Cisapride Monohydrate
The monohydrate form of cisapride was the standard clinical formulation of this gastroprokinetic agent. It shares the same efficacy and the same serious cardiac arrhythmia risk as the parent compound. Its withdrawal from most markets due to fatal QT prolongation represents a landmark in drug safety.
分子量
484.0000 g/mol
TPSA
87.10 Ų
治療領域
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D構造
Cite this structure
Embed this structure
SMILES
COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCOc2ccc(F)cc2)CC1OC.O
InChI
InChI=1S/C23H29ClFN3O4.H2O/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);1H2
Molecular Formula
C23H31ClFN3O5
HBD / HBA
3 / 8
回転可能結合数
9
重原子数
33
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.
よくある質問
The monohydrate form of cisapride was the standard clinical formulation of this gastroprokinetic agent. It shares the same efficacy and the same serious cardiac arrhythmia risk as the parent compound. Its withdrawal from most markets due to fatal QT prolongation represents a landmark in drug safety.
Yes, Cisapride Monohydrate 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). CHEMBL1200788. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6917697. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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