PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21393174-11 2011 Growth inhibition assays suggest that elvitegravir, raltegravir and vicriviroc are substrates of ABCB1. Raltegravir Potassium 52-63 ATP binding cassette subfamily B member 1 Homo sapiens 97-102 27097364-0 2016 Brief Report: High Peak Level of Plasma Raltegravir Concentration in Patients With ABCB1 and ABCG2 Genetic Variants. Raltegravir Potassium 40-51 ATP binding cassette subfamily B member 1 Homo sapiens 83-88 27097364-1 2016 Raltegravir was recently identified to be a substrate of ATP-binding cassette transporter B1 (ABCB1) and G2 (ABCG2), which are efflux transporters and expressed in the intestines. Raltegravir Potassium 0-11 ATP binding cassette subfamily B member 1 Homo sapiens 57-92 27097364-1 2016 Raltegravir was recently identified to be a substrate of ATP-binding cassette transporter B1 (ABCB1) and G2 (ABCG2), which are efflux transporters and expressed in the intestines. Raltegravir Potassium 0-11 ATP binding cassette subfamily B member 1 Homo sapiens 94-99 27097364-2 2016 We analyzed the relations between plasma raltegravir concentrations and single nucleotide polymorphism of ABCB1 and ABCG2 genes. Raltegravir Potassium 41-52 ATP binding cassette subfamily B member 1 Homo sapiens 106-111 27097364-3 2016 The peak plasma concentration of raltegravir was significantly higher in the patients with ABCB1 4036 AG/GG and ABCG2 421 CA/AA than in other genotype holders (P = 0.0052), though no difference was identified in trough raltegravir concentrations, which may be explained by reduced expression of efflux transporters in intestine by these genetic variants. Raltegravir Potassium 33-44 ATP binding cassette subfamily B member 1 Homo sapiens 91-96 24872134-3 2014 In the present study, we analyzed the relationship between single-nucleotide polymorphisms of ABCB1 and ABCG2 genes and raltegravir concentrations in 31 plasma and 14 CSF samples of HIV-infected patients treated with raltegravir-containing regimens. Raltegravir Potassium 120-131 ATP binding cassette subfamily B member 1 Homo sapiens 94-99 24872134-3 2014 In the present study, we analyzed the relationship between single-nucleotide polymorphisms of ABCB1 and ABCG2 genes and raltegravir concentrations in 31 plasma and 14 CSF samples of HIV-infected patients treated with raltegravir-containing regimens. Raltegravir Potassium 217-228 ATP binding cassette subfamily B member 1 Homo sapiens 94-99 22450971-7 2012 Cellular accumulation studies were used to determine the effect of interplay between pH and ABCB1 transport on raltegravir accumulation. Raltegravir Potassium 111-122 ATP binding cassette subfamily B member 1 Homo sapiens 92-97 22450971-15 2012 Cellular accumulation of raltegravir was increased independently by inhibiting ABCB1 and by lowering extracellular pH from pH 8 to 5. Raltegravir Potassium 25-36 ATP binding cassette subfamily B member 1 Homo sapiens 79-84 23707228-0 2013 Determination of P-glycoprotein surface expression and functional ability after in vitro treatment with darunavir or raltegravir in lymphocytes of healthy donors. Raltegravir Potassium 117-128 ATP binding cassette subfamily B member 1 Homo sapiens 17-31 23707228-3 2013 Blood samples from 16 healthy volunteers were used to determine the expression of P-gp on total, T and T helper lymphocytes after exposure to darunavir, a second generation protease inhibitor, and raltegravir, the first approved integrase inhibitor. Raltegravir Potassium 197-208 ATP binding cassette subfamily B member 1 Homo sapiens 82-86 21078936-2 2011 Here we determined whether raltegravir was a substrate for ABCB1 or the influx transporters SLCO1A2, SLCO1B1, SLCO1B3, SLC22A1, SLC22A6, SLC10A1, SLC15A1, and SLC15A2. Raltegravir Potassium 27-38 ATP binding cassette subfamily B member 1 Homo sapiens 59-64 21078936-3 2011 Raltegravir transport by ABCB1 was studied with CEM, CEM(VBL100), and Caco-2 cells. Raltegravir Potassium 0-11 ATP binding cassette subfamily B member 1 Homo sapiens 25-30 21078936-6 2011 Raltegravir was confirmed to be an ABCB1 substrate in CEM, CEM(VBL100), and Caco-2 cells. Raltegravir Potassium 0-11 ATP binding cassette subfamily B member 1 Homo sapiens 35-40