Date published: 2025-9-18

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LOC653550 Inhibitors

Compounds like Wortmannin and U0126 can inhibit key signaling enzymes PI3K and MEK1/2, respectively, which can alter the activity of pathways that may be critical for the function of LOC653550. Trichostatin A, by inhibiting histone deacetylases, can change gene expression patterns, potentially affecting the transcriptional regulation of LOC653550. Rapamycin and Thapsigargin target fundamental cellular processes such as mTOR signaling and calcium homeostasis, which may indirectly influence the activity of LOC653550.

Imatinib and Cyclopamine, through their inhibition of specific tyrosine kinases and the Hedgehog pathway, respectively, can modulate signaling pathways that potentially intersect with the regulatory mechanisms of LOC653550. Bortezomib impacts protein turnover by inhibiting the proteasome, which could lead to an accumulation of proteins including LOC653550, if it is normally targeted for degradation. Retinoic Acid, all trans affects gene expression through the retinoic acid receptor-mediated pathway, offering another potential route to indirectly influence LOC653550 expression. Celecoxib, by inhibiting COX-2, can affect inflammatory signaling pathways and thus potentially the function of LOC653550 if it plays a role in inflammatory responses. DAPT, as a γ-secretase inhibitor, can impact the Notch signaling pathway, potentially affecting LOC653550 if it is part of this signaling cascade.

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