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A607294-10mgA-395 is an antagonist of polycomb repressive complex 2 (PRC2) protein-protein interactions that potently inhibits the trimeric PRC2 complex (EZH2-EED-SUZ12, IC50: 18 nM).
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A607294-1mgA-395 is an antagonist of polycomb repressive complex 2 (PRC2) protein-protein interactions that potently inhibits the trimeric PRC2 complex (EZH2-EED-SUZ12, IC50: 18 nM).
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A607294-25mgA-395 is an antagonist of polycomb repressive complex 2 (PRC2) protein-protein interactions that potently inhibits the trimeric PRC2 complex (EZH2-EED-SUZ12, IC50: 18 nM).
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A607294-5mgA-395 is an antagonist of polycomb repressive complex 2 (PRC2) protein-protein interactions that potently inhibits the trimeric PRC2 complex (EZH2-EED-SUZ12, IC50: 18 nM).
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A274865-10mgStore at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.
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A274865-50mgStore at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.
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A126060-10mgA-443654 is a potent small-molecule inhibitor of all three Akt serine/threonine kinases, induces Akt Ser-473 phosphorylation in all human cancer cell lines tested, including PTEN- and TSC2-deficient lines.
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A126060-25mgA-443654 is a potent small-molecule inhibitor of all three Akt serine/threonine kinases, induces Akt Ser-473 phosphorylation in all human cancer cell lines tested, including PTEN- and TSC2-deficient lines.
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A126060-50mgA-443654 is a potent small-molecule inhibitor of all three Akt serine/threonine kinases, induces Akt Ser-473 phosphorylation in all human cancer cell lines tested, including PTEN- and TSC2-deficient lines.
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A126060-5mgA-443654 is a potent small-molecule inhibitor of all three Akt serine/threonine kinases, induces Akt Ser-473 phosphorylation in all human cancer cell lines tested, including PTEN- and TSC2-deficient lines.
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A126845-100mgA-674563 is an Akt1 inhibitor with Ki of 11 nM in cell-free assays, modest potent to PKA and >:30-fold selective for Akt1 over PKC.A selective Akt1, PKA, and CDK2 inhibitor.
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A126845-25mgA-674563 is an Akt1 inhibitor with Ki of 11 nM in cell-free assays, modest potent to PKA and >:30-fold selective for Akt1 over PKC.A selective Akt1, PKA, and CDK2 inhibitor.