Four 1251-labelled nicotine analogs were synthesized: 3-(methylpropylaminomethyl)-, 3-(diethylaminomethyl)-, 3-(isopropylaminomethy1)-, and 3-(diisopropylaminomethy1)-5-[ 1251]-iodopyridines. 5-Bromonicotinic acid was acylated with thionyl chloride and then reacted with the appropriate primary and s
Synthesis and biodistribution of radioiodinated-5-iodonicotine
✍ Scribed by S. M. Chan; G. P. Basmadjian; D. F. Marten; S. A. Sadek; R. A. Magarian; J. R. Grunder; R. D. Ice
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- French
- Weight
- 327 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
5‐Bromonicotine, synthesized from nicotinic acid, was autoclaved with Na^125^I in the presence of copper sulfate and glacial acetic acid to give 5‐[^125^I]iodonicotine. The radiochemical yield was 25.3%. The specific activity of the product was approximately 61 mCi/mmole. Biodistribution studies of 5‐[^125^I]iodonicotine, performed in rats, showed that the labelled compound accummulated rapidly in the brain and the adrenal gland. The highest uptake of radioactivity in these organs occurred at 5 minutes after administration. The brain‐to‐blood and the adrenal‐to‐blood ratios at this time interval were 2.6:1 and 3.3:1 respectively.
📜 SIMILAR VOLUMES
## S W R Y (2-[ lZ5I ]iodobenzyl)benzylmethylselenonium tetraf luoroborate (L) and (0-[ 1251]iodobenzyl)dibenzylselenonium tetrafluor b rate (2) were synthesized by methylation and benzylation of ~-[PzPI]iodobenzyl benzyl selenide respectively. The starting compound 2-iodobenzyl benzyl selenide wa
## Abstract Baclofen has been found to bind to receptors in the central nervous system that are specific for γ‐aminobutyric acid (GABA), a well known inhibitory neurotransmitter. This paper describes the synthesis of a radioiodinated analog of baclofen as part of an effort to develop receptor probe
## Abstract Acetyl‐3,5‐Br‐82‐dibromosalicylic acid (dibromoaspirin) was synthesized by radiobromination of salicylic acid to yield 3,5‐dibromosalicylic acid, followed by acetylation of this intermediate. Biodistribution studies in mice with and without a neuroblastoma showed that the tumor/blood ra