CISAPRID MONOHYDRAT

Cisapride monohydrate enhances GI motility by stimulating serotonin receptors. Side effects include diarrhea, cramping, and risk of arrhythmias.

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Product Description


Mechanism of Action

Cisapride monohydrate is a prokinetic agent that enhances acetylcholine release in the enteric nervous system via 5-HT₄ receptor agonism and inhibits 5-HT₃-mediated reflex inhibition. This accelerates gastric emptying and increases lower-esophageal sphincter tone. It does not significantly block dopamine receptors.

Benefits and Advantages

Used in GI-motility research, serotonergic signalling studies, enteric-neuron modelling, gastroparesis research and prokinetic drug-development assays.

Side Effects and Risks

Risks include QT prolongation, arrhythmias (torsades de pointes), diarrhea, abdominal cramping and drug–drug interactions via CYP3A4. Handle with cardiac-safety precautions.

Datasheet


Molecular Formula

C23H29ClFN4O5

Molecular Weight

498.95 g/mol

CAS Number

76479-27-3

Storage Condition

Store in a cool, dry place; protect from light

Solubility

Soluble in water

Purity

Purity information is available upon request (COA).

IUPAC/Chemical Name

4-amino-5-chloro-N-[1-[3-(4-fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide monohydrate

InChl Key

Unavailable

InChl Code

Unavailable

References

PubChem; ChemBL; FDA;

3D Conformer.

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