PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
14747463-7	2004	Consistent with a late endocytic protein trafficking defect, the hydrophobic amine U18666A retained NPC1 in abnormally tubulated, cholesterol-poor, Tangier disease late endosomes, rather than cholesterol-laden lysosomes, as in wild type fibroblasts.	Amines	77-82	NPC intracellular cholesterol transporter 1	Homo sapiens	100-104	
18591242-0	2008	Niemann-Pick C1 functions in regulating lysosomal amine content.	Amines	50-55	NPC intracellular cholesterol transporter 1	Homo sapiens	0-15	
18591242-3	2008	We show here that the introduction of amine-containing molecules in lysosomes can significantly stimulate NPC1-mediated late endosome/lysosome fusion, and subsequently the secretion of lysosomal cargo.	Amines	38-43	NPC intracellular cholesterol transporter 1	Homo sapiens	106-110	
10666334-7	2000	Incubation of granulosa-lutein cells with low-density lipoprotein (LDL) in the presence of the hydrophobic amine, U18666A, caused accumulation of free cholesterol in granules, identified by filipin staining, that contained LAMP-2 and NPC1.	Amines	107-112	NPC intracellular cholesterol transporter 1	Homo sapiens	234-238