GLUT

亜型選択性的な製品

GLUT製品

  • All (8)
  • GLUT阻害剤 (6)
  • 新製品
製品コード 製品名称 製品説明 文献中Selleckの製品使用例 お客様のフィードバック
S8452 BAY-876 BAY-876 is a potent and selective GLUT1 inhibitor (IC50=0.002 μM) with a selectivity factor of >100 against GLUT2, GLUT3, and GLUT4.
Am J Pathol, 2024, S0002-9440(24)00116-0
Cancer Cell Int, 2024, 24(1):19
Sci Rep, 2024, 14(1):15340
S7931 STF-31 STF-31 is a selective glucose transporter GLUT1 inhibitor.
Immunity, 2022, 55(1):159-173.e9
J Control Release, 2022, 352:540-555
Mol Oncol, 2022, 16(15):2861-2880
S7927 WZB117 WZB117 is an inhibitor of Glucose Transporter 1 (GLUT1). It inhibited cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells with an IC50 of approximately 10 μM.
Nat Commun, 2024, 15(1):4363
Am J Pathol, 2024, S0002-9440(24)00116-0
Sci Rep, 2024, 14(1):15340
F3128New GLUT4 mAb
E0805 KL-11743 KL-11743 is a potent glucose-competitive inhibitor of the class I glucose transporters with IC50s of 115, 137 and 90 nM for GLUT1, GLUT2, and GLUT3.
Sci Rep, 2024, 14(1):15340
S5748 4′-Deoxyphlorizin 4'-Deoxyphlorizin is an inhibitor of the glucose transport system.
F1192New Glucose Transporter GLUT1 Rabbit mAb Glucose Transporter GLUT1 Rabbit mAb detects endogenous levels of total Glucose Transporter GLUT1 protein.
S0235 Lavendustin B Lavendustin B inhibits HIV-1 integrase (IN) interaction with its cognate cellular cofactor lens epithelium-derived growth factor (LEDGF/p75). Lavendustin B is an inhibitor of Tyrosine Kinase and also a competitive inhibitor of glucose transporter 1 (Glut1).
S8452 BAY-876 BAY-876 is a potent and selective GLUT1 inhibitor (IC50=0.002 μM) with a selectivity factor of >100 against GLUT2, GLUT3, and GLUT4.
Am J Pathol, 2024, S0002-9440(24)00116-0
Cancer Cell Int, 2024, 24(1):19
Sci Rep, 2024, 14(1):15340
S7931 STF-31 STF-31 is a selective glucose transporter GLUT1 inhibitor.
Immunity, 2022, 55(1):159-173.e9
J Control Release, 2022, 352:540-555
Mol Oncol, 2022, 16(15):2861-2880
S7927 WZB117 WZB117 is an inhibitor of Glucose Transporter 1 (GLUT1). It inhibited cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells with an IC50 of approximately 10 μM.
Nat Commun, 2024, 15(1):4363
Am J Pathol, 2024, S0002-9440(24)00116-0
Sci Rep, 2024, 14(1):15340
E0805 KL-11743 KL-11743 is a potent glucose-competitive inhibitor of the class I glucose transporters with IC50s of 115, 137 and 90 nM for GLUT1, GLUT2, and GLUT3.
Sci Rep, 2024, 14(1):15340
S5748 4′-Deoxyphlorizin 4'-Deoxyphlorizin is an inhibitor of the glucose transport system.
S0235 Lavendustin B Lavendustin B inhibits HIV-1 integrase (IN) interaction with its cognate cellular cofactor lens epithelium-derived growth factor (LEDGF/p75). Lavendustin B is an inhibitor of Tyrosine Kinase and also a competitive inhibitor of glucose transporter 1 (Glut1).
F3128New GLUT4 mAb
F1192New Glucose Transporter GLUT1 Rabbit mAb Glucose Transporter GLUT1 Rabbit mAb detects endogenous levels of total Glucose Transporter GLUT1 protein.

GLUT阻害剤の選択性比較

Tags: GLUT inhibitor|GLUT agonist|GLUT activator|GLUT inducer|GLUT antagonist|GLUT signaling pathway|GLUT assay kit