Cat. No. 0796
Alternative Name: STX 209
Chemical Name: (R)-4-Amino-3-(4-chlorophenyl)butan
Biological ActivityMore active enantiomer of (RS)-Baclofen (Cat. No. 0417), a selective GABAB agonist.
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Safety Data Sheet
Hong et al (1991) Effects of phaclofen and the enantiomers of baclofen on cardiovascular responses to intrathecal administration of L- and D-baclofen in the rat. Eur.J.Pharmacol. 196 267. PMID: 1654254.
Falch et al (1986) Comparative stereostructure-activity studies on GABAA and GABAB receptor sites and GABA uptake using rat brain membrane preparations. J.Neurochem. 47 898. PMID: 3016189.
If you know of a relevant reference for this product please let us know.
Citations are publications that use Tocris products. Selected citations for (R)-Baclofen include:
Bragina et al (2015) Differential expression of metabotropic glutamate and GABA receptors at neocortical glutamatergic and GABAergic axon terminals. Front Cell Neurosci 9 345. PMID: 26388733.
Xia et al (2014) Regulation of action potential waveforms by axonal GABAA receptors in cortical pyramidal neurons. PLoS One 9 e100968. PMID: 24971996.
Hensler et al (2012) GABAB receptor-positive modulators: brain region-dependent effects. J Pharmacol Exp Ther 340 19. PMID: 21954301.
Bartoi et al (2010) GABAB receptor constituents revealed by tandem affinity purification from transgenic mice. J Biol Chem 285 20625. PMID: 20406808.
Lobb et al (2010) A dynamic role for GABA receptors on the firing pattern of midbrain dopaminergic neurons. J Neurophysiol 104 403. PMID: 20445035.
Piqueras and Martínez (2004) Peripheral GABAB agonists stimulate gastric acid secretion in mice. Br J Pharmacol 142 1038. PMID: 15210585.
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Keywords: (R)-Baclofen, supplier, Selective, GABAB, agonists, Receptors, STX209, Tocris Bioscience, GABAB Receptor Agonist products
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