Synthesis of 11C-labelled benzamide compounds as potential tracers for poly(ADP-ribose) synthetase

Abstract

Poly (ADP-ribose) synthetase catalyses the synthesis of poly (ADP-ribose) from NAD +, thereby releasing the DNA from histones to a transcriptionally and reparationally active form. In order to investigate if in vivo and in vitro studies of this enzyme are feasible to perform with PET, the poly (ADP-ribose) synthetase inhibitors benzamide, 3-aminobenzamide, 3-methoxybenzamide and nicotinamide were labelled with carbon-11 in the amide group. Starting with the corresponding aromatic halides and hydrogen [ 11C]cyanide, the substituted [ 11C]benzonitriles were prepared using a palladium promoted reaction. Conversion of the nitriles to [carboxy- 11C]amides was achieved by reaction with sodium percarbonate. A one-pot procedure for the synthesis of the 11C-labelled aromatic amides was developed. The total synthesis time including reversed-phase HPLC purification was 25–35 min. Decay-corrected radiochemical yield was 45–70% and the radiochemical purity < 99%. The specific radioactivity was in the order of 2–3 Ci · μmol −1. Initial distribution and kinetic studies were performed in monkey using the tracer substance injected as a rapid bolus. These studies demonstrated that the blood-clearance was fast for [carboxy- 11C]nicotinamide but considerably slower for 3-amino[carboxy- 11C]benzamide and 3-methoxy[carboxy- 11C]benzamide. The brain uptake was low for all substances except 3-methoxy[carboxy- 11C]benzamide which initially had a high brain uptake, followed by a rapid wash out. The 11C-labelled nicotinamide demonstrated a rapid fixation with high uptake values in the liver, kidney and lymph nodes.