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G127955-100mgGSK1059615 is a dual inhibitor of PI3Kα/β/δ/γ (reversible) and mTOR with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM, respectively.A potent inhibitor of PI 3-kinase and FRAP (mTOR).
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G127955-25mgGSK1059615 is a dual inhibitor of PI3Kα/β/δ/γ (reversible) and mTOR with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM, respectively.A potent inhibitor of PI 3-kinase and FRAP (mTOR).
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G127955-5mgGSK1059615 is a dual inhibitor of PI3Kα/β/δ/γ (reversible) and mTOR with IC50 of 0.4 nM/0.6 nM/2 nM/5 nM and 12 nM, respectively.A potent inhibitor of PI 3-kinase and FRAP (mTOR).
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G127938-100mgGSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >:100-fold selectivity against the closely related Aurora A-TPX2 complex.
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G127938-10mgGSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >:100-fold selectivity against the closely related Aurora A-TPX2 complex.
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G127938-25mgGSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >:100-fold selectivity against the closely related Aurora A-TPX2 complex.
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G127938-50mgGSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >:100-fold selectivity against the closely related Aurora A-TPX2 complex.
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G127938-5mgGSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3.5 nM/6.5 nM. It displays >:100-fold selectivity against the closely related Aurora A-TPX2 complex.
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G124898-10mgGSK126 is a potent highly selective S adenosyl methionine competitive small molecule inhibitor of EZH2 methyltransferase with Ki value of 0.5 nM.
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G124898-50mgGSK126 is a potent highly selective S adenosyl methionine competitive small molecule inhibitor of EZH2 methyltransferase with Ki value of 0.5 nM.
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G124898-5mgGSK126 is a potent highly selective S adenosyl methionine competitive small molecule inhibitor of EZH2 methyltransferase with Ki value of 0.5 nM.
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