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14 articles for thisTarget


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

PMID
Data
Article Title
Organization
Applications of Fluorine in Medicinal Chemistry.EBI
Bristol-Myers Squibb Research and Development
Probing the steric requirements of the¿-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin.EBI
Northwestern University
Synthesis and evaluation of novel heteroaromatic substrates of GABA aminotransferase.EBI
Northwestern University
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.EBI
TBA
 
-Amino acid analogues as mechanism-based inactivators of -aminobutyric acid aminotransferaseEBI
TBA
Fluorinated conformationally restricted gamma-aminobutyric acid aminotransferase inhibitors.EBI
Northwestern University
Design, synthesis, and biological activity of a difluoro-substituted, conformationally rigid vigabatrin analogue as a potent gamma-aminobutyric acid aminotransferase inhibitor.EBI
Northwestern University
Mechanism-Based Design of 3-Amino-4-Halocyclopentenecarboxylic Acids as Inactivators of GABA Aminotransferase.EBI
Northwestern University
A new class of conformationally rigid analogues of 4-amino-5-halopentanoic acids, potent inactivators of gamma-aminobutyric acid aminotransferase.EBI
Northwestern University
Inhibition and substrate activity of conformationally rigid vigabatrin analogues with gamma-aminobutyric acid aminotransferase.EBI
Northwestern University
2,6-Difluorophenol as a bioisostere of a carboxylic acid: bioisosteric analogues of gamma-aminobutyric acid.EBI
Northwestern University
Slow-binding inhibition of gamma-aminobutyric acid aminotransferase by hydrazine analogues.EBI
Northwestern University
4-Amino-2-(substituted methyl)-2-butenoic acids: substrates and potent inhibitors of gamma-aminobutyric acid aminotransferase.EBI
TBA
Selective inhibition of gamma-aminobutyric acid aminotransferase by (3R,4R),(3S,4S)- and (3R,4S),(3S,4R)-4-amino-5-fluoro-3-phenylpentanoic acids.EBI
Northwestern University