Date published: 2025-9-12

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LOC728804 Inhibitors

Trichostatin A and 5-Azacytidine are epigenetic modulators that alter gene expression, which can change the synthesis patterns of proteins. MG132, a proteasome inhibitor, could prevent the degradation of proteins, potentially causing an accumulation of a target protein within the cell. Staurosporine, a kinase inhibitor, has the ability to disrupt phosphorylation events, which are crucial for the regulation of protein activity and signaling pathways, thereby potentially altering the activity of a protein like LOC728804.

Brefeldin A impedes protein transport by disrupting the Golgi apparatus, which could affect the maturation and trafficking of proteins. Cycloheximide halts protein synthesis, leading to a decrease in the production of new proteins within the cell. The glycolysis inhibitor 2-Deoxy-D-glucose could create an energy deficit, influencing proteins involved in energy-dependent processes. Compounds like β-Catenin/Tcf Inhibitor, FH535, which inhibits Wnt/β-catenin signaling, PD173074, an FGFR tyrosine kinase inhibitor, and LY294002, a PI3K inhibitor, affect growth factor signaling and cellular proliferation pathways. Such inhibitors could therefore modulate the expression or function of proteins involved in these pathways. Rapamycin targets the mTOR pathway, which is integral to cell growth and protein synthesis, and could thereby influence the synthesis and activity of a protein like LOC728804. Furthermore, Y-27632, which inhibits the Rho-associated protein kinase (ROCK), could alter cell morphology and signaling, potentially affecting the signaling pathways or structural contexts in which LOC728804 operates.

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