PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15861398-3	2005	Recently, we observed the extreme sensitivity of PARP-1 knock-out (KO) cells to C-1305, a new biologically active triazoloacridone compound.	C 1305	80-86	poly (ADP-ribose) polymerase family, member 1	Mus musculus	49-55	
20067769-1	2010	Our previous studies have shown that murine fibroblast cells, in which PARP-1 gene was inactivated by gene disruption, are extremely sensitive to triazoloacridone compound C-1305, an inhibitor of DNA topoisomerase II with unusual properties.	C 1305	172-178	poly (ADP-ribose) polymerase family, member 1	Mus musculus	71-77	
15231658-4	2004	The IC(50) concentration of C-1305 determined for PARP-1 knockout cells was approximately 150-fold lower than that determined for cells with functional PARP-1.	C 1305	28-34	poly (ADP-ribose) polymerase family, member 1	Mus musculus	50-56	
15231658-4	2004	The IC(50) concentration of C-1305 determined for PARP-1 knockout cells was approximately 150-fold lower than that determined for cells with functional PARP-1.	C 1305	28-34	poly (ADP-ribose) polymerase family, member 1	Mus musculus	152-158	
15231658-7	2004	C-1305 strongly affected cell cycle progression in normal and PARP-1 mutant cells and arrested both cell types in G(2)-M phase.	C 1305	0-6	poly (ADP-ribose) polymerase family, member 1	Mus musculus	62-68	
15231658-9	2004	Together, these results show that mouse cells lacking PARP-1 are extremely sensitive to C-1305, a new topoisomerase II inhibitor.	C 1305	88-94	poly (ADP-ribose) polymerase family, member 1	Mus musculus	54-60