PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19888760-0 2009 Synthesis and evaluation of a new generation of orally efficacious benzimidazole-based poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors as anticancer agents. benzimidazole 67-80 poly (ADP-ribose) polymerase family, member 1 Mus musculus 87-116 19888760-0 2009 Synthesis and evaluation of a new generation of orally efficacious benzimidazole-based poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors as anticancer agents. benzimidazole 67-80 poly (ADP-ribose) polymerase family, member 1 Mus musculus 118-124 19888760-2 2009 As one of the strategies to expand our portfolio of PARP-1 inhibitors, we pursued unsaturated heterocycles to replace the saturated cyclic amine derivatives appended to the benzimidazole core. benzimidazole 173-186 poly (ADP-ribose) polymerase family, member 1 Mus musculus 52-58 18541433-1 2008 We have developed a series of cyclic amine-containing benzimidazole carboxamide poly(ADP-ribose)polymerase (PARP) inhibitors, with good PARP-1 enzyme potency, as well as cellular potency. benzimidazole 54-67 poly (ADP-ribose) polymerase family, member 1 Mus musculus 80-106 18541433-1 2008 We have developed a series of cyclic amine-containing benzimidazole carboxamide poly(ADP-ribose)polymerase (PARP) inhibitors, with good PARP-1 enzyme potency, as well as cellular potency. benzimidazole 54-67 poly (ADP-ribose) polymerase family, member 1 Mus musculus 108-112 18541433-1 2008 We have developed a series of cyclic amine-containing benzimidazole carboxamide poly(ADP-ribose)polymerase (PARP) inhibitors, with good PARP-1 enzyme potency, as well as cellular potency. benzimidazole 54-67 poly (ADP-ribose) polymerase family, member 1 Mus musculus 136-142 18586490-0 2008 Synthesis and SAR of novel, potent and orally bioavailable benzimidazole inhibitors of poly(ADP-ribose) polymerase (PARP) with a quaternary methylene-amino substituent. benzimidazole 59-72 poly (ADP-ribose) polymerase family, member 1 Mus musculus 87-114 18586490-0 2008 Synthesis and SAR of novel, potent and orally bioavailable benzimidazole inhibitors of poly(ADP-ribose) polymerase (PARP) with a quaternary methylene-amino substituent. benzimidazole 59-72 poly (ADP-ribose) polymerase family, member 1 Mus musculus 116-120 18586490-3 2008 Utilizing a benzimidazole carboxamide scaffold in which the amide forms a key intramolecular hydrogen bond for optimal interaction with the enzyme, we have identified a novel series of PARP inhibitors containing a quaternary methylene-amino substituent at the C-2 position of the benzimidazole. benzimidazole 12-25 poly (ADP-ribose) polymerase family, member 1 Mus musculus 185-189