PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15755651-3	2005	Unlike the parent 1-phenylcyclopropylamine, which is a selective inhibitor of MAO B, both (E)- and (Z)-diastereomers of derivatives having fluorine at the 2-position of the cyclopropane ring were potent and selective irreversible inhibitors of MAO A.	1-phenylcyclopropylamine	18-42	monoamine oxidase B	Homo sapiens	78-83	
11331009-1	2001	The spectral properties of the covalent adduct formed between the flavin cofactor of MAO N and 1-PCPA are similar to those reported for the irreversible inactivation product formed with 1-PCPA and mammalian mitochondrial monoamine oxidase B [Silverman, R. B., and Zieske, P. A.	1-phenylcyclopropylamine	95-101	monoamine oxidase B	Homo sapiens	221-240	
3242595-0	1988	Inactivation of monoamine oxidase A by the monoamine oxidase B inactivators 1-phenylcyclopropylamine, 1-benzylcyclopropylamine, and N-cyclopropyl-alpha-methylbenzylamine.	1-phenylcyclopropylamine	76-100	monoamine oxidase B	Homo sapiens	43-62	
3242595-9	1988	The results with 1-PCPA indicate that the active site topographies of MAO A and MAO B are different.	1-phenylcyclopropylamine	17-23	monoamine oxidase B	Homo sapiens	80-85