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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Autores principales: Namavari, Mohammad, Cheng, Zhen, Zhang, Rong, De, Abhijit, Levi, Jelena, Hoerner, Joshua K., Yaghoubi, Shahriar S., Syud, Faisal A., Gambhir, Sanjiv S.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2009
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Article
Acceso en línea: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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