The preparation of tritiated E- and Z-4-aminobut-2-enoic acids, conformationally restricted analogues of the inhibitory neurotransmitter 4-aminobutanoic acid (GABA)
- 1 June 1993
- journal article
- research article
- Published by Wiley in Journal of Labelled Compounds and Radiopharmaceuticals
- Vol. 33 (6) , 527-540
- https://doi.org/10.1002/jlcr.2580330610
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Bicuculline‐ and Baclofen‐Insensitive γ‐Aminobutyric Acid Binding to Rat Cerebellar MembranesJournal of Neurochemistry, 1992
- Synthesis of Analogues of GABA. XIII. An Alternative Route to (Z)-4-Aminocrotonic AcidAustralian Journal of Chemistry, 1985
- Bicuculline-insensitive GABA receptors: Studies on the binding of (−)-baclofen to rat cerebellar membranesNeuroscience Letters, 1984
- GABA agonistsNeuropharmacology, 1984
- Synthetic analogs for the study of GABA as a neurotransmitterMedicinal Research Reviews, 1983
- 3H-baclofen and 3H-GABA bind to bicuculline-insensitive GABAB sites in rat brainNature, 1981
- The Synthesis and Activity of cis‐and trans‐2‐(Aminomethyl) cyclopropanecarboxylic Acid as Conformationally Restricted Analogues of GABAJournal of Neurochemistry, 1980
- Synthesis of some substituted 4-Aminobut-2-enoic acids as analogues of the neurotransmitter GABAAustralian Journal of Chemistry, 1978
- CIS‐ AND TRANS‐4‐AMINOCROTONIC ACID AS GABA ANALOGUES OF RESTRICTED CONFORMATIONJournal of Neurochemistry, 1975
- Biosynthesis of plant sterols—IV. , An investigation of a possible mode of 14β-hydroxylation in digitoxigeninPhytochemistry, 1968