PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 31866563-3 2020 In this study, we hypothesized that NCS-382 is a substrate for the monocarboxylate transporter subtype 1 (MCT1) which is known to mediate blood-brain barrier (BBB) permeation of GHB. 4-hydroxybutyric acid 178-181 solute carrier family 16 member 1 Homo sapiens 67-104 33963018-13 2021 The results indicate that ethanol co-administered with GHB increases toxicity and MCT1 inhibition is effective in reversing toxicity by inhibiting GHB brain uptake when given post-GHB/ethanol administration. 4-hydroxybutyric acid 147-150 solute carrier family 16 member 1 Homo sapiens 82-86 33963018-13 2021 The results indicate that ethanol co-administered with GHB increases toxicity and MCT1 inhibition is effective in reversing toxicity by inhibiting GHB brain uptake when given post-GHB/ethanol administration. 4-hydroxybutyric acid 147-150 solute carrier family 16 member 1 Homo sapiens 82-86 33963018-15 2021 The effects of the novel MCT1 inhibitors AR-C155858 and AZD-3965 on this drug-drug interaction have not been studied before, and our preclinical studies indicate that MCT1 inhibitors can decrease brain concentrations of GHB by inhibiting brain uptake, even when administered at times after GHB/ethanol. 4-hydroxybutyric acid 220-223 solute carrier family 16 member 1 Homo sapiens 25-29 33963018-15 2021 The effects of the novel MCT1 inhibitors AR-C155858 and AZD-3965 on this drug-drug interaction have not been studied before, and our preclinical studies indicate that MCT1 inhibitors can decrease brain concentrations of GHB by inhibiting brain uptake, even when administered at times after GHB/ethanol. 4-hydroxybutyric acid 220-223 solute carrier family 16 member 1 Homo sapiens 167-171 33963018-15 2021 The effects of the novel MCT1 inhibitors AR-C155858 and AZD-3965 on this drug-drug interaction have not been studied before, and our preclinical studies indicate that MCT1 inhibitors can decrease brain concentrations of GHB by inhibiting brain uptake, even when administered at times after GHB/ethanol. 4-hydroxybutyric acid 290-293 solute carrier family 16 member 1 Homo sapiens 25-29 33963018-15 2021 The effects of the novel MCT1 inhibitors AR-C155858 and AZD-3965 on this drug-drug interaction have not been studied before, and our preclinical studies indicate that MCT1 inhibitors can decrease brain concentrations of GHB by inhibiting brain uptake, even when administered at times after GHB/ethanol. 4-hydroxybutyric acid 290-293 solute carrier family 16 member 1 Homo sapiens 167-171 31866563-3 2020 In this study, we hypothesized that NCS-382 is a substrate for the monocarboxylate transporter subtype 1 (MCT1) which is known to mediate blood-brain barrier (BBB) permeation of GHB. 4-hydroxybutyric acid 178-181 solute carrier family 16 member 1 Homo sapiens 106-110 17502341-1 2007 Monocarboxylate transporter 1 (MCT1) is an important determinant of the renal transport of the drug of abuse, gamma-hydroxybutyric acid (GHB). 4-hydroxybutyric acid 110-135 solute carrier family 16 member 1 Homo sapiens 0-29 17502341-1 2007 Monocarboxylate transporter 1 (MCT1) is an important determinant of the renal transport of the drug of abuse, gamma-hydroxybutyric acid (GHB). 4-hydroxybutyric acid 110-135 solute carrier family 16 member 1 Homo sapiens 31-35 17502341-1 2007 Monocarboxylate transporter 1 (MCT1) is an important determinant of the renal transport of the drug of abuse, gamma-hydroxybutyric acid (GHB). 4-hydroxybutyric acid 137-140 solute carrier family 16 member 1 Homo sapiens 0-29 17502341-1 2007 Monocarboxylate transporter 1 (MCT1) is an important determinant of the renal transport of the drug of abuse, gamma-hydroxybutyric acid (GHB). 4-hydroxybutyric acid 137-140 solute carrier family 16 member 1 Homo sapiens 31-35