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Request The Product List ofGlucose Transporter (GLUT) Glucose Transporter (GLUT)

Cat. No. Product Name Information
PC-25531

GLUT8 inhibitor P20

GLUT8 inhibitor

GLUT8 inhibitor P20 is a selective inhibitor of glucose transporter GLUT8 (SLC2A8) with IC50 of 2.1 uM,  2.9-fold selective over GLUT2.
PC-49286

SW157765

GLUT8 inhibitor

SW157765 (SW-157765) is a potent, specific inhibitor of glucose transporter GLUT8 (SLC2A8) with Kd of 200 nM, shows sensitivity to KRAS/KEAP1 double mutant NSCLC cells.
PC-47016

Glutipyran

GLUT inhibitor

Glutipyran is a small-molecule glucose transporter inhibitor, inhibits glycolytic activity and cell growth in human pancreatic cancer cells.
PC-73034

Glutor

GLUT inhibitor

Glutor (Glucose uptake inhibitor Glutor) is a novel highly potent glucose uptake inhibitor (IC50=10.8 nM) that selectively targets glucose transporters GLUT-1, -2, and -3.
PC-72556

KL-11743

GLUT inhibitor

KL-11743 (KL11743) is a potent, selective, orally bioavailable inhibitor of class I glucose transporters with IC50 of 115/137/90/68 nM for GLUT1/2/3/4, respectively.
PC-72387

DRB18

pan-GLUT inhibitor

DRB18 (DRB-18) is a potent, pan-class I glucose transporter (GLUT) inhibitor, reduces glucose uptake in HEK293 cell lines expressd single GLUT1-4 with IC50 of 0.9-8.8 uM.
PC-35327

WZB117

GLUT1 inhibitor

WZB117 (WZB-117) is a small-molecule inhibitor of glucose transporter 1 (GLUT1, SLC2A1), inhibits glucose transport and cancer cell proliferation with IC50 of 10 uM.
PC-62895

Fasentin

GLUT4 inhibitor

Fasentin is a novel inhibitor of glucose uptake (GLUT) that sensitizes cancer cells to FAS-induced cell death, preferentially inhibits GLUT4 (IC50=68 uM) over GLUT1.
PC-60884

GLUT4-IN-17

GLUT4 inhibitor

GLUT4-IN-17 is a potent, selective glucose transporter 4 (GLUT4) inhibitor with IC450 of 10.8 uM, inhibits MM cell proliferation.
PC-45543

STF-31

GLUT1 inhibitor

STF-31 is a selective GLUT1 inhibitor with IC50 of 1 uM, does not bind to other glucose transporters.
PC-42031

BAY-876

GLUT1 inhibitor

BAY-876 (BAY876) is a potent, highly selective and oral bioavailable GLUT1 inhibitor with IC50 of 2 nM.
PC-25569

MSNBA

GLUT5 inhibitor

MSNBA is a specific inhibitor of glucose transporter GLUT5, competitively inhibits GLUT5 fructose uptake with Ki of 3.2 uM, inhibits GLUT5 fructose transport in proteoliposomes with IC50 of 0.1 uM.

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