

HBD / HBA

2 / 7

พันธะที่หมุนได้

9

อะตอมหนัก

32

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 gastroprokinetic agent that stimulated gastrointestinal motility by enhancing acetylcholine release in the gut wall through 5-HT4 receptor agonism, used for gastroesophageal reflux disease and gastroparesis. It was withdrawn from widespread use due to potentially fatal cardiac arrhythmias caused by QT interval prolongation at therapeutic doses, particularly in combination with drugs that inhibit its metabolism. It remains available on a restricted basis in some countries for exceptional cases.

Yes, Cisapride 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). CHEMBL1729. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6917698. 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.

Data sources: ChEMBL, PubChem, DailyMed.