Synthesis and evaluation of candidate PET radioligands for corticotropin-releasing factor type-1 receptors
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Don't stress about CRF: assessing the translational failures of CRF1antagonists.Synthesis, F-18 radiolabeling, and microPET evaluation of 3-(2,4-dichlorophenyl)-N-alkyl-N-fluoroalkyl-2,5-dimethylpyrazolo[1,5-a]pyrimidin-7-amines as ligands of the corticotropin-releasing factor type-1 (CRF1) receptor.Failed PET Application Attempts in the Past, Can We Avoid Them in the Future?The CRF System as a Therapeutic Target for Neuropsychiatric Disorders.Synthesis, binding affinity, radiolabeling, and microPET evaluation of 4-(2-substituted-4-substituted)-8-(dialkylamino)-6-methyl-1-substituted-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-ones as ligands for brain corticotropin-releasing factor type-1 (CRFFluorine-18 labelled building blocks for PET tracer synthesis.Imaging corticotropin-releasing-factor and nociceptin in addiction and PTSD models.
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Synthesis and evaluation of candidate PET radioligands for corticotropin-releasing factor type-1 receptors
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name
Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Synthesis and evaluation of ca ...... easing factor type-1 receptors
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Douglas D Dischino
Frederick T Chin
Heidi Dulac
Jeffrey A Deskus
Joanne J Bronson
John E Macor
Masahiro Fujita
Masao Imaizumi
Nicholas J Lodge
Rick Pieschl
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P304
P356
10.1016/J.NUCMEDBIO.2014.03.005
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2014-03-29T00:00:00Z