| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10593462 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
Based on a favorable balance between CRF-R1 affinity, lipophilicity and metabolic stability, compound 10 was evaluated for potential development as PET radioligand. Compound [18F]10 was prepared with high radiochemical purity and showed promising binding properties in rat brain imaging experiments.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jeffrey A. Deskus, Douglas D. Dischino, Ronald J. Mattson, Jonathan L. Ditta, Michael F. Parker, Derek J. Denhart, Dmitry Zuev, Hong Huang, Richard A. Hartz, Vijay T. Ahuja, Henry Wong, Gail K. Mattson, Thaddeus F. Molski, James E. Jr., Larisa Zueva,
-5-chloro-1-(1-cyclopropyl-2-methoxyethyl)-3-(4-(2-fluoroethoxy)-2,5-dimethyl phenylamino)pyrazin-2(1H)-one: Introduction of N3-phenylpyrazinones as potential CRF-R1 PET imaging agents [18F](R)-5-chloro-1-(1-cyclopropyl-2-methoxyethyl)-3-(4-(2-fluoroethoxy)-2,5-dimethyl phenylamino)pyrazin-2(1H)-one: Introduction of N3-phenylpyrazinones as potential CRF-R1 PET imaging agents](/preview/png/10593462.png)