PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15035814-0	2003	Interactions of D-amphetamine with the active site of monoamine oxidase-A.	Dextroamphetamine	16-29	monoamine oxidase A	Homo sapiens	54-73	
12445480-5	2002	The inhibitors, D-amphetamine, harmine, tetrindole, and befloxatone all induce similar (but not identical) changes in the spectrum of MAO A, consistent with stacking of inhibitor with the flavin in the active site.	Dextroamphetamine	16-29	monoamine oxidase A	Homo sapiens	134-139	
12445480-6	2002	D-Amphetamine, harmine, and tetrindole stabilise the semiquinone form of FAD during reduction of MAO A by dithionite and no further reduction of these inhibitor-MAO A complexes has been observed.	Dextroamphetamine	0-13	monoamine oxidase A	Homo sapiens	97-102	
21354322-3	2011	The enzyme is competitively inhibited by hMAO A selective reversible inhibitors with the exception of d-amphetamine where uncompetitive inhibition is exhibited.	Dextroamphetamine	102-115	monoamine oxidase A	Homo sapiens	41-47	
2021654-2	1991	In this study, with use of purified monoamine oxidase A, steady-state data for the inhibition by D-amphetamine of the oxidation of primary amines indicate the possibility of a ternary complex mechanism for monoamine oxidase A also.	Dextroamphetamine	97-110	monoamine oxidase A	Homo sapiens	36-55	
2021654-2	1991	In this study, with use of purified monoamine oxidase A, steady-state data for the inhibition by D-amphetamine of the oxidation of primary amines indicate the possibility of a ternary complex mechanism for monoamine oxidase A also.	Dextroamphetamine	97-110	monoamine oxidase A	Homo sapiens	206-225