Azapride

Azapride
Clinical data
Other names	Azidoclebopride
ATC code	None;
Identifiers
	IUPAC name 4-Azido-5-chloro-2-methoxy-N-[1-(phenylmethyl)piperidin-4-yl]benzamide;
CAS Number	92990-90-4 ;
PubChem CID	3036441;
ChemSpider	2300456 ;
CompTox Dashboard (EPA)	DTXSID00239217 ;
Chemical and physical data
Formula	C20H22ClN5O2
Molar mass	399.88 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES Clc1cc(c(OC)cc1/N=[N+]=[N-])C(=O)NC3CCN(Cc2ccccc2)CC3;
	InChI 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) ; Key:CKKHIIXHAWWTNP-UHFFFAOYSA-N ;
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Azapride is the azide derivative of the dopamine antagonist clebopride synthesized in order to label dopamine receptors.[1][2] It is an irreversible dopamine antagonist.[2]

References

Niznik, H. B; Guan, J. H; Neumeyer, J. L; Seeman, P (1985). "A photoaffinity ligand for dopamine D2 receptors: Azidoclebopride". Molecular Pharmacology. 27 (2): 193–9. PMID 3969068.
Wouters, W; Van Dun, J; Laduron, P. M (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.

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