The preparation of the 61-specific ligand 7-benzylidenenaltrexone (BNTX), labeled with tritium at high specific activity (14.4 Ciimmol) was prepared in 33% yield and >98% purity by the aldol condensation of high specific activity [15,1 6-3H]naltrexone with benzaldehyde at high dilution.
Biosynthesis of [7-3H]16α-hydroxy-dehydroepiandrosterone having high specific activity
✍ Scribed by Dr. M. Iida; Dr. K. Matsuhashi; T. Nakayama
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 280 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0233-111X
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✦ Synopsis
Abstract
Biosynthesis of [7‐^3^H]16α‐hydroxy‐dehydroepiandrosterone in high specific activity has been studied. [7‐^3^H] dehydroepiandrosterone (13.9 C/mM) in trace quantity was oxidized by Streptomyces roseochromogenes (NRRLB‐1233) for 5 min at 27 °C. The radioactive products were chromatographically separated, identified and their radiochemical purity established by isotopic dilution analysis. [7‐^3^H]16α‐hydroxy‐dehydroepiandrosterone (2.5 × 10^7^ dpm) was obtained by microbial hydroxylation of substrate (1.9 × 10^9^ dpm). In some cases [7‐^3^H]5‐androstene‐3β, 16α, 17β‐triol in a small amount of radioactivity could be found at the prolonged reaction for 30 hr.
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