PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32496054-12	2020	Cinnamaldehyde and benzaldehyde were found to be the most potent inhibitors of microsomal CYP2A6 of the flavoring agents tested, with identified IC50 values of 1.1 muM and 3.0 muM, respectively.	benzaldehyde	19-31	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	90-96	
12746108-0	2003	More potent inhibition of human CYP2A6 than mouse CYP2A5 enzyme activities by derivatives of phenylethylamine and benzaldehyde.	benzaldehyde	114-126	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	32-38	
12746108-9	2003	Amphetamine is a weak inhibitor of CYP2A6, whereas benzaldehyde is a suicide inhibitor with K(inact) = 0.16 min(-1) and K(I) = 18 micro M. The K(ic) values of 2-phenylethylamine, 2-(p-tolyl)-ethylamine, 4-methylbenzaldehyde and 4-methoxybenzaldehyde were 1.13, 0.23, 0.36 and 0.73 micro M for CYP2A6, respectively.	benzaldehyde	51-63	cytochrome P450 family 2 subfamily A member 6	Homo sapiens	293-299