PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8496909-0	1993	Mechanism-based inhibitors of prostaglandin omega-hydroxylase: (R)- and (S)-12-hydroxy-16-heptadecynoic acid and 2,2-dimethyl-12-hydroxy-16-heptadecynoic acid.	12-hydroxy-16-heptadecynoic acid	72-108	cytochrome P450 4A5	Oryctolagus cuniculus	30-61	
8496909-1	1993	12-Hydroxy-16-heptadecynoic acid has been shown to selectively inactivate cytochrome P450 4A4, a pulmonary cytochrome P450 enzyme that catalyzes the omega-hydroxylation of prostaglandins [Muerhoff, A. S.; Williams, D. E.; Reich, N. O.; CaJacob, C. A.; Ortiz de Montellano, P. R.; Masters, B. S. S. J. Biol.	12-hydroxy-16-heptadecynoic acid	0-32	cytochrome P450 4A5	Oryctolagus cuniculus	74-93	
8496909-5	1993	In a continuing effort to develop such agents, the two enantiomers of 12-hydroxy-16-heptadecynoic acid have been stereospecifically synthesized, their absolute stereochemistry confirmed, and the dependence of enzyme inactivation on absolute stereochemistry determined using cytochrome P450 4A4 purified from the lungs of pregnant rabbits.	12-hydroxy-16-heptadecynoic acid	70-102	cytochrome P450 4A5	Oryctolagus cuniculus	274-293