Date published: 2025-9-17

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MsrB3 Inhibitors

MsrB3 inhibitors, as conceived, comprise compounds that can either directly modulate the enzymatic activity of MsrB3 or indirectly influence its functionality via perturbation of associated pathways or the cellular redox state. Given the absence of specific MsrB3-targeting compounds, the selected molecules are found in a strategic understanding of its role in the oxidative stress response and its interconnectedness with other redox-active systems.

For instance, Auranofin's inhibition of thioredoxin reductase can hinder the function of many Msr enzymes, given their reliance on reduced thioredoxins. Similarly, agents like BCNU can interfere at a broader level, affecting MsrB3 by disrupting general protein functionality. Shifting the cellular redox balance using compounds like Methylene Blue or Plumbagin provides another angle of modulation, given that an imbalance in either direction (oxidative or reductive stress) could challenge MsrB3's typical operations. Moreover, molecules like Ebselen, which mimic other antioxidant enzyme activities, provide a means of indirectly modulating MsrB3 by shifting the overall redox equilibrium in cells. The comprehensive understanding of these inhibitors underscores the intricate web of interactions and dependencies in the cellular redox landscape and the points of intervention to modulate MsrB3's role therein.

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