Identification | Back Directory | [Name]
Dazopride | [CAS]
70181-03-2 | [Synonyms]
AHR-5531 Dazopride 4-Amino-5-chloro-N-(1,2-diethyl-4-pyrazolidinyl)-2-methoxybenzamide 4-amino-5-chloro-N-(1,2-diethylpyrazolidin-4-yl)-2-methoxybenzamide Benzamide, 4-amino-5-chloro-N-(1,2-diethyl-4-pyrazolidinyl)-2-methoxy- | [Molecular Formula]
C15H23ClN4O2 | [MDL Number]
MFCD00867811 | [MOL File]
70181-03-2.mol | [Molecular Weight]
326.82 |
Hazard Information | Back Directory | [Uses]
Stimulant (peristaltic). | [Definition]
ChEBI: Dazopride is a member of benzamides. | [in vivo]
Dazopride (0.3 mg/kg) produces significant enhancement of gastric evacuation and is approximately six times more potent than metoclopramide in gastric evacuation assay. Dazopride (0.3-10.0 mg/kg, i.v.) produces a dose-related increase in antral motility primarily by increasing the amplitude of antral contractions in three conscious dogs. Dazopride significantly reduces the emetic frequency from that of the control group[1]. Dazopride (5 mg/kg, i.p.) antagonises the tetralin-induced emesis in all animals, but fails to antagonise the response at 0.25-2.5 mg/kg. Dazopride fails to modify cisplatin-induced emesis at 0.1 mg/kg (i.v,) although a larger dose of 1.0 mg/kg abolishes or attenuates the response and 5.0 mg/kg of dazopride antagonises the development ofemesis in all animals[2]. | [storage]
Store at -20°C |
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