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BAY-876

CAS No. : 1799753-84-6

Biological Activity：BAY-876 is an orally active and selective glucose transporter 1 (GLUT1) inhibitor with an IC₅₀ of 2 nM. BAY-876 is >130-fold more selective for GLUT1 than GLUT2, GLUT3, and GLUT4. BAY-876 is also a potent blocker of glycolytic metabolism and ovarian cancer growth^[2].

Research Area：Cancer

Targets：GLUT

Related Screening Libraries:Bioactive Compound Library Plus;Membrane Transporter/Ion Channel Compound Library;Anti-Cancer Compound Library;Glycolysis Compound Library;Orally Active Compound Library;Chemical Probe Library;Glutamine Metabolism Compound Library;Anti-Cancer Metabolism Compound Library;Glucose Metabolism Compound Library;Targeted Diversity Library;

Related Small Molecules:Sennidin A;Licarin B;GLUT4 activator 1;GLUT4-IN-2;STF-31;KPH2f;MOTS-c(human) acetate;Phloretin;GLUT inhibitor-1;4,6-O-Ethylidene-α-D-glucose;WZB117;GLUT1-IN-1;SW157765;Lavendustin B;Avicularin;Rhoifolin;Fasentin;KL-11743;GLUT1-IN-2;DRB18

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