gabaculine

Known as: 3-amino-2,3-dihydrobenzoic acid, 5-amino-1,3-cyclohexadienylcarboxylic acid, gabaculin 
 
National Institutes of Health

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2007
2007
PURPOSE gamma-Aminobutyric acid (GABA) and N-methyl-D-aspartate (NMDA) receptors are important targets for anesthetic action at… (More)
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2004
2004
Deletion of the genes for four or five small Cab-like proteins (SCPs) in photosystem (PS) I-less and PS I-less/PS II-less strains… (More)
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Highly Cited
1997
Highly Cited
1997
This study was conducted to determine whether endogenous synthesis of arginine plays a role in regulating arginine homeostasis in… (More)
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1989
1989
Gabaculine, a potent suicide inhibitor of ornithine aminotransferase (OAT), at a dose of 50 mg/kg inhibited this enzyme in mouse… (More)
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1988
1988
The potassium-stimulated release of gamma-aminobutyric acid (GABA) from synaptosomes was determined in preparations from control… (More)
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1988
1988
Glutamic acid 1-semialdehyde hydrochloride was synthesized and purified. Its prior structural characterization was extended and… (More)
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1985
1985
Gabaculine (5-amino-1,3-cyclohexadienylcarboxylic acid), a transaminase inhibitor, also inhibits chlorophyll formation in plants… (More)
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Highly Cited
1985
Highly Cited
1985
Both mono-and dicotyledonous species catabolize putrescine to γ-aminobutyric acid (GABA), but by two different pathways. GABA is… (More)
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1982
1982
The turnover and release of endogenous and labeled GABA were followed in rat cortical slices after incubation with [3H]GABA. High… (More)
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1977
1977
Gabaculine (5-amino-1,3-cyclohexadienylcarboxylic acid), a naturally occurring amino acid isolated from Streptomyces toyacaenis… (More)
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