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・ Beta-2 transferrin
・ Beta-2-Thienylalanine
・ Beta-3 adrenergic receptor
・ Beta-actin
・ Beta-adrenergic agonist
・ Beta-adrenergic-receptor kinase
・ Beta-Ala-His dipeptidase
・ Beta-Alanine
・ Beta-alanine aminotransferase
・ Beta-Alanine ethyl ester
・ Beta-alanine—pyruvate transaminase
・ Beta-alanopine dehydrogenase
・ Beta-alanyl-CoA ammonia-lyase
・ Beta-alumina solid electrolyte
・ Beta-Amanitin
Beta-Aminobutyric acid
・ Beta-amyrin 11-oxidase
・ Beta-amyrin 24-hydroxylase
・ Beta-amyrin synthase
・ Beta-apiosyl-beta-glucosidase
・ Beta-apo-4'-carotenal oxygenase
・ Beta-Araneosene
・ Beta-aspartyl-N-acetylglucosaminidase
・ Beta-aspartyl-peptidase
・ Beta-binomial distribution
・ Beta-Bungarotoxin
・ Beta-Carboline
・ Beta-Carotene
・ Beta-carotene 15,15'-dioxygenase
・ Beta-carotene 15,15'-monooxygenase


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Beta-Aminobutyric acid : ウィキペディア英語版
Beta-Aminobutyric acid

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β-Aminobutyric acid (BABA) is an isomer of the amino acid aminobutyric acid with the chemical formula C4H9NO2. It has two isomers, alpha-aminobutyric acid and gamma-aminobutyric acid (GABA), a neurotransmitter in animals that is also found in plants, where it may play a role in signalling. All three are non-proteinogenic amino acids, not being found in proteins. BABA is known for its ability to induce plant disease resistance, as well as increased resistance to abiotic stresses, when applied to plants.
==Synthesis==
Methods to synthesise BABA are known from at least 1857. Early methods to produce BABA included from ammonia and crotonic acid under pressure; from the acetoacetic ester phenylhydrazone; or from malonic acid, acetaldehyde, and ammonia. In 1957, Zilkha reported a new simpler method based on adding amines to crotonic acid and then catalytically hydrogenolysing the product to produce BABA.〔(【引用サイトリンク】title=3-aminobutanoic acid )〕 Since 2000, methods to produce only the ''S'' stereoisomer of BABA have also been reported.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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