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16679-5A potent inhibitor of the kinase activity of ALK2 (IC<sub>50</sub> = 13-108 nM) disrupts dorsoventral development in zebrafish affects stem cell development, increasing cardiomyocyte progenitors and promoting neurogenesis inhibits the growth of
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19571-10A 1,4-naphthoquinone that acts as a redox-cycling agent, typically increasing intracellular superoxide and hydrogen peroxide formation.
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19571-25A 1,4-naphthoquinone that acts as a redox-cycling agent, typically increasing intracellular superoxide and hydrogen peroxide formation.
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19571-5A 1,4-naphthoquinone that acts as a redox-cycling agent, typically increasing intracellular superoxide and hydrogen peroxide formation.
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71210-10A cell permeable, competitive inhibitor of HIF-1&alpha prolyl hydroxylase stabilizes HIF-1&alpha expression at normal oxygen tensions in cultured cells at concentrations between 0.1 and 1 mM.
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71210-100A cell permeable, competitive inhibitor of HIF-1&alpha prolyl hydroxylase stabilizes HIF-1&alpha expression at normal oxygen tensions in cultured cells at concentrations between 0.1 and 1 mM.
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71210-50A cell permeable, competitive inhibitor of HIF-1&alpha prolyl hydroxylase stabilizes HIF-1&alpha expression at normal oxygen tensions in cultured cells at concentrations between 0.1 and 1 mM.
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71210-500A cell permeable, competitive inhibitor of HIF-1&alpha prolyl hydroxylase stabilizes HIF-1&alpha expression at normal oxygen tensions in cultured cells at concentrations between 0.1 and 1 mM.
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10006436-1A commonly-used spin trap that reacts with O-, N-, S-, and C-centered radicals, allowing their characterization by electron spin resonance and immuno-spin trapping is water-soluble, rapidly penetrates lipid bilayers, has low toxicity, and can be
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10006436-5A commonly-used spin trap that reacts with O-, N-, S-, and C-centered radicals, allowing their characterization by electron spin resonance and immuno-spin trapping is water-soluble, rapidly penetrates lipid bilayers, has low toxicity, and can be
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10006436-500A commonly-used spin trap that reacts with O-, N-, S-, and C-centered radicals, allowing their characterization by electron spin resonance and immuno-spin trapping is water-soluble, rapidly penetrates lipid bilayers, has low toxicity, and can be
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17551-1A potent inhibitor of human PDGFR&beta (IC<sub>50</sub> = 80 nM).