Fasentin

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Fasentin

CAS No. : 392721-37-8

Biological Activity:Fasentin, a potent glucose uptake inhibitor, inhibits GLUT-1/GLUT-4 transporters. Fasentin preferentially inhibits GLUT4 (IC50=68 μM) over GLUT1. Fasentin is a death receptor stimuli (FAS) sensitizer and sensitizes cells to FAS-induced cell death. Fasentin is also a tumor necrosis factor (TNF) apoptosis-inducing ligand sensitizer. Fasentin blocks glucose uptake in cancer cell lines and has anti-angiogenic activity[2][3].

Research Area:Cancer|Cardiovascular Disease

Targets:TNF Receptor|GLUT|Apoptosis

Related Screening Libraries:Bioactive Compound Library Plus;Apoptosis Compound Library;Immunology/Inflammation Compound Library;Membrane Transporter/Ion Channel Compound Library;Anti-Cancer Compound Library;Anti-Cardiovascular Disease Compound Library;Glycolysis Compound Library;Glutamine Metabolism Compound Library;Anti-Cancer Metabolism Compound Library;Angiogenesis-Related Compound Library;Glucose Metabolism Compound Library;Targeted Diversity Library;Human Metabolite Library;

Related Small Molecules:Physalin A;Bomedemstat ditosylate;Akt/NF-κB/JNK-IN-1;Enpp/Carbonic anhydrase-IN-1;GK563;Calpeptin;Lobetyolin;AX-024;BJE6-106;Dinaciclib;Ecteinascidin 770;MDM2-p53-IN-15;AT9283;Staurosporine;SNS-032;C188-9;ZLDI-8;Topoisomerase I/II inhibitor 3;Xevinapant;Mangiferin;Cambinol;Antioxidant agent-5;Apoptosis inducer 9;Bafetinib;Cyclovirobuxine D

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