4-aminobutyrate aminotransferase
Encyclopedia
4-aminobutyrate aminotransferase (or GABA transaminase) is an enzyme which catalyzes the conversion of 4-aminobutanoic acid (GABA) and 2-oxoglutarate into succinic semialdehyde
Succinic semialdehyde
Succinic semialdehyde is a GABA analogue.-See also:* Succinic semialdehyde dehydrogenase deficiency* 4-aminobutyrate aminotransferase...

 and glutamate.

Inhibitors

  • Aminooxyacetic acid
    Aminooxyacetic acid
    Aminooxyacetic acid, often abbreviated AOA or AOAA, is a compound that inhibits 4-aminobutyrate aminotransferase activity in vitro and in vivo, leading to less gamma-aminobutyric acid being broken down. Subsequently, the level of GABA is increased in tissues...

  • Gabaculine
    Gabaculine
    Gabaculine is a naturally occurring neurotoxin first isolated from the bacteria Streptomyces toyacaensis, which acts as a potent and irreversible GABA transaminase inhibitor, and also a GABA reuptake inhibitor....

  • Phenelzine
    Phenelzine
    Phenelzine is a non-selective and irreversible monoamine oxidase inhibitor of the hydrazine class which is used as an antidepressant and anxiolytic...

  • Phenylethylidenehydrazine
    Phenylethylidenehydrazine
    Phenylethylidenehydrazine is an inhibitor of the enzyme GABA transaminase . It is a metabolite of the antidepressant phenelzine and is responsible for its elevation of GABA concentrations. PEH likely plays a significant role in phenelzine's high efficacy in treating anxiety disorders....

     (PEH)
  • Valproic acid
    Valproic acid
    Valproic acid is a chemical compound that has found clinical use as an anticonvulsant and mood-stabilizing drug, primarily in the treatment of epilepsy, bipolar disorder, and, less commonly, major depression. It is also used to treat migraine headaches and schizophrenia...

  • Vigabatrin
    Vigabatrin
    Vigabatrin is an antiepileptic drug that inhibits the catabolism of gamma-aminobutyric acid by irreversibly inhibiting GABA transaminase. It is an analog of GABA, but it is not a receptor agonist...

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