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Blockade of the brain histamine H3 receptor by JNJ-39220675: preclinical PET studies with [(11)C]GSK189254 in anesthetized baboon

RATIONALE: The preclinical characterization of a series of aryloxypyridine amides has identified JNJ-39220675 ((4-cyclobutyl-1,4-diazepan-1-yl)(6-(4-fluorophenoxy)pyridin-3-yl)methanone) as a high-affinity histamine H(3) receptor antagonist and a candidate for further drug development particularly i...

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Hlavní autoři: Logan, Jean, Carruthers, Nicholas I., Letavic, Michael A., Sands, Steven, Jiang, Xiaohui, Shea, Colleen, Muench, Lisa, Xu, Youwen, Carter, Pauline, King, Payton, Fowler, Joanna S.
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer-Verlag 2012
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3456925/
https://ncbi.nlm.nih.gov/pubmed/22614669
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00213-012-2733-x
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