PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20002521-1	2010	The anti-parkinsonian drug, rasagiline [N-propargyl-1-(R)-aminoindan; Azilect(R)], is a secondary cyclic benzylamine and indane derivative, which provides irreversible, potent monoamine oxidase-B (MAO-B) inhibition and possesses neuroprotective and neurorestorative activities.	indan	121-127	monoamine oxidase B	Homo sapiens	176-195	
20002521-1	2010	The anti-parkinsonian drug, rasagiline [N-propargyl-1-(R)-aminoindan; Azilect(R)], is a secondary cyclic benzylamine and indane derivative, which provides irreversible, potent monoamine oxidase-B (MAO-B) inhibition and possesses neuroprotective and neurorestorative activities.	indan	121-127	monoamine oxidase B	Homo sapiens	197-202	
25820651-2	2015	Based on the structural similarity between alpha-tetralone and 1-indanone, the present study involved synthesis of 34 1-indanone and related indane derivatives as potential inhibitors of recombinant human MAO-A and MAO-B.	indan	141-147	monoamine oxidase B	Homo sapiens	215-220	
34047146-0	2021	New indane derivatives containing 2-hydrazinothiazole as potential acetylcholinesterase and monoamine oxidase-B inhibitors.	indan	4-10	monoamine oxidase B	Homo sapiens	92-111	
34047146-3	2021	In this study, indane ring which are in the structure of anticholinesterase effective molecules and 2-hydrazinothiazole structure whose inhibitory activities reported on monoamine oxidase-B (MAO-B) were combined; 4-(substituted phenyl)-2-[2-(3-phenyl-2,3-dihydro-1H-inden-1-ylidene) hydrazinyl]thiazole derivatives (3a-3i) were synthesized as dual inhibitors.	indan	15-21	monoamine oxidase B	Homo sapiens	170-189	
34047146-3	2021	In this study, indane ring which are in the structure of anticholinesterase effective molecules and 2-hydrazinothiazole structure whose inhibitory activities reported on monoamine oxidase-B (MAO-B) were combined; 4-(substituted phenyl)-2-[2-(3-phenyl-2,3-dihydro-1H-inden-1-ylidene) hydrazinyl]thiazole derivatives (3a-3i) were synthesized as dual inhibitors.	indan	15-21	monoamine oxidase B	Homo sapiens	191-196	
25820651-4	2015	C5-Substituted indanone and indane derivatives are comparatively weaker MAO-B inhibitors.	indan	28-34	monoamine oxidase B	Homo sapiens	72-77	
25820651-5	2015	Although the 1-indanone and indane derivatives are selective inhibitors of the MAO-B isoform, a number of homologues are also potent MAO-A inhibitors, with three homologues possessing IC50 values <0.1 muM.	indan	28-34	monoamine oxidase B	Homo sapiens	79-84