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  • Synthesis and screening of mono- and di-aryl technetium and rhenium metallocarboranes. A new class of probes for the estrogen receptor.

Synthesis and screening of mono- and di-aryl technetium and rhenium metallocarboranes. A new class of probes for the estrogen receptor.

Journal of medicinal chemistry (2008-04-17)
Patrick W Causey, Travis R Besanger, John F Valliant
ABSTRACT

A series of mono and diaryl rhenium(I)-carborane derivatives were prepared using microwave heating and screened for their affinity for two isoforms of the estrogen receptor (ER). The rhenacarborane derivative [(RR'C 2B9H9)Re(CO)3](-) (R = p-PhOH, R' = H), which was generated by taking advantage of a recently discovered cage isomerization process, and the neutral nitrosated analogue [(RR'C2B9H9)Re(CO)2(NO)] (R = p-PhOH, R' = H) showed the highest affinities of the compounds screened. As a result, the (99m)Tc analogue of one of the leads was produced in high yield (84%) and specific activity in a manner that is suitable for routine production in support of future preclinical and molecular imaging studies.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
4-Phenylphenol, purified by sublimation, 99%
Supelco
Pentachlorophenol solution, certified reference material, 5000 μg/mL in methanol
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o-Cresol, analytical standard
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p-Cresol, analytical standard
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Pentachlorophenol, 97%
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4-Phenylphenol, 97%
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o-Cresol, ReagentPlus®, ≥99%
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p-Cresol, 99%
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Phenol, unstabilized, purified by redistillation, ≥99%
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