PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
8476845-5	1993	The benzo[a]pyrene ring of [BP]dG6 is intercalated between intact Watson-Crick dC5.dG18 and dC7.dG16 base pairs in a right-handed DNA helix.	Benzo(a)pyrene	4-18	E(rst)C7	Drosophila melanogaster	92-95
15322362-2	2004	The stereogenic center at C-15 of 1 originated from that of the enantiomers of citronellal, and that at C-7 was generated by lipase-catalyzed asymmetric acetylation of (3RS,11R)- and (3RS,11S)-17-methyl-1-trimethylsilylpentacos-1-yn-3-ol (13).	,11r)	172-177	E(rst)C7	Drosophila melanogaster	104-107
15322362-2	2004	The stereogenic center at C-15 of 1 originated from that of the enantiomers of citronellal, and that at C-7 was generated by lipase-catalyzed asymmetric acetylation of (3RS,11R)- and (3RS,11S)-17-methyl-1-trimethylsilylpentacos-1-yn-3-ol (13).	,11s)-17-methyl-1-trimethylsilylpentacos-1-yn-3-ol	187-237	E(rst)C7	Drosophila melanogaster	104-107
10451381-6	1999	The aminopyrene ring of [AP]dG6 is intercalated into the DNA helix between intact Watson-Crick dC5.dG18 and dC7.dG16 base pairs and is in contact with dC5, dC7, dG16, dA17, and dG18 residues that form a hydrophobic pocket around it.	Aminopyrine	4-15	E(rst)C7	Drosophila melanogaster	108-111
10451381-6	1999	The aminopyrene ring of [AP]dG6 is intercalated into the DNA helix between intact Watson-Crick dC5.dG18 and dC7.dG16 base pairs and is in contact with dC5, dC7, dG16, dA17, and dG18 residues that form a hydrophobic pocket around it.	Aminopyrine	4-15	E(rst)C7	Drosophila melanogaster	156-159
10451381-1	1999	Solution structural studies have been undertaken on the aminopyrene-C(8)-dG ([AP]dG) adduct in the d(C5-[AP]G6-C7).	aminopyrene-c(8)-dg	56-75	E(rst)C7	Drosophila melanogaster	111-113
10451381-1	1999	Solution structural studies have been undertaken on the aminopyrene-C(8)-dG ([AP]dG) adduct in the d(C5-[AP]G6-C7).	[ap]dg	77-83	E(rst)C7	Drosophila melanogaster	111-113
8841109-1	1996	Combined NMR-molecular mechanics computational studies were undertaken on the C8-deoxyguanosine adduct formed by the carcinogen 1-nitropyrene embedded in the d(C5-[AP]G6-C7).d(G16-C17-G18) sequence context in a 11-mer duplex, with dC opposite the modified deoxyguanosine.	c8-deoxyguanosine	78-95	E(rst)C7	Drosophila melanogaster	170-172
8841109-1	1996	Combined NMR-molecular mechanics computational studies were undertaken on the C8-deoxyguanosine adduct formed by the carcinogen 1-nitropyrene embedded in the d(C5-[AP]G6-C7).d(G16-C17-G18) sequence context in a 11-mer duplex, with dC opposite the modified deoxyguanosine.	1-nitropyrene	128-141	E(rst)C7	Drosophila melanogaster	170-172
8841109-1	1996	Combined NMR-molecular mechanics computational studies were undertaken on the C8-deoxyguanosine adduct formed by the carcinogen 1-nitropyrene embedded in the d(C5-[AP]G6-C7).d(G16-C17-G18) sequence context in a 11-mer duplex, with dC opposite the modified deoxyguanosine.	Deoxyguanosine	81-95	E(rst)C7	Drosophila melanogaster	170-172
8841109-5	1996	The aminopyrene ring of [AP]dG6 is intercalated into the DNA helix between intact Watson-Crick dC5.dG18 and dC7.dG16 base pairs.	Aminopyrine	4-15	E(rst)C7	Drosophila melanogaster	108-111
8841109-5	1996	The aminopyrene ring of [AP]dG6 is intercalated into the DNA helix between intact Watson-Crick dC5.dG18 and dC7.dG16 base pairs.	[ap]dg6	24-31	E(rst)C7	Drosophila melanogaster	108-111