Desmethoxyfallypride

Desmethoxyfallypride (¹⁸F)
Clinical data
Other names	DMFP (18F)
Pregnancy; category	N/A;
ATC code	none;
Legal status
Legal status	Research compound;
Identifiers
	IUPAC name 5-(3-18F-fluoropropyl)-2-methoxy-N-[(2S)-1-prop-2-enylpyrrolidin-2-yl]methyl]benzamide;
PubChem CID	9543408;
ChemSpider	8580101;
Chemical and physical data
Formula	C19H27FN2O2
Molar mass	334.435 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES COC1=C(C=C(C=C1)CCCF)C(=O)NC[C@@H]2CCCN2CC=C;
	InChI InChI=1S/C19H27FN2O2/c1-3-11-22-12-5-7-16(22)14-21-19(23)17-13-15(6-4-10-20)8-9-18(17)24-2/h3,8-9,13,16H,1,4-7,10-12,14H2,2H3,(H,21,23)/t16-/m0/s1; Key:VPBJNBUDASILSQ-INIZCTEOSA-N;

Desmethoxyfallypride is a moderate affinity dopamine D2 receptor/D3 receptor antagonist used in medical research, usually in the form of the radiopharmaceuticals desmethoxyfallypride or DMFP(¹⁸F)[1][2] and has been used in human studies[3][4] as a positron emission tomography (PET) radiotracer.

References

Mukherjee J, Yang ZY, Brown T, Roemer J, Cooper M (1996). "18F-desmethoxyfallypride: a fluorine-18 labeled radiotracer with properties similar to carbon-11 raclopride for PET imaging studies of dopamine D2 receptors". Life Sciences. 59 (8): 669–78. doi:10.1016/0024-3205(96)00348-7. PMID 8761017.
Leung, K. (2004). "(S)-N-((1-Allyl-2-pyrrolidinyl)methyl)-5-(3-¹⁸Ffluoropropyl)-2-methoxybenzamide". PMID 20641474. Cite journal requires |journal= (help)
Gründer G, Siessmeier T, Piel M, Vernaleken I, Buchholz HG, Zhou Y, et al. (January 2003). "Quantification of D2-like dopamine receptors in the human brain with 18F-desmethoxyfallypride". Journal of Nuclear Medicine. 44 (1): 109–16. PMID 12515884.
Siessmeier T, Zhou Y, Buchholz HG, Landvogt C, Vernaleken I, Piel M, et al. (June 2005). "Parametric mapping of binding in human brain of D2 receptor ligands of different affinities". Journal of Nuclear Medicine. 46 (6): 964–72. PMID 15937307.

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