PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8147263-8	1993	However, enzyme kinetic experiments showed that pargyline, like many other amines, was a competitive inhibitor of HNMT.	Amines	75-81	histamine N-methyltransferase	Homo sapiens	114-118	
7976798-8	1994	Inhibitors of histamine-N-methyltransferase diminished the elimination rate of both amines studied.	Amines	84-90	histamine N-methyltransferase	Homo sapiens	14-43	
8147263-13	1993	Finally, several amine compounds related structurally to pargyline were also found to be inhibitors of HNMT.	Amines	17-22	histamine N-methyltransferase	Homo sapiens	103-107	
21036620-2	2010	To obtain novel inhibitors as tools for investigating the physiological function of members of the HMT family, we designed and synthesized novel inhibitors, which are amine analogues of adenosylmethionine (AdoMet; the cofactor utilized in the methylation reaction) bearing various alkylamino groups coupled via an ethylene linker.	Amines	167-172	histamine N-methyltransferase	Homo sapiens	99-102	
2958359-1	1987	The concentrations of serotonin, tryptamine, dopamine, and tyramine were quantitatively determined in the Arthus reaction, since the activity of histamine-N-methyltransferase (HMT), a major histamine-metabolizing enzyme that had been demonstrated to be inhibited by such biogenic amines in vitro, decreased significantly in the reaction site.	Amines	280-286	histamine N-methyltransferase	Homo sapiens	176-179	
12417108-1	2002	BACKGROUND: Histamine N-methyltransferase (HNMT) plays an important role in the metabolism of histamine, a biogenic amine that has many physiologic and pathological roles in human tissues.	Amines	16-21	histamine N-methyltransferase	Homo sapiens	43-47