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Home >> Signaling Pathways >> Membrane Transporter/Ion Channel >> Glucose Transporters

Glucose Transporters

Products for  Glucose Transporters

  1. Cat.No. Product Name Information
  2. GC64568 DRB18 DRB18 is a potent pan-class GLUT inhibitor. DRB18 alters energy-related metabolism in A549 cells by changing the abundance of metabolites in glucose-related pathways. DRB18 can eventually lead to G1/S phase arrest and increase oxidative stress and necrotic cell death. DRB18 has anti-tumor activity. DRB18 Chemical Structure
  3. GC43654 Fasentin Fasentin is an inhibitor of glucose transport. Fasentin Chemical Structure
  4. GC64876 GLUT inhibitor-1 GLUT inhibitor-1 is a potent and orally active inhibitor of glucose transporters, targeting both GLUT1 and GLUT3, with IC50s of 242 nM and 179 nM, respectively. GLUT inhibitor-1 Chemical Structure
  5. GC73808 Glutor Glutor is a selective GLUT 1/2/3 inhibitor that can suppress glucose uptake. Glutor Chemical Structure
  6. GC64014 KL-11743 KL-11743 is a potent, orally active, and glucose-competitive inhibitor of the class I glucose transporters, with IC50s of 115, 137, 90, and 68 nM for GLUT1, GLUT2, GLUT3, and GLUT4, respectively. KL-11743 Chemical Structure
  7. GC70894 KPH2f KPH2f is a safe, orally active, and effective dual URAT1/GLUT9 inhibitor with IC50s of 0.24 μM and 9.37 μM for URAT1 and GLUT9, respectively. KPH2f Chemical Structure
  8. GC45494 Lavendustin B   Lavendustin B Chemical Structure
  9. GC69481 MMV009085

    MMV009085 is an effective inhibitor of the Plasmodium falciparum hexose transporter PfHT1, making it a potential anti-malaria compound. It also inhibits human glucose transporters, with strong inhibitory effects on glucose uptake (IC50: 2.6 μM) and parasite growth (EC50: 1.23±0.04 μM; 3D7).

     MMV009085 Chemical Structure
  10. GC72650 MSNBA MSNBA is a specific inhibitor of GLUT5 fructose transport in proteoliposomes. MSNBA Chemical Structure
  11. GC71079 SLC26A3-IN-2 SLC26A3-IN-2 is an orally active inhibitor of anion exchanger protein SLC26A3 (IC50=360 nM). SLC26A3-IN-2 Chemical Structure
  12. GC14803 STF 31 GLUT1 and NAMPT inhibitor STF 31 Chemical Structure
  13. GC66470 SW157765 SW157765 is a selective non-canonical glucose transporter GLUT8 (SLC2A8) inhibitor. KRAS/KEAP1 double mutant NSCLC cells are selectively sensitive to the SW157765, due to the convergent consequences of dual KRAS and NRF2 modulation of metabolic and xenobiotic gene regulatory programs. SW157765 Chemical Structure
  14. GC13381 WZB117

    Glucose Transporter Inhibitor IV

     Glucose transporter 1 (Glut1) inhibitor WZB117 Chemical Structure

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