Date published: 2025-9-30

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OTUB1 Activators

The chemical class termed OTUB1 Activators encompasses a range of compounds that can influence the activity of the OTUB1 protein, either directly or via modulation of associated cellular processes and pathways. Among the notable members of this class is cisplatin, a DNA damaging agent. The introduction of DNA damage by cisplatin can activate pathways where OTUB1 plays a role, thus indirectly influencing its activity. Similarly, etoposide, another compound in this class, induces DNA double-strand breaks. Such DNA damage stimulates pathways that can involve OTUB1, thereby affecting its function.

Hydrogen peroxide, which induces oxidative stress, is another significant member of this class. Oxidative stress can activate DNA repair pathways in which OTUB1 may participate. MG132, a proteasome inhibitor, can impact the ubiquitin-proteasome system, offering another avenue through which OTUB1's activity can be influenced. Chloroquine's role in altering autophagy showcases how changes in one cellular process can have a cascading effect, potentially affecting OTUB1 activity due to interconnected cellular pathways. 6-aminonicotinamide, as a PARP inhibitor, illustrates how interference in DNA repair pathways can have downstream effects on proteins like OTUB1. Agents like 5-fluorouracil and camptothecin, which respectively induce DNA damage and introduce DNA strand breaks, again underline the broad theme: disruption in DNA structure or replication dynamics can engage cellular repair mechanisms, subsequently influencing proteins, including OTUB1, associated with these processes.

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