PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2992386-1	1985	The QH2:cytochrome c oxidoreductase activity of the isolated bovine heart cytochrome b-c1 complex resolved into monomeric and dimeric form was titrated with three different inhibitors of electron transfer, antimycin, myxothiazol, and 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT).	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	234-278	LOC104968582	Bos taurus	8-20
10713075-6	2000	In the 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT)-inhibited complex, the rate of cytochrome c(1) reduction is greatly decreased to a t1/2 of approximately 2.8 s. An even lower rate is observed with the stigmatellin-treated complex.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	7-51	LOC104968582	Bos taurus	91-103
10713075-6	2000	In the 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT)-inhibited complex, the rate of cytochrome c(1) reduction is greatly decreased to a t1/2 of approximately 2.8 s. An even lower rate is observed with the stigmatellin-treated complex.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	53-58	LOC104968582	Bos taurus	91-103
10625445-4	1999	The displacement from an interface with cytochrome c(1) in native crystals to an interface with cytochrome b is induced by stigmatellin or 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT) and involves ligand formation between His-161 of the [2Fe-2S] binding cluster and the inhibitor.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	139-183	cytochrome c, somatic	Gallus gallus	40-52
10625445-4	1999	The displacement from an interface with cytochrome c(1) in native crystals to an interface with cytochrome b is induced by stigmatellin or 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT) and involves ligand formation between His-161 of the [2Fe-2S] binding cluster and the inhibitor.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	139-183	CYTB	Gallus gallus	96-108
10625445-4	1999	The displacement from an interface with cytochrome c(1) in native crystals to an interface with cytochrome b is induced by stigmatellin or 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT) and involves ligand formation between His-161 of the [2Fe-2S] binding cluster and the inhibitor.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	185-190	cytochrome c, somatic	Gallus gallus	40-52
10625445-4	1999	The displacement from an interface with cytochrome c(1) in native crystals to an interface with cytochrome b is induced by stigmatellin or 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT) and involves ligand formation between His-161 of the [2Fe-2S] binding cluster and the inhibitor.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	185-190	CYTB	Gallus gallus	96-108
2992386-1	1985	The QH2:cytochrome c oxidoreductase activity of the isolated bovine heart cytochrome b-c1 complex resolved into monomeric and dimeric form was titrated with three different inhibitors of electron transfer, antimycin, myxothiazol, and 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT).	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	280-285	LOC104968582	Bos taurus	8-20
2989259-3	1985	Cytochrome c reduction as catalyzed by Complex III displayed a residual, inhibitor-insensitive rate of 5% of the uninhibited rate for each of the three inhibitors, antimycin, myxothiazol, and UHDBT.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	192-197	LOC104968582	Bos taurus	0-12
6282879-1	1982	A synthetic quinone, 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT), inhibits electron transfer reactions in the cytochrome b-c1 segment of the mitochondrial respiratory chain.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	21-65	mitochondrially encoded cytochrome b	Homo sapiens	119-131
6282879-1	1982	A synthetic quinone, 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT), inhibits electron transfer reactions in the cytochrome b-c1 segment of the mitochondrial respiratory chain.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	67-72	mitochondrially encoded cytochrome b	Homo sapiens	119-131
6282879-3	1982	Thus, UHDBT inhibits reduction of cytochrome c1 by succinate and, if antimycin is added before succinate, UHDBT inhibits reduction of cytochrome b in addition to c1.	5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole	106-111	mitochondrially encoded cytochrome b	Homo sapiens	134-146