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Nuclear medicine progress report for quarter ending December 31, 1986

Technical Report ·
OSTI ID:6220125

The synthesis of the 4,4'-dimethyl analogue of the model 3,3'-dimethyl fatty acid, 15-(p-iodophenyl)-3,3-dimethylpentadecanoic acid (3,3'-DMIPP), is described. The (I-125) labeled 4,4'-DMIPP was evaluated in fasted rats and surprisingly showed higher myocardial uptake and faster blood clearance than the 3,3'-, 6,6'- and 9,9'-DMIPP analogues (heart(heart:blood), % dose/gm, 30 min: 3,3' = 5.06 (12:1), 4,4' = 8.03 (16.7:1), 6,6' = 2.26 (3.1:1), 9,9'= 3.06 (2.77)). Since all analogues have the same chain length, differences in tissue uptake and clearance apparently result from the position of geminal dimethyl-branching. This report describes the development of a ''kit'' for the rapid, one-step radioiodination of N-(p-iodophenyl)maleimide. This work involved the coupling of 4-aminophenylmercuric acetate with maleic anhydride to give the acid amide which was then ring annulated with sodium acetate to give the N-(p-acetylmercuricphenyl)maleimide ''kit.'' The crystalline kit is readily radioiodinated with /*I)I/sub 2/ to give the N-(p-iodophenyl)maleimide protein labeling agent. Shipments of research products were made to medical cooperative programs. 2 refs., 5 figs., 1 tab.

Research Organization:
Oak Ridge National Lab., TN (USA)
DOE Contract Number:
AC05-84OR21400
OSTI ID:
6220125
Report Number(s):
ORNL/TM-10377; ON: DE87011952
Country of Publication:
United States
Language:
English

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