Name | 4-amino-5-chloro-N-(1,2-diethylpyrazolidin-4-yl)-2-methoxybenzamide |
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Synonyms |
Dazopride
Dazopride [INN] Dazopridum 4-amino-5-chloro-N-(1,2-diethyl-pyrazolidin-4-yl)-2-methoxy-benzamide Dazoprida 4-amino-5-chloro-2-methoxy-N-(1,2-diethyl-4-pyrazolidinyl)benzamide UNII-CV07VSP2G8 |
Description | Dazopride is an antiemetic agent. |
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Related Catalog | |
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]. |
References |
Density | 1.27g/cm3 |
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Molecular Formula | C15H23ClN4O2 |
Molecular Weight | 326.82200 |
Exact Mass | 326.15100 |
PSA | 70.83000 |
LogP | 2.44950 |
Index of Refraction | 1.6 |
Storage condition | 2-8℃ |
~% 70181-03-2 |
Literature: A. H. Robins Company, Inc. Patent: US4207327 A1, 1980 ; |
Precursor 2 | |
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DownStream 0 |