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70181-03-2

70181-03-2 structure
70181-03-2 structure
  • Name: Dazopride
  • Chemical Name: 4-amino-5-chloro-N-(1,2-diethylpyrazolidin-4-yl)-2-methoxybenzamide
  • CAS Number: 70181-03-2
  • Molecular Formula: C15H23ClN4O2
  • Molecular Weight: 326.82200
  • Catalog: Research Areas Others
  • Create Date: 2018-07-23 16:03:09
  • Modify Date: 2024-01-08 20:13:40
  • Dazopride is an antiemetic agent.

Name 4-amino-5-chloro-N-(1,2-diethylpyrazolidin-4-yl)-2-methoxybenzamide
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.
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

[1]. Alphin RS, et al. Antagonism of cisplatin-induced emesis by metoclopramide and dazopride through enhancement of gastric motility. Dig Dis Sci. 1986 May;31(5):524-9.

[2]. Costall B, et al. The action of dazopride to enhance gastric emptying and block emesis. Neuropharmacology. 1987 Jul;26(7A):669-77.

Density 1.27g/cm3
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℃

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70181-03-2 structure

70181-03-2

Literature: A. H. Robins Company, Inc. Patent: US4207327 A1, 1980 ;
Precursor  2

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