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K647952-1mgKetoconazole-d 4 is the deuterium labeled Ketoconazole. Ketoconazole (R-41400) is an imidazole anti-fungal agent, a CYP3A4 and CYP24A1 inhibitor.In VitroStable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug
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K124652-100mgKetotifen Fumarate.
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K124652-1gKetotifen Fumarate.
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K124652-250mgKetotifen Fumarate.
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K124652-25gKetotifen Fumarate.
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K124652-5gKetotifen Fumarate.
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K648903-1mgKFM19 is a potent, selective Adenosine receptor ( A1-receptor ) antagonist, with an IC 50 of 50 nM.Form:SolidIC50&: Target:IC50: 50 nM (Adenosine receptor).
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K648903-5mgKFM19 is a potent, selective Adenosine receptor ( A1-receptor ) antagonist, with an IC 50 of 50 nM.Form:SolidIC50&: Target:IC50: 50 nM (Adenosine receptor).
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K651370-10mgKH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC 50 value of 0.35 μM. KH-3 has anti-proliferative activity. KH-3 suppresses breast cancer cell invasion as well as delays the initiation of lung colonies by disrupting
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K651370-25mgKH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC 50 value of 0.35 μM. KH-3 has anti-proliferative activity. KH-3 suppresses breast cancer cell invasion as well as delays the initiation of lung colonies by disrupting
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K651370-5mgKH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC 50 value of 0.35 μM. KH-3 has anti-proliferative activity. KH-3 suppresses breast cancer cell invasion as well as delays the initiation of lung colonies by disrupting
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K650174-10mgKI696 is a high affinity probe that disrupts the Keap1/NRF2 interaction. KI696 is a potent and selective inhibitor of the KEAP1 / NRF2 interactionIn VitroKI696 (compound 7) exhibits very high affinity for the KEAP1 Kelch domain (ITC K d =1.3 nM with