Title: Synthesis and biological evaluation of carbon-11-labeled acyclic derivatives of and furo[2,3-d]pyrimidine bicyclic nucleoside analogues (BCNAs) for structure-brain uptake relationship study of BCNA tracers
Authors: Chitneni, Satish Kumar ×
Balzarini, Jan
Celen, Sofie
Dyubankova, Natalia
Verbruggen, Alfons
Bormans, Guy #
Issue Date: Mar-2008
Publisher: Wiley
Series Title: Journal of Labelled Compounds & Radiopharmaceuticals vol:51 issue:3-4 pages:159-166
Abstract: We reported earlier on radiolabeled alkoxyphenyl bicyclic nucleoside analogues (BCNAs) as potential positron emission tomography (PET) reporter probes for imaging of varicella zoster virus thymidine kinase (VZV-tk) gene in vivo. Despite their favorable physicochemical properties, these tracers are not taken up in the brain in mice. In order to probe the role of the deoxyribose sugar moiety in blood-brain barrier (BBB) penetration of these molecules, we have synthesized and evaluated a carbon-11-labeled acyclic bicyclic nucleoside derivative ([C-11]-10) where the 2'-deoxyribose sugar is replaced with a (2-hydroxyethoxy)methyl group and [C-11]-12, which has no sugar moiety but a [C-11]methyl group on the N-3 position of the pyrimidine ring. Methylation was achieved on the phenol [C-11]-10) or the N-3 position ([C-11]-12) using [C-11]methyl triflate (radiosynthesis). The (non-radioactive) acyclic O-methyl derivative 10 has rather poor affinity for the enzyme VZV-TK in vitro (IC50: 430 mu M), compared with the moderate affinity of the BCNA-base N-methyl derivative 12 (IC50: 79 mu M). In normal mice, none of the two tracers ([C-11]-10 or [C-11]-12) showed significant uptake in the brain, suggesting that compounds containing a furo[2,3-d]pyrimidine system do not cross the BBB.
ISSN: 0362-4803
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Virology and Chemotherapy (Rega Institute)
Radiopharmaceutical Research
Medicinal Chemistry (Rega Institute)
× corresponding author
# (joint) last author

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