14 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
26200936	39	Applications of Fluorine in Medicinal Chemistry.	Bristol-Myers Squibb Research and Development
23306054	1	Probing the steric requirements of the¿-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin.	Northwestern University
22944334	9	Synthesis and evaluation of novel heteroaromatic substrates of GABA aminotransferase.	Northwestern University
3761305	3	Inactivation of gamma-aminobutyric acid aminotransferase by (S,E)-4-amino-5-fluoropent-2-enoic acid and effect on the enzyme of (E)-3-(1-aminocyclopropyl)-2-propenoic acid.	TBA
	5	-Amino acid analogues as mechanism-based inactivators of -aminobutyric acid aminotransferase	TBA
17149870	6	Fluorinated conformationally restricted gamma-aminobutyric acid aminotransferase inhibitors.	Northwestern University
14640537	2	Design, synthesis, and biological activity of a difluoro-substituted, conformationally rigid vigabatrin analogue as a potent gamma-aminobutyric acid aminotransferase inhibitor.	Northwestern University
10691696	14	A new class of conformationally rigid analogues of 4-amino-5-halopentanoic acids, potent inactivators of gamma-aminobutyric acid aminotransferase.	Northwestern University
10579835	6	Inhibition and substrate activity of conformationally rigid vigabatrin analogues with gamma-aminobutyric acid aminotransferase.	Northwestern University
9925739	2	2,6-Difluorophenol as a bioisostere of a carboxylic acid: bioisosteric analogues of gamma-aminobutyric acid.	Northwestern University
8576911	4	Slow-binding inhibition of gamma-aminobutyric acid aminotransferase by hydrazine analogues.	Northwestern University
3701787	4	4-Amino-2-(substituted methyl)-2-butenoic acids: substrates and potent inhibitors of gamma-aminobutyric acid aminotransferase.	TBA
2308143	2	Selective inhibition of gamma-aminobutyric acid aminotransferase by (3R,4R),(3S,4S)- and (3R,4S),(3S,4R)-4-amino-5-fluoro-3-phenylpentanoic acids.	Northwestern University