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17382-25A-66 is a potent, selective inhibitor of the PI3K isoform p110&alpha (IC<sub>50</sub> = 32 nM in a cell-free assay). It displays over 100-fold selectivity for p110&alpha over other isoforms.
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17382-5A-66 is a potent, selective inhibitor of the PI3K isoform p110&alpha (IC<sub>50</sub> = 32 nM in a cell-free assay). It displays over 100-fold selectivity for p110&alpha over other isoforms.
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9001799-1An inhibitor of ALK5, ALK4, and ALK7 (IC<sub>50</sub>s = 12, 45, and 7.5 nM, respectively) blocks the phosphorylation of Smad2/3 and inhibits TGF-&beta-induced epithelial-to-mesenchymal transition used to reprogram fibroblasts into alternative
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9001799-10An inhibitor of ALK5, ALK4, and ALK7 (IC<sub>50</sub>s = 12, 45, and 7.5 nM, respectively) blocks the phosphorylation of Smad2/3 and inhibits TGF-&beta-induced epithelial-to-mesenchymal transition used to reprogram fibroblasts into alternative
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9001799-25An inhibitor of ALK5, ALK4, and ALK7 (IC<sub>50</sub>s = 12, 45, and 7.5 nM, respectively) blocks the phosphorylation of Smad2/3 and inhibits TGF-&beta-induced epithelial-to-mesenchymal transition used to reprogram fibroblasts into alternative
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9001799-5An inhibitor of ALK5, ALK4, and ALK7 (IC<sub>50</sub>s = 12, 45, and 7.5 nM, respectively) blocks the phosphorylation of Smad2/3 and inhibits TGF-&beta-induced epithelial-to-mesenchymal transition used to reprogram fibroblasts into alternative
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16415-1An enzyme-activated, irreversible inhibitor of the arginine decarboxylases of E. coli (Ki = 800 µM), P.
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16415-10An enzyme-activated, irreversible inhibitor of the arginine decarboxylases of E. coli (Ki = 800 µM), P.
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16415-25An enzyme-activated, irreversible inhibitor of the arginine decarboxylases of E. coli (Ki = 800 µM), P.
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16415-5An enzyme-activated, irreversible inhibitor of the arginine decarboxylases of E. coli (Ki = 800 µM), P.
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18317-1A selective inhibitor of SUV420H1 and SUV420H2 (IC<sub>50</sub>s = 25 and 144 nM, respectively) that inhibits the di- and trimethylation of H4K20me in multiple cell lines.
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18317-5A selective inhibitor of SUV420H1 and SUV420H2 (IC<sub>50</sub>s = 25 and 144 nM, respectively) that inhibits the di- and trimethylation of H4K20me in multiple cell lines.