PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
15935825-5	2005	We studied the reaction of isomers of benzene diolepoxide, namely syn-((+/-)BDE1) and anti-BDE ((+/-)BDE2), with sulfhydryl groups in vitro.	benzene diolepoxide	38-57	HLCS intronic transcript 1	Homo sapiens	76-80
17177461-4	2006	It appears that commonly cited bond energies for cyclopropane, cyclobutane, and cyclohexane are 3 to 4 kcal mol-1 too small and their pi bond strengths, as given by BDE1 - BDE2, are in error by up to 8 kcal mol-1.	cyclopropane	49-61	HLCS intronic transcript 1	Homo sapiens	165-169
17177461-4	2006	It appears that commonly cited bond energies for cyclopropane, cyclobutane, and cyclohexane are 3 to 4 kcal mol-1 too small and their pi bond strengths, as given by BDE1 - BDE2, are in error by up to 8 kcal mol-1.	Cyclobutanes	63-74	HLCS intronic transcript 1	Homo sapiens	165-169
17177461-4	2006	It appears that commonly cited bond energies for cyclopropane, cyclobutane, and cyclohexane are 3 to 4 kcal mol-1 too small and their pi bond strengths, as given by BDE1 - BDE2, are in error by up to 8 kcal mol-1.	Cyclohexane	80-91	HLCS intronic transcript 1	Homo sapiens	165-169
15839713-9	2005	Additivity was found to work well for m-benzoquinone, but BDE1 and BDE2 for 1,2- and 1,4-dihydroxybenzene differed by a remarkably small 14.1 +/- 4.2 and 23.5 +/- 3.7 kcal mol(-)(1), respectively, indicating that o- and p-benzoquinone should be excellent radical traps.	1,2- and 1,4-dihydroxybenzene	76-105	HLCS intronic transcript 1	Homo sapiens	58-62
15839713-9	2005	Additivity was found to work well for m-benzoquinone, but BDE1 and BDE2 for 1,2- and 1,4-dihydroxybenzene differed by a remarkably small 14.1 +/- 4.2 and 23.5 +/- 3.7 kcal mol(-)(1), respectively, indicating that o- and p-benzoquinone should be excellent radical traps.	o- and p-benzoquinone	213-234	HLCS intronic transcript 1	Homo sapiens	58-62