Date published: 2025-9-17

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ZNF285A Inhibitors

Chemical inhibitors of ZNF285A include a variety of compounds that interfere with kinase activity and signaling pathways essential for the protein's function. Staurosporine is known to broadly inhibit protein kinases, which are crucial for phosphorylating proteins including ZNF285A. By inhibiting these kinases, staurosporine prevents the phosphorylation and subsequent activation of ZNF285A, leading to a functional inhibition of its activity. Bisindolylmaleimide I specifically targets Protein Kinase C (PKC), which is potentially responsible for modifying ZNF285A through phosphorylation. By inhibiting PKC, Bisindolylmaleimide I reduces the phosphorylation state of ZNF285A, leading to a decrease in its activity. Similarly, SP600125 acts as an inhibitor of c-Jun N-terminal kinase (JNK), which may regulate ZNF285A through phosphorylation-dependent mechanisms; thus, its inhibition can result in reduced ZNF285A function.

LY294002 targets phosphoinositide 3-kinases (PI3K), which are involved in various signaling pathways that could regulate the activity of ZNF285A. Inhibition by LY294002 can lead to a decrease in ZNF285A functional activity. PD98059 and U0126 both act as inhibitors of MEK, which is upstream of the ERK pathway, a crucial regulator in cellular signaling. The inhibition of this pathway by these chemicals can lead to the downregulation of ZNF285A activity. SB203580 inhibits p38 MAP kinase, potentially involved in the stress response that regulates ZNF285A. By inhibiting this kinase, SB203580 can prevent the activation of ZNF285A associated with the cellular stress response. PP2 targets Src family tyrosine kinases, which may be involved in the functional regulation of ZNF285A, leading to its inhibition upon the use of this chemical. PD173074 inhibits fibroblast growth factor receptors, which can be upstream regulators of signaling pathways that govern the activity of ZNF285A, and thus, its inhibition can lead to a decrease in ZNF285A activity. Y-27632 targets Rho-associated protein kinase, which, when inhibited, can lead to a reduction in ZNF285A activity if it is regulated by pathways involving this kinase. PD168393, by irreversibly inhibiting the epidermal growth factor receptor tyrosine kinase, can lead to the inhibition of ZNF285A if it lies downstream of the EGFR pathway. Lastly, Chelerythrine, another PKC inhibitor, ensures the functional inhibition of ZNF285A by reducing phosphorylation-mediated regulatory mechanisms.

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