Flavonoid with anti-oxidant, anti-cancer and anti-angiogenic activity that arrests the cell cycle at the G0/G1 phase.
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A cell-permeable, partly selective DUB inhibitor, directly inhibiting DUB activity of USP9x, USP5, USP14, and UCH37.
A cell-permeable, selective PPARα agonist with weaker binding to PPARγ and PPARδ.
Inhibitor of Glucose Transporter 1 (GLUT1) which also inhibits cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells.
A potent and selective endothelial lipase (EL) inhibitor.
An orally bioavailable, ATP-competitive, small-molecule inhibitor of heat shock protein 90 (Hsp90) with potential antineoplastic activity.
Z-AEVD-FMK is a synthetic peptide inhibitor that inhibits caspase-10 and related caspase activity.
A cell-permeable caspase-3 inhibitor.
Cell-permeable, irreversible inhibitor of cathepsins B, L, and S, and likely cathepsin H which is also a useful negative control for FMK-labeled caspase inhibitors.
Cell-permeable, selective inhibitor of cGMP-specific phosphodiesterase (PDE V).
A potent inhibitor of cytidine deaminase and DNA methylation that displays antitumor properties.
A potent and reversible 5-lipoxygenase (5-LOX) inhibitor that inhibits LTB4 synthesis.
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