Unexpectedly high affinity of a novel histamine H3receptor antagonist, GSK239512,in vivoin human brain, determined using PET

Author:

Ashworth S1,Berges A2,Rabiner E A13,Wilson A A4,Comley R A1,Lai R Y K5,Boardley R6,Searle G1,Gunn R N13,Laruelle M13,Cunningham V J137

Affiliation:

1. GlaxoSmithKline Clinical Imaging Centre; London UK

2. GlaxoSmithKline Clinical Pharmacology Modelling & Simulation; Stockley Park UK

3. Department of Medicine; Imperial College; London UK

4. The Centre for Addiction and Mental Health (CAMH); Toronto ON Canada

5. GlaxoSmithKline Neurosciences Discovery Medicine; Harlow UK

6. GlaxoSmithKline Clinical Pharmacology Science & Study Operations; Stevenage UK

7. Aberdeen Biomedical Imaging Centre, Institute of Medical Sciences; University of Aberdeen; Aberdeen UK

Publisher

Wiley

Subject

Pharmacology

Reference37 articles.

1. Population pharmacokinetics: theory and practice;Aarons;Br J Clin Pharmacol,1991

2. The Concise Guide to PHARMACOLOGY 2013/14: Overview;Alexander;Br J Pharmacol,2013

3. Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptor;Arrang;Nature,1983

4. Evaluation of 11C-GSK189254 as a novel radioligand for the H3 receptor in humans using PET;Ashworth;J Nucl Med,2010

5. Beal S Sheiner LB 1998 NONMEM User Guides (Nonmem Project Group)

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