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S647748-5mgSIS3 free base is a potent and selective inhibitor of Smad3 phosphorylation. SIS3 free base inhibits the myofibroblast differentiation of fibroblasts by TGF-β1 . SIS3 free base does not affect the phosphorylation of Smad2In VitroSIS3 free base
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S655157-1mlSIS3 free base is a potent and selective inhibitor of Smad3 phosphorylation. SIS3 free base inhibits the myofibroblast differentiation of fibroblasts by TGF-β1 . SIS3 free base does not affect the phosphorylation of Smad2In VitroSIS3 free base
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S647079-100mgSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.Form:Solid
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S647079-10mgSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.Form:Solid
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S647079-25mgSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.Form:Solid
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S647079-50mgSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.Form:Solid
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S647079-5mgSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.Form:Solid
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S654859-1mlSJ000063181 is a potent BMP signaling activator with an EC 50 ≤1 µM. SJ000063181 can be used as chemical probes to interrogate BMP signaling due to it can penetrate zebrafish embryos.
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S649283-100mgSonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC 50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectivelyIn VitroThe IC 50 values for Sonidegib (NVP-LDE225) for the major human
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S649283-10mgSonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC 50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectivelyIn VitroThe IC 50 values for Sonidegib (NVP-LDE225) for the major human
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S649283-50mgSonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC 50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectivelyIn VitroThe IC 50 values for Sonidegib (NVP-LDE225) for the major human
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S649283-5mgSonidegib diphosphate (Erismodegib diphosphate) is a potent and selective Smo antagonist with IC 50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectivelyIn VitroThe IC 50 values for Sonidegib (NVP-LDE225) for the major human