Synthesis of (±)-[ 18F]BMY 14802, its enantiomers and their anatomical distributions in rodents
A potential antipsychotic drug, BMY 14802 was labeled with 18F and its distribution in rodents was studied. No-carrier-added (NCA) (±)-[ 18F]BMY 14802 (5) was synthesized by two methods in 5–10% radiochemical yield in a synthesis time of 130–140 min from EOB with a specific activity of 0.5–1.5 Ci/μM...
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Published in | Nuclear medicine and biology Vol. 20; no. 5; pp. 625 - 630 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Inc
01.07.1993
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | A potential antipsychotic drug, BMY 14802 was labeled with
18F and its distribution in rodents was studied. No-carrier-added (NCA) (±)-[
18F]BMY 14802 (5) was synthesized by two methods in 5–10% radiochemical yield in a synthesis time of 130–140 min from EOB with a specific activity of 0.5–1.5 Ci/μM. (+)- and (−)-[
18F]BMY 14802 was synthesized by the chiral reduction of α-(4-[
18F] fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-1-piperazine-butanone (4) with chiral reducing agent, (+)- and (−)-β-chlorodi-isopinocampheylborane [(+)- and (−)-DIP chloride] in 6–10% radiochemical yield in a synthesis time of 150 min from EOB. Animal studies in mouse and in rat revealed that the distribution of 5 in each tissue was high at 5 min, the radioactivity then declined rapidly in all tissues studied except in the liver and in the small intestine. The radioactivity in the femur did not increase with time indicating
in vivo defluorination may not occur. The uptakes of (±)-[
18F]BMY 14802 and its enantiomers, (+)- and (−)-[
18F]BMY 14802 in rat cerebellum, brain stem, hippocampus and spinal cord were similar and were significantly reduced by prior treatment of rat with haldol. This suggests that (±)-[
18F]BMY 14802 and its enantiomers bind to σ-receptors in a similar fashion. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0969-8051 1872-9614 |
DOI: | 10.1016/0969-8051(93)90031-O |