PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
1898024-5	1991	With either enantiomer of triphenylene 1,2-dihydrodiol, both purified cytochrome P450c (P450IA1) and liver microsomes from MC-treated rats formed diol epoxides and phenolic dihydrodiols in approximately equal amounts.	trans-1,2-dihydro-1,2-naphthalenediol	173-185	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	70-86	
21781864-5	1998	Stereoselective activation of B[c]Ph, the (+-)-B[c]Ph-3,4-dihydrodiol and its (-)-3R,4R-enantiomer to the fjord-region (-)-anti-B[c]PhDE occurred upon incubation with rat CYP1A1 and rat CYP1A2 as indicated by the formation of two stereoisomeric tetraols, the hydrolysis products of the labile anti-B[c]PhDE.	trans-1,2-dihydro-1,2-naphthalenediol	58-69	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	171-177	
10528997-2	1999	The dihydrodiol is metabolized at a rate of 2.4 nmol/nmol of cytochrome P450 1A1/min with microsomes from 3-methylcholanthrene-treated rats, a rate more than 10-fold higher than that observed with microsomes from control or phenobarbital-treated rats.	trans-1,2-dihydro-1,2-naphthalenediol	4-15	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	61-80	
3564534-6	1987	The 9,10-dihydro-9,10-dihydroxybenzo[a]pyrene was the major dihydrodiol formed by pulmonary cytochrome P-450MC.	trans-1,2-dihydro-1,2-naphthalenediol	60-71	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	103-110	
3564534-8	1987	Similar results concerning the related production of phenols and dihydrodiols, in the absence and presence of epoxide hydrolase, were obtained in reconstituted systems of hepatic cytochrome P-450MC, the major form of hepatic cytochrome P-450 from 3-methylcholanthrene-treated rats.	trans-1,2-dihydro-1,2-naphthalenediol	65-77	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	190-197	
6309378-6	1983	Benzo(a)pyrene was metabolized by AHH to dihydrodiols, quinones, and phenols in quantities which were about 10 times greater than those reported for rat lung microsomes.	trans-1,2-dihydro-1,2-naphthalenediol	41-53	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	34-37	
6865920-11	1983	The basis for this ratio in the latter case was explained by examination of the products formed from the (+)-(1S,2S)-and (-)-(1R,2R)-enantiomers of the dihydrodiol on metabolism by a highly purified system reconstituted with cytochrome P-450c.	trans-1,2-dihydro-1,2-naphthalenediol	152-163	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	225-242	
19330882-9	2009	The cytotoxicity of the dihydrodiol intermediates of B[a]P or DB[a,l]P was much greater, and similar in cell lines expressing either human or rat CYP1A1.	trans-1,2-dihydro-1,2-naphthalenediol	24-35	cytochrome P450, family 1, subfamily a, polypeptide 1	Rattus norvegicus	146-152