PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29758567-7	2018	The effect of the heteroaromatic substituent on MAO-B inhibition activity, in decreasing order was found to be: cyclohexyl, phenyl>thiophene>pyridine, furane, pyrrole, cyclopentyl.	furan	157-163	monoamine oxidase B	Homo sapiens	48-53	
23860591-3	2013	The results demonstrate that these furan substituted phenylpropenones exhibited moderate to good inhibitory activities towards MAO-B, but showed weak or no inhibition of the MAO-A enzyme.	furan	35-40	monoamine oxidase B	Homo sapiens	127-132	
25788143-2	2016	Herein described is pharmacophore generation and atom-based 3D-QSAR analysis of previously reported furan based MAO-B inhibitors in order to get insight into their structural requirements responsible for high affinity.	furan	100-105	monoamine oxidase B	Homo sapiens	112-117