PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17348765-3	2007	The first-generation MAOIs such as phenelzine and isocarboxazid were largely nonselective inhibitors of both subtypes of MAO, MAO(A) and MAO(B).	Phenelzine	35-45	monoamine oxidase B	Homo sapiens	137-143	
18426226-4	2008	Phenylethylhydrazine stoichiometrically reduces the covalent FAD moieties of MAO A and of MAO B.	Phenelzine	0-20	monoamine oxidase B	Homo sapiens	90-95	
18426226-5	2008	Molecular oxygen is required for the inhibition reactions, and the level of O2 consumption for phenylethylhydrazine is 6-7-fold higher with either MAO A or MAO B than for the corresponding reactions with benzylhydrazine or phenylhydrazine.	Phenelzine	95-115	monoamine oxidase B	Homo sapiens	156-161	
18426226-8	2008	The three-dimensional (2.3 A) structures of phenylethylhydrazine- and benzylhydrazine-inhibited MAO B show that alkylation occurs at the N(5) position on the re face of the covalent flavin with loss of the hydrazyl nitrogens.	Phenelzine	44-64	monoamine oxidase B	Homo sapiens	96-101	
9829163-3	1998	While the classical, nonselective and nonreversible MAOIs, such as phenelzine and tranylcypromine, are characterised by the risk of inducing a hypertensive crisis when dietary tyramine is ingested, the selective monoamine oxidase-B (MAO-B) inhibitor selegiline (deprenyl) and, even more so, the selective and reversible monoamine oxidase-A (MAO-A) inhibitor moclobemide, are free from this potential interaction.	Phenelzine	67-77	monoamine oxidase B	Homo sapiens	212-231	
9829163-3	1998	While the classical, nonselective and nonreversible MAOIs, such as phenelzine and tranylcypromine, are characterised by the risk of inducing a hypertensive crisis when dietary tyramine is ingested, the selective monoamine oxidase-B (MAO-B) inhibitor selegiline (deprenyl) and, even more so, the selective and reversible monoamine oxidase-A (MAO-A) inhibitor moclobemide, are free from this potential interaction.	Phenelzine	67-77	monoamine oxidase B	Homo sapiens	233-238	
30242487-2	2018	The monoamine oxidases A and B (MAOA/MAOB) are prime candidates for the investigation into the role of DNA methylation in mental disorders, given their pivotal role in the metabolism of monoamines and as pharmacological targets of potent antidepressant drugs such as tranylcypromine, phenelzine or moclobemide.	Phenelzine	284-294	monoamine oxidase B	Homo sapiens	37-41