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Convenient Synthesis of (18)F-Radiolabeled R-(−)-N-n-propyl-2-(3-fluoropropanoxy-11-hydroxynoraporphine
Aporphines are attractive candidates for imaging D(2) receptor function because, as agonists rather than antagonists, they are selective for the receptor in the high affinity state. In contrast, D(2) antagonists do not distinguish between the high and low affinity states, and in vitro data suggests...
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| Foilsithe in: | J Labelled Comp Radiopharm |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2014
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4275395/ https://ncbi.nlm.nih.gov/pubmed/25400260 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jlcr.3246 |
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