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- Publications
- Influence
Carbon-11-FLB 457: a radioligand for extrastriatal D2 dopamine receptors.
- C. Halldin, L. Farde, +6 authors C. Swahn
- Chemistry, Medicine
- Journal of nuclear medicine : official…
- 1 July 1995
UNLABELLED
D2 dopamine receptors in extrastriatal brain regions are of central interest for research in schizophrenia and antipsychotic drugs. This article reports the development of [11C]FLB 457 for… Expand
Binding characteristics of remoxipride and its metabolites to dopamine D2 and D3 receptors.
- N. Mohell, M. Sällemark, S. Rosqvist, A. Malmberg, T. Hoegberg, D. M. Jackson
- Biology, Medicine
- European journal of pharmacology
- 6 July 1993
The substituted benzamide, remoxipride, is a new atypical antipsychotic agent with good clinical efficacy and low extrapyramidal side-effect potential. In the present study, the in vitro receptor… Expand
Dopamine D2 receptors in the rat, monkey and the post-mortem human hippocampus. An autoradiographic study using the novel D2-selective ligand 125I-NCQ 298
- C. Köhler, H. Ericson, T. Hoegberg, C. Halldin, V. Chan-Palay
- Biology, Medicine
- Neuroscience Letters
- 15 April 1991
The distribution of dopamine D2 receptors in the hippocampal region of the rat, monkey and the postmortem human brain was studied with in vitro receptor autoradiography using the selective… Expand
Synthesis of [methoxy-3H]- and [methoxy-11C]- labelled raclopride. Specific dopamine-D2 receptor ligands
- E. Ehrin, L. Gawell, T. Hoegberg, T. D. Paulis, Peter Ström
- Chemistry
- 1 August 1987
Radioactive labelled raclopride and its (R)-isomer were prepared by O-alkylation of the corresponding phenols with labelled methyl iodide. The syntheses of the two phenolic precursors from (R)- and… Expand
Stereoselective binding of 11C-raclopride in living human brain — a search for extrastriatal central D2-dopamine receptors by PET
- L. Farde, S. Pauli, +6 authors S. Stone-Elander
- Chemistry, Medicine
- Psychopharmacology
- 2004
The selective D2-dopamine receptor antagonist raclopride and its pharmacologically inactive (R)-enantiomer FLB472 were labelled with 11C and used in a study with positron emission tomography to… Expand
New selective dopamine D-2 antagonists as antipsychotic agents. Pharmacological, chemical, structural and theoretical considerations.
- T. Hoegberg, S. Raemsby, S. Ogren, U. Norinder
- Chemistry, Medicine
- Acta pharmaceutica Suecica
- 1987
Structure-activity relationships among DNA gyrase inhibitors. Synthesis and biological evaluation of 1,2-dihydro-4, 4-dimethyl-1-oxo-2-naphthalenecarboxylic acids as 1-carba bioisosteres of oxolinic…
- T. Hoegberg, I. Khanna, S. D. Drake, L. Mitscher, L. L. Shen
- Chemistry, Medicine
- Journal of medicinal chemistry
- 1 March 1984
A series of oxolinic acid analogues was synthesized in an attempt to evaluate the role, if any, played by the N-1 atom in putative modes of action of antimicrobial DNA gyrase inhibitors. Carba… Expand
Potential antipsychotic agents 5. Synthesis and antidopaminergic properties of substituted 5,6-dimethoxysalicylamides and related compounds.
- T. Hoegberg, Stefan Bengtsson, +4 authors S. O. Ógren
- Chemistry, Medicine
- Journal of medicinal chemistry
- 1 April 1990
A series of 3-substituted 5,6-dimethoxysalicylamides III (9-13 and 15) has been synthesized from the corresponding 2,5,6-trimethoxybenzoic acids. Relaxation times T1 and carbon chemical shifts of the… Expand
Single-pulse laser-induced OH fluorescence in an atmospheric flame, spatially resolved with a diode array detector.
- M. Aldén, H. Edner, G. Holmstedt, S. Svanberg, T. Hoegberg
- Materials Science, Medicine
- Applied optics
- 1 April 1982
Laser-induced fluorescence measurements of OH have been performed in an atmospheric stoichiometric CH(4)/air flame and in a highly sooting propane flame. The measurements were realized with a single… Expand
Semisynthesis of Ingenol 3-Angelate (PEP005): Efficient Stereoconservative Angeloylation of Alcohols
- Liang Xi-fu, Gunnar Grue-Sørensen, A. K. Petersen, T. Hoegberg
- Chemistry
- 18 October 2012
A high-yielding method was developed for the preparation of ingenol 3-angelate (PEP005, ingenol mebutate) via the corresponding 5,20-acetonide without concomitant isomerization of the angelate… Expand