Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10916019 | Nuclear Medicine and Biology | 2014 | 7 Pages |
Abstract
These studies have demonstrated that compounds based on [18F]flumazenil, but with alterations to allow improved radiosynthesis, can be prepared which have ideal properties and warrant further evaluation as PET agents for the GABAA receptor. In particular, compounds 3 and 5 show very promising profiles with specific binding and in vivo stability comparable to flumazenil.
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Authors
Alexander Jackson, Mark R. Battle, Dennis M. O'Shea, Wai-Fung Chau, Alessandra Gaeta, Samantha L. Brown, Amanda L. Ewan, Clare L. Jones, Paul A. Jones, John L. Woodcraft, Denis R. Bouvet, Benedicte B. Guilbert, William Trigg,