PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23306054-1	2013	We have synthesized three analogues of 4-amino-5-fluorohexanoic acids as potential inactivators of gamma-aminobutyric acid aminotransferase (GABA-AT), which were designed to combine the potency of their shorter chain analogue, 4-amino-5-fluoropentanoic acid (AFPA), with the greater enzyme selectivity of the antiepileptic vigabatrin (Sabril ).	4-amino-5-fluorohexanoic acids	39-69	4-aminobutyrate aminotransferase	Homo sapiens	99-139
23306054-1	2013	We have synthesized three analogues of 4-amino-5-fluorohexanoic acids as potential inactivators of gamma-aminobutyric acid aminotransferase (GABA-AT), which were designed to combine the potency of their shorter chain analogue, 4-amino-5-fluoropentanoic acid (AFPA), with the greater enzyme selectivity of the antiepileptic vigabatrin (Sabril ).	4-amino-5-fluorohexanoic acids	39-69	4-aminobutyrate aminotransferase	Homo sapiens	141-148