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GPCR/G Protein
Glucose Transporter

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Glucose Transporter

Chemical Structure Cat. No. Product Name CAS No.
GLUT inhibitor-1 Chemical Structure
BCP46268 GLUT inhibitor-1 2421141-40-2
GLUT inhibitor-1 is a potent and orally active inhibitor of glucose transporters, targeting both GLUT1 and GLUT3 , with IC 50 s of 242 nM and 179 nM, respectively.
KL-11743 Chemical Structure
BCP45095 KL-11743 1369452-53-8
KL-11743 is a potent, bioavailable inhibitor of class I glucose transporters.
Fasentin Chemical Structure
BCP41879 Fasentin 392721-37-8
Fasentin is a GLUT1 and GLUT4 inhibitor (IC50 = 68 μM). Fasentin sensitizes Fas receptor in a range of tumor cell lines (IC50 = 20 μM) via regulating the extrinsic apoptotic pathway downstream of TNF receptors but upstream of effector caspases.
BAY-876 Chemical Structure
BCP25065 BAY-876 1799753-84-6
BAY-876 is the first highly selective GLUT1 inhibitor with IC50 of 0.002 uM.
STF-31 Chemical Structure
BCP16022 STF-31 724741-75-7
STE31 is a potent glucose transporter 1 (GLUT1). STF31 selectively kills RCCs by specifically targeting glucose uptake through GLUT1 and exploiting the unique dependence of these cells on GLUT1 for survival.
WZB117 Chemical Structure
BCP24665 WZB117 1223397-11-2
WZB117 is a potent Glut1 inhibitor.