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Azapride

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Azapride
Clinical data
Other namesAzidoclebopride
ATC code
  • None
Identifiers
  • 4-Azido-5-chloro-2-methoxy-N-[1-(phenylmethyl)piperidin-4-yl]benzamide
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H22ClN5O2
Molar mass399.88 g·mol−1
3D model (JSmol)
  • Clc1cc(c(OC)cc1/N=[N+]=[N-])C(=O)NC3CCN(Cc2ccccc2)CC3
  • InChI=1S/C20H22ClN5O2/c1-28-19-12-18(24-25-22)17(21)11-16(19)20(27)23-15-7-9-26(10-8-15)13-14-5-3-2-4-6-14/h2-6,11-12,15H,7-10,13H2,1H3,(H,23,27) checkY
  • Key:CKKHIIXHAWWTNP-UHFFFAOYSA-N checkY
  (verify)

Azapride is theazide derivative of thedopamine antagonistclebopride synthesized in order to label dopamine receptors.[1][2] It is an irreversibledopamine antagonist.[2]

References

[edit]
  1. ^Niznik HB, Guan JH, Neumeyer JL, Seeman P (February 1985). "A photoaffinity ligand for dopamine D2 receptors: azidoclebopride".Molecular Pharmacology.27 (2):193–9.doi:10.1016/S0026-895X(25)12275-X.PMID 3969068.
  2. ^abWouters W, Van Dun J, Laduron PM (December 1984)."Photoaffinity labelling of dopamine receptors. Synthesis and binding characteristics of azapride".European Journal of Biochemistry.145 (2):273–8.doi:10.1111/j.1432-1033.1984.tb08548.x.PMID 6548707.
D1-like
Agonists
PAMs
Antagonists
D2-like
Agonists
Antagonists
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