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70181-03-2

70181-03-2 Structure

70181-03-2 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[pka]

13.31±0.20(Predicted)
Hazard InformationBack 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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