PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23743277-1	2013	Benzimidazole and indane are the two key fragments in our potent and selective MCH-1 receptor (MCHR1) antagonists.	benzimidazole	0-13	melanin concentrating hormone receptor 1	Homo sapiens	95-100	
20724156-2	2010	The synthesis and biological evaluation of novel benzimidazole derivatives as MCHR1 antagonists are described.	benzimidazole	49-62	melanin concentrating hormone receptor 1	Homo sapiens	78-83	
16690315-2	2006	Novel benzimidazole analogues with increased chemical stability, devoid of the potential carcinogenic liability associated with a biarylamine moiety, were synthesized and evaluated to be potent MCH R1 antagonists.	benzimidazole	6-19	melanin concentrating hormone receptor 1	Homo sapiens	194-200	
17178222-0	2007	Quinazoline and benzimidazole MCH-1R antagonists.	benzimidazole	16-29	melanin concentrating hormone receptor 1	Homo sapiens	30-36	
16904318-0	2006	Novel benzimidazole-based MCH R1 antagonists.	benzimidazole	6-19	melanin concentrating hormone receptor 1	Homo sapiens	26-32	
16904318-1	2006	The identification of an MCH R1 antagonist screening hit led to the optimization of a class of benzimidazole-based MCH R1 antagonists.	benzimidazole	95-108	melanin concentrating hormone receptor 1	Homo sapiens	25-31	
16904318-1	2006	The identification of an MCH R1 antagonist screening hit led to the optimization of a class of benzimidazole-based MCH R1 antagonists.	benzimidazole	95-108	melanin concentrating hormone receptor 1	Homo sapiens	115-121