PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19919114-4	2009	Urolithin A, a microbial metabolite, was the most potent uncompetitive inhibitor of CYP1B1-mediated EROD activity, exhibiting 2-fold selectivity over CYP1A1, while urolithin B was a noncompetitive inhibitor with 3-fold selectivity.	3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one	0-11	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	150-156	
19919114-7	2009	Urolithins A and B showed a decrease in their CYP1-mediated EROD inhibitory IC50 values upon increasing their treatment times from 30 min to 24 h. Urolithin C, 8-O-methylurolithin A, and 8,9-di-O-methylurolithin C caused a potent CYP1-mediated EROD inhibition in 22Rv1 cells upon 24 h of incubation.	3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one	0-12	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	46-50	
19919114-7	2009	Urolithins A and B showed a decrease in their CYP1-mediated EROD inhibitory IC50 values upon increasing their treatment times from 30 min to 24 h. Urolithin C, 8-O-methylurolithin A, and 8,9-di-O-methylurolithin C caused a potent CYP1-mediated EROD inhibition in 22Rv1 cells upon 24 h of incubation.	3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one	0-12	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	230-234