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A Novel Method for Direct site-specific Radiolabeling of Peptides Using [(18)F]FDG
We have used the well-accepted and easily available 2-[(18)F]Fluoro-2-deoxyglucose ([(18)F]FDG) positron emission tomography (PET) tracer as a prosthetic group for synthesis of (18)F-labeled peptides. We herein report the synthesis of [(18)F]FDG-RGD ((18)F labeled linear RGD) and [(18)F]FDG-cyclo(RG...
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| Hauptverfasser: | , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2009
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2765576/ https://ncbi.nlm.nih.gov/pubmed/19226160 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bc800422b |
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