Birinapant, also known as TL32711, is a synthetic small molecule and peptido mimetic of second mitochondrial-derived activator of caspases (SMAC) and inhibitor of IAP (Inhibitor of Apoptosis Protein) family proteins, with potential antineoplastic activity.
More Information Supplier PageIWR-1-endo is a potent inhibitor of the Wnt response, blocking a cell-based Wnt/??-catenin pathway reporter response with an IC50 value of 180 nM. Wnt proteins bind to receptors on the cell surface, initiating a signaling cascade that leads to ??-catenin activation of gene transcription.
More Information Supplier PageIWR-1-endo is a potent inhibitor of the Wnt response, blocking a cell-based Wnt/??-catenin pathway reporter response with an IC50 value of 180 nM. Wnt proteins bind to receptors on the cell surface, initiating a signaling cascade that leads to ??-catenin activation of gene transcription.
More Information Supplier PageIWR-1-endo is a potent inhibitor of the Wnt response, blocking a cell-based Wnt/??-catenin pathway reporter response with an IC50 value of 180 nM. Wnt proteins bind to receptors on the cell surface, initiating a signaling cascade that leads to ??-catenin activation of gene transcription.
More Information Supplier PageEpoxomicin is a potent anti-tumor agent isolated from Actinomycetes that is used as a selective and irreversible inhibitor of the 20S proteasome.
More Information Supplier PageEpoxomicin is a potent anti-tumor agent isolated from Actinomycetes that is used as a selective and irreversible inhibitor of the 20S proteasome.
More Information Supplier PageEpoxomicin is a potent anti-tumor agent isolated from Actinomycetes that is used as a selective and irreversible inhibitor of the 20S proteasome.
More Information Supplier Page(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor.
More Information Supplier Page(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor.
More Information Supplier Page(+)-JQ1 is a potent, high affinity, selective BET bromodomain inhibitor.
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