DUXA inhibitors are chemicals that indirectly lead to the inhibition of the transcription factor DUXA through various signaling pathways. These compounds are not direct antagonists of DUXA but inhibit upstream regulators or signaling pathways that contribute to DUXA's functional state. Staurosporine, for example, inhibits PKC and could impede the phosphorylation of DUXA, which is necessary for its activity. Inhibition of mTOR by rapamycin negatively affects the cellular conditions that promote DUXA activity, while LY294002 and Wortmannin decrease PI3K/AKT signaling, which could lead to reduced regulation of DUXA through AKT-dependent mechanisms.
In addition to these, MEK inhibitors like U0126 and PD98059 target the MAPK pathway, which is implicated in the regulation of various transcription factors, potentially including DUXA. SB203580's inhibition of p38 MAPK could also decrease DUXA activity by altering the transcription factor landscape in response to stress. JNK pathway inhibition by SP600125 may affect stress-related transcription factor activity, thereby indirectly influencing DUXA. Src kinase inhibition by PP2 might reduce DUXA activity by preventing activation of associated signaling cascades. Moreover, proteasome inhibition by Bortezomib can stabilize IκB, reducing NF-κB activity, which might intersect with DUXA regulatory
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