Mosapride

• Description:

  Mosapride is an orally active gastroenterokinetic compound. Mosapride is a 5HT4 agonist. Mosapride is a CYP inducer. Mosapride has a concentration-dependent inhibitory effect on Kv4.3, and its IC50 value is 15.2 μM. Mosapride can be used in the study of gastrointestinal diseases[1][2][3][4][5][6][7].

• Product Name Alternative:

  TAK-370; AS-4370

• UNSPSC:

  12352005

• Hazard Statement:

  H302, H315, H319, H332, H335

• Target:

  5-HT Receptor; Cytochrome P450; Potassium Channel

• Type:

  Reference compound

• Related Pathways:

  GPCR/G Protein; Membrane Transporter/Ion Channel; Metabolic Enzyme/Protease; Neuronal Signaling

• Applications:

  Neuroscience-Neuromodulation

• Field of Research:

  Neurological Disease; Cancer

• Assay Protocol:

  https://www.medchemexpress.com/mosapride.html

• Purity:

  99.87

• Solubility:

  DMSO : 66.67 mg/mL (ultrasonic; warming; heat to 60°C)

• Smiles:

  O=C (NCC1CN (CC2=CC=C (F) C=C2) CCO1) C3=CC (Cl) =C (N) C=C3OCC

• Molecular Formula:

  C21H25ClFN3O3

• Molecular Weight:

  421.89

• Precautions:

  H302, H315, H319, H332, H335

• References & Citations:

  [1]Tack J, et al. Systematic review: cardiovascular safety profile of 5-HT (4) agonists developed for gastrointestinal disorders. Aliment Pharmacol Ther. 2012 Apr;35 (7) :745-67.|[2]Curran MP, et al. Mosapride in gastrointestinal disorders. Drugs. 2008;68 (7) :981-91.|[3]Kim HS, et al. The effect of mosapride citrate on proximal and distal colonic motor function in the guinea-pig in vitro. Neurogastroenterol Motil. 2008 Feb;20 (2) :169-76.|[4]Kim YH, et al. Measurement of Human Cytochrome P450 Enzyme Induction Based on Mesalazine and Mosapride Citrate Treatments Using a Luminescent Assay. Biomol Ther (Seoul) . 2015 Sep;23 (5) :486-92.|[5]Uchida M, et al. Dual role of mosapride citrate hydrate on the gastric emptying evaluated by the breath test in conscious rats. J Pharmacol Sci. 2013;121 (4) :282-7.|[6]Fujisawa M, et al. The 5-HT4 receptor agonist mosapride attenuates NSAID-induced gastric mucosal damage. J Gastroenterol. 2010 Feb;45 (2) :179-86.|[7]Sung KW, et al. Effect of mosapride on Kv4.3 potassium channels expressed in CHO cells. Naunyn Schmiedebergs Arch Pharmacol. 2013 Oct;386 (10) :905-16.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category:

  Reference compound1

• Clinical Information:

  Launched

• Isoform:

  Apolipoprotein D

• Citation 01:

  Chin J Integr Med. 2023 Sep;29 (9) :809-817.|Drug Metab Pharmacokinet. 2020 Feb;35 (1) :102-110.|J Ethnopharmacol. 2024 Jul 15:329:118118.|Nat Prod Commun. 2025 Jul 21.|Dig Dis Sci. 2025 Nov 15.|J Appl Microbiol. 2023 Aug 1;134 (8) :lxad153.

• CAS Number:

  112885-41-3