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B288058-5mgPotent and selective SMYD2 inhibitor.
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B288376-25mgPotent and selective SMYD3 inhibitor.
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B288376-5mgPotent and selective SMYD3 inhibitor.
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B287674-25mgInactive control for BAY 678.
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B287674-5mgInactive control for BAY 678.
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B287148-25mgPotent and selective cell-permeable human neutrophil elastase (HNE) inhibitor.
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B287148-5mgPotent and selective cell-permeable human neutrophil elastase (HNE) inhibitor.
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B286864-10mgBAY-707 is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in
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B286864-25mgBAY-707 is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in
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B286864-50mgBAY-707 is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in
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B286864-5mgBAY-707 is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in
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B288179-25mgPotent Tie2 inhibitor.