Synthesis of Analogues of GABA. XIV. Synthesis and Activity of Unsaturated Derivatives of 5-Aminopentanoic Acid (d-Aminovaleric Acid)
- 1 January 1985
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 38 (11), 1651-1656
- https://doi.org/10.1071/ch9851651
Abstract
The (Z) and (E) pairs of 5-aminopent-2-enoic acid and 5-aminopent-3- enoic acid, as well as the related 5-aminopent-3-ynoic acid, have been prepared for structure-activity studies on GABA receptors. Only the (Z) isomers were active as GABA agonists with (Z)-5-aminopent-2-enoic acid being two- to four-fold more active than 5-aminopentanoic acid.Keywords
This publication has 3 references indexed in Scilit:
- Evidence that ethylenediamine acts in the isolated ileum of the guinea-pig by releasing endogenous GABABritish Journal of Pharmacology, 1984
- Actions of pentobarbitone and derivatives with modified 5-butyl substituents on GABA and diazepam binding to rat brain synaptosomal membranesNeurochemical Research, 1983
- GABA Induced excitatory responses in the guinea-pig small intestine are antagonized by bicuculline, picrotoxinin and chloride ion blockersNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1981