The chemical class termed ZNF175 Inhibitors focuses on indirectly modulating the activity or influence of ZNF175 through a variety of molecular pathways, mainly due to the current absence of direct inhibitors. The class encompasses a range of compounds from bromodomain inhibitors like JQ1 to histone deacetylase inhibitors such as SAHA. The primary goal is to target either the epigenetic landscape or associated signaling networks to exert influence on ZNF175's biological activities. For instance, JQ1 and A-485 target the reading and writing of epigenetic marks, respectively. These inhibitors, by modulating the chromatin state, can indirectly affect the functions ZNF175 may have in transcriptional regulation or other chromatin-based processes.
Several inhibitors on this list act by affecting signaling pathways or other cellular mechanisms associated with ZNF175. For example, Wnt-C59 targets the Wnt signaling pathway, while LY294002 is a broad-spectrum inhibitor affecting the PI3K pathway. SR-95531 is unique in targeting neurotransmitter receptors, thus possibly implicating ZNF175 in such signaling if a relationship exists. Despite the indirect nature of these inhibitors, their to influence ZNF175 is built on logical mechanistic assumptions rooted in the cellular and molecular pathways the protein is presumed to be involved in. Further research is warranted to confirm these associations and to develop direct inhibitors of ZNF175.
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