Date published: 2025-9-13

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RDM1 Activators

Resveratrol targets SIRT1, an enzyme that deacetylates proteins, potentially impacting DNA repair activities in which RDM1 is involved. Curcumin, another multifaceted compound, interacts with various signaling pathways, including those integral to DNA repair, thereby potentially modulating RDM1's role in maintaining genomic integrity. Sulforaphane, a compound known to activate the Nrf2 pathway, can lead to the expression of protective genes that might intersect with the pathways involving RDM1. Similarly, the flavonoid quercetin, by influencing the activity of topoisomerase II, could alter the DNA topology and affect RDM1's engagement with DNA repair mechanisms. The isoflavone genistein, known for its role in cell signaling modulation, also touches upon DNA repair processes, possibly influencing RDM1's function.

Compounds like epigallocatechin gallate possess the capability to modulate numerous signaling molecules and pathways, some of which are likely to cross paths with DNA repair processes involving RDM1. Caffeine, a well-known inhibitor of ATM and ATR kinases, impacts the cellular response to DNA damage, which is a response in which RDM1 is a participant. The impact of caffeine illustrates how modulation of the DNA damage response can have implications for proteins involved in DNA repair. The kinase inhibitors U0126 and LY294002, which target MEK and PI3K respectively, demonstrate the interconnectedness of cell signaling and DNA repair, as they can affect MAPK and AKT signaling pathways, potentially influencing RDM1 activity. Rapamycin, an mTOR inhibitor, and Olaparib, a PARP inhibitor, also play roles in the regulation of DNA repair mechanisms, suggesting a possible link to RDM1 activity.

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