PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18623213-2	2009	Previous work has shown that amphiphilic diblock copolymers composed of methoxypolyethylene glycol-block-polycaprolactone (MePEG-b-PCL) diblock copolymers enhanced the cellular accumulation of Pgp substrates by modulating the function of this drug efflux transporter.	diblock copolymers	41-59	ATP binding cassette subfamily B member 1	Homo sapiens	193-196	
18623213-2	2009	Previous work has shown that amphiphilic diblock copolymers composed of methoxypolyethylene glycol-block-polycaprolactone (MePEG-b-PCL) diblock copolymers enhanced the cellular accumulation of Pgp substrates by modulating the function of this drug efflux transporter.	diblock copolymers	136-154	ATP binding cassette subfamily B member 1	Homo sapiens	193-196	
18623213-3	2009	The objective of this work was to determine whether MePEG-b-PCL diblock copolymers modulated Pgp function in multidrug resistant (MDR) cancer cells.	diblock copolymers	64-82	ATP binding cassette subfamily B member 1	Homo sapiens	93-96	
18380467-0	2008	P-glycoprotein efflux inhibition by amphiphilic diblock copolymers: relationship between copolymer concentration and substrate hydrophobicity.	diblock copolymers	48-66	ATP binding cassette subfamily B member 1	Homo sapiens	0-14	
18380467-3	2008	Therefore, the objectives of these studies were to assess if association of P-gp substrates differing in hydrophobicity will impact the effective concentration range for P-gp inhibition by amphiphilic diblock copolymers based on methoxypolyethylene glycol-block-polycaprolatone (MePEG-b-PCL).	diblock copolymers	201-219	ATP binding cassette subfamily B member 1	Homo sapiens	76-80	
18380467-3	2008	Therefore, the objectives of these studies were to assess if association of P-gp substrates differing in hydrophobicity will impact the effective concentration range for P-gp inhibition by amphiphilic diblock copolymers based on methoxypolyethylene glycol-block-polycaprolatone (MePEG-b-PCL).	diblock copolymers	201-219	ATP binding cassette subfamily B member 1	Homo sapiens	170-174	
12445560-1	2002	A series of diblock copolymers based on methoxypolyethylene glycol-block-poly(caprolactone) (MePEG-b-PCL) was synthesized and evaluated for enhancing the cellular accumulation of a P-glycoprotein (P-gp) substrate, rhodamine-123 (R-123), into caco-2 cells.	diblock copolymers	12-30	ATP binding cassette subfamily B member 1	Homo sapiens	181-195	
12445560-1	2002	A series of diblock copolymers based on methoxypolyethylene glycol-block-poly(caprolactone) (MePEG-b-PCL) was synthesized and evaluated for enhancing the cellular accumulation of a P-glycoprotein (P-gp) substrate, rhodamine-123 (R-123), into caco-2 cells.	diblock copolymers	12-30	ATP binding cassette subfamily B member 1	Homo sapiens	197-201