Mosapride Citrate , ≥98% , 112885-42-4
CAS NO.:112885-42-4
Empirical Formula: C27H33ClFN3O10
Molecular Weight: 614.02
MDL number: MFCD00874415
EINECS: 601-211-6
Pack Size | Price | Stock | Quantity |
10MG | RMB263.20 | In Stock |
|
50MG | RMB903.20 | In Stock |
|
250MG | RMB3199.20 | In Stock |
|
1G | RMB7999.20 | In Stock |
|
others | Enquire |
PRODUCT Properties
Melting point: | 143-145° |
storage temp. | Inert atmosphere,2-8°C |
solubility | DMSO (Slightly), Ethanol (Slightly, Sonicated) |
form | Solid |
color | White to Off-White |
Stability: | Hygroscopic |
Description and Uses
Mosapride is an agonist of the serotonin (5-HT) receptor subtype 5-HT4 (Ki = 69.9 nM). It is selective for 5-HT4 over 5-HT1, 5-HT2, dopamine D2, and α1- and α2-adrenergic receptors but acts as a partial antagonist at 5-HT3 (Ki = 1,189 nM). It induces relaxation of precontracted rat esophageal thoracic muscularis mucosa preparations and enhances electrically evoked contractions in isolated guinea pig ileum (EC50s = 208.4 and 73.2 nM, respectively). Mosapride (0.5 and 1 mg/kg, i.v.) increases antral and duodenal, but not ileal or colonic, motility in conscious dogs. It also increases gastric emptying in rats when administered at doses ranging from 0.03 to 30 mg/kg.
Mosapride Citrate is a selective SR-4 activator and a SR-3 inhibitor.
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H302-H315-H319-H332-H335 |
Precautionary statements | P280-P305+P351+P338-P310 |
Toxicity | LD50 in male, female mice, rats (mg/kg): >3000, >3000, >3000, 1905 orally; >1000, 914, >1000, >1000 i.p.; all species >1000 s.c.; in male, female dogs (mg/kg): both >400 orally (Yatera) |