Feasibility of a stereoselective synthesis of [11C](S, S)-S-adenosylmethionine ([11C](S,S)-SAM) catalyzed by an immobilized enzyme
This work aims to develop a stereoselective enzymatic alternative for the radiosynthesis of [11C](S,S)-S-ade-nosylmethionine ([11C](S,S)-SAM), a potential PET-CT radiotracer for monitoring particularly aggressive prostate tumors. Conventional synthesis of this compound has been carried out at Urugua...
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| Další autoři: | , , , , , |
| Médium: | article |
| Jazyk: | angličtina |
| Vydáno: |
2024
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| Témata: | |
| On-line přístup: | https://hdl.handle.net/20.500.12381/5578 https://doi.org/10.1016/j.procbio.2024.12.006 |
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