Cargando…
Sweetening Pharmaceutical Radiochemistry by (18)F-Fluoroglycosylation: Recent Progress and Future Prospects
In the field of (18)F-chemistry for the development of radiopharmaceuticals for positron emission tomography (PET), various labeling strategies by the use of prosthetic groups have been implemented, including chemoselective (18)F-labeling of biomolecules. Among those, chemoselective (18)F-fluoroglyc...
Autores principales: | Shinde, Sandip S., Maschauer, Simone, Prante, Olaf |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621802/ https://www.ncbi.nlm.nih.gov/pubmed/34832957 http://dx.doi.org/10.3390/ph14111175 |
Ejemplares similares
-
Sweetening Pharmaceutical Radiochemistry by (18)F-Fluoroglycosylation: A Short Review
por: Maschauer, Simone, et al.
Publicado: (2014) -
Neurotensin analogs by fluoroglycosylation at N(ω)-carbamoylated arginines for PET imaging of NTS1-positive tumors
por: Schindler, Lisa, et al.
Publicado: (2022) -
Recent Trends in Pharmaceutical Radiochemistry for Molecular PET Imaging
por: Prante, Olaf, et al.
Publicado: (2014) -
(18)F-Fluorination Using Tri-Tert-Butanol Ammonium Iodide as Phase-Transfer Catalyst: An Alternative Minimalist Approach
por: Shinde, Sandip S., et al.
Publicado: (2021) -
Recent Advances
of S–(18)F Radiochemistry
for Positron Emission Tomography
por: Deng, Xiaoyun, et al.
Publicado: (2023)