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The chemical structure of mosapride citrate is similar to cisapride , both of which are benzamide derivatives. The mechanism of gastric motility of the two drugs is also similar, both promote gastric emptying by stimulating the 5-HT4 receptors of the muscular plexus of the intestine, resulting in increased acetylcholine release of nerve endings. Unlike cisapride , mosapride citrate selectively acts on the upper gastrointestinal tract and has no effect on colonic motility, reducing side effects such as abdominal pain, increased frequency of bowel movements, diarrhea and soft stools due to colonic hypermotility, and because it has no affinity with dopamine D2 receptors, it can avoid side effects such as extrapyramidal reactions and increased prolactin secretion caused by antagonism of dopamine D2 receptors.
Mosapride citrate is used for the relief of chronic gastritis, functional dyspepsia, reflux esophagitis and a range of gastrointestinal symptoms associated with surgery.
| Item | Specifications | Results |
| Appearance | White to off white crystalline powder | Conform |
| Heavy Metal | ≤10ppm | Conform |
| Water | 5.0 – 6.0% | 5.6% |
| Residue on ignition | ≤0.1% | 0.02% |
| Assay | 98.0% - 101.5% | 99.5% |
| Product parameters | |
| Cas number: | 112885-42-4 |
| Appearance: | White to off white crystalline powder |
| Purity: | 98.0% - 101.5% |
| Package details: | 1kg/foil bag,25kg/drum |
| Brand: | Fortunachem |
Mosapride citrate is the citrate salt of mosapride, a selective 5-HT₄ (serotonin) receptor agonist used clinically as a gastroprokinetic agent to enhance gastric motility. Chemically, it is a benzamide derivative.
Pharmaceutical Grade: Formulated into tablets for treating functional dyspepsia, gastroesophageal reflux disease (GERD), and gastroparesis.
Chemical/Research Grade: A high-purity (typically ≥98%), solid powder with a defined chemical structure (CAS: 112885-42-4), sold for non-therapeutic laboratory use.
As a research chemical, it serves as a selective pharmacological tool:
Biochemical & Pharmacological Research:
Selective 5-HT₄ Receptor Agonist: Used in in vitro assays (e.g., cell lines expressing 5-HT₄ receptors) and in vivo animal models to study the specific role of 5-HT₄ receptor signaling in gastrointestinal motility, visceral sensitivity, and neurotransmitter release.
Mechanism Studies: A tool to investigate downstream pathways of 5-HT₄ activation and compare efficacy/selectivity against other prokinetic agents (e.g., metoclopramide).
Analytical Reference Standard:
Primary Standard: Used in HPLC, LC-MS/MS, and other analytical methods for quantitative analysis, quality control, and method validation during pharmaceutical manufacturing of mosapride products.
Bioanalytical Applications: Essential for developing assays to measure mosapride concentration in biological samples (plasma, tissue) for pharmacokinetic and metabolism studies.
Metabolic and Toxicology Studies:
Used to identify and characterize its metabolites (primarily via CYP3A4 metabolism) and to assess preclinical safety profiles in controlled research settings.
Not for Human Use: Strictly for laboratory research.
Handling & Storage: Store in a cool, dry place. Handle using standard laboratory safety practices; avoid inhalation or direct contact.
Solubility: Soluble in DMSO and methanol, slightly soluble in water, which informs its preparation for in vitro studies.
| Aspect | Description |
|---|---|
| Identity | Citrate salt of a selective 5-HT₄ receptor agonist (benzamide class). |
| Chemical Grade | High-purity reference material for non-therapeutic research. |
| Primary Research Uses | 1. Pharmacological Tool: For selective 5-HT₄ receptor studies in GI physiology. 2. Analytical Standard: For quantification and method validation. 3. Metabolism Studies: To investigate its metabolic fate. |
In essence, chemical-grade mosapride citrate is a selective receptor agonist used as a precise tool for gastrointestinal pharmacology research, analytical chemistry, and drug metabolism studies.




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