Radiosynthesis of dimethyl-2-[18F]-(fluoromethyl)-6-methyl-4-(2- nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate for L-type calcium channel imaging

7Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

Dimethyl 2-(fluoromethyl)-6-methyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3, 5-dicarboxylate 4a, a fluorinated nifedipine analog, has been shown to elicit significant calcium channel blocker activity using a guinea pig ileal longitudinal smooth muscle model. In order to perform biological studies for detection of L-type calcium channel distribution, we decided to prepare the [18F]-labeled compound. The latter compound was prepared in no-carrier-added (n.c.a.) form from dimethyl 2-(bromomethyl)-6-methyl-4-(2- nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate 2 in one step at 80°C in Kryptofix[222]/K[18F]F and acetonitrile as a solvent in 15 min. Column chromatography afforded the radiochemically pure compound in 20 min. Radiochemical purity of the 18F-nifedipine was determined by RTLC and HPLC (> 98%) and specific activity of 21-48 GBq/μmol (EOB). © by Oldenbourg Wissenschaftsverlag.

Cite

CITATION STYLE

APA

Sadeghpour, H., Jalilian, A. R., Shafiee, A., Akhlaghi, M., Miri, R., & Mirzaei, M. (2008). Radiosynthesis of dimethyl-2-[18F]-(fluoromethyl)-6-methyl-4-(2- nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate for L-type calcium channel imaging. Radiochimica Acta, 96(12), 849–853. https://doi.org/10.1524/ract.2008.1567

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free