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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Marwick, Katie F. M. Spinaci, Andrea Piras, Monica Pertwee, Roger G. Zanda, Matteo Hardingham, Giles E. Wyllie, David J. A. Zanato, Chiara Pelagalli, Alessia Dall'Angelo, Sergio |
| Copyright Year | 2017 |
| Abstract | We report the synthesis of terminally fluorinated HU-210 and HU-211 analogues (HU-210F and HU-211F, respectively) and their biological evaluation as ligands of cannabinoid receptors (CB1 and CB2) and N-methyl D-aspartate receptor (NMDAR). [18F]-labelled HU-210F was radiosynthesised from the bromo-substituted precursor. In vitro assays showed that both HU-210F and HU-211F retain the potent pharmacological profile of HU-210 and HU-211, suggesting that [18F]-radiolabelled HU-210F and HU-211F could have potential as PET tracers for in vivo imaging. |
| Starting Page | 2086 |
| Ending Page | 2096 |
| Page Count | 11 |
| File Format | HTM / HTML PDF |
| ISSN | 14770520 |
| Volume Number | 15 |
| Issue Number | 9 |
| Journal | Organic & Biomolecular Chemistry |
| DOI | 10.1039/c6ob02796b |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Estrogen receptor Cannabinoid receptor Cannabinoid receptor type 1 Aspartic acid Positron emission tomography HU-210 Dexanabinol Isotopic labeling |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Biochemistry Physical and Theoretical Chemistry |
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