Sorafenib tosylate is a potent inhibitor of Raf-1 with IC50 values of 6 nM, 22 nM and 90 nM for Raf-1, B-Raf, and VEGFR2 respectively. Sorafenib tosylate suppresses both wild-type and V599E mutant BRAF activity in vitro.
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Amlexanox is a selective inhibitor of TBK1 and IKKε with IC50 values of ~1-2 μM.
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Amlexanox is a selective inhibitor of TBK1 and IKKε with IC50 values of ~1-2 μM.
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Amlexanox is a selective inhibitor of TBK1 and IKKε with IC50 values of ~1-2 μM.
More Information Supplier Page Amlexanox is a selective inhibitor of TBK1 and IKKε with IC50 values of ~1-2 μM.
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AG-1478 selectively inhibits EGFR with IC50 of 3 nM in cell-free assay.
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AG-1478 selectively inhibits EGFR with IC50 of 3 nM in cell-free assay.
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Sorafenib tosylate is a potent inhibitor of Raf-1 with IC50 values of 6 nM, 22 nM and 90 nM for Raf-1, B-Raf, and VEGFR2 respectively. Sorafenib tosylate suppresses both wild-type and V599E mutant BRAF activity in vitro.
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Sorafenib tosylate is a potent inhibitor of Raf-1 with IC50 values of 6 nM, 22 nM and 90 nM for Raf-1, B-Raf, and VEGFR2 respectively. Sorafenib tosylate suppresses both wild-type and V599E mutant BRAF activity in vitro.
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Tripelennamine HCl is an antagonist of H1-receptor that used as a psychoactive drug with antipruritic activity.
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