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2 protocols using sb259063

1

Inhibitors and Activators of Key Signaling Pathways

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Tumor Necrosis Factor‐alpha (TNF‐α), Transforming Growth Factor beta 1 (TGFβ1), Transforming Growth Factor beta 2 (TGFβ2) and Interleukin 6 (IL‐6) were purchased from PeproTech (Rocky Hill, NJ, USA). Recombinant human VEGF 165 protein was purchased from R&D Systems (Minneapolis, MN, USA). Aflibercept (Eylea) was purchased from Regeneron Pharmaceuticals (Tarrytown, NY, USA). d‐glucose, mannitol, L‐glucose, and RUNX1 inhibitor Ro5‐3335 were purchased from Millipore‐Sigma (Burlington, MA, USA). Small‐molecule inhibitors and activators purchased from commercial sources included TNF‐α‐TNFR1 binding inhibitor CAY10500 and JNK activator anisomycin, (Santa Cruz Biotechnology, Dallas, TX, USA); NF‐κB inhibitors Caffeic acid phenethyl ester (CAPE) and Honokiol; dual NF‐κB and JNK inhibitor Withaferin A, JNK inhibitors SP600125 and TCS JNK 6o; p38/MAPK inhibitors SB259063 and SB202190 (Tocris Bioscience, Bristol, UK); and AP‐1 inhibitor, SR11302 (R&D Systems). The CBFβ‐RUNX1 protein–protein interaction inhibitor, AI‐14‐91, and an inactive control compound of similar chemical structure, AI‐4‐88, were synthesized as described previously.36
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2

Modulation of Signaling Pathways in Cell Culture

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Tumor Necrosis Factor alpha (TNF-α), Transforming Growth Factor beta 1 (TGFβ1), Transforming Growth Factor beta 2 (TGFβ2) and Interleukin 6 (IL-6) were purchased from PeproTech (Rocky Hill, NJ, USA). Recombinant human VEGF 165 protein was purchased from R&D Systems (Minneapolis, MN, USA). Aflibercept (Eylea) was purchased from Regeneron Pharmaceuticals (Tarrytown, NY, USA). D-glucose, mannitol, L-glucose and RUNX1 inhibitor Ro5–3335 were purchased from Millipore-Sigma (Burlington, MA, USA). Small molecule inhibitors and activators purchased from commercial sources included TNF-α-TNFR1 binding inhibitor CAY10500 and JNK activator anisomycin, (Santa Cruz Biotechnology, Dallas, TX, USA); NF-κB inhibitors Caffeic acid phenethyl ester (CAPE) and Honokiol; dual NF-κB and JNK inhibitor Withaferin A, JNK inhibitors SP600125 and TCS JNK 6o; p38/MAPK inhibitors SB259063 and SB202190 (Tocris Bioscience, Bristol, UK); and AP-1 inhibitor, SR11302 (R&D Systems). The CBFβ-RUNX1 protein-protein interaction inhibitor, AI-14–91, and an inactive control compound of similar chemical structure, AI-4–88, were synthesized as described previously [36 (link)].
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