Date published: 2025-9-21

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KRTAP4-11 Inhibitors

KRTAP4-11 inhibitor Disulfiram's alteration of the redox state can affect protein structures sensitive to redox changes, including KRTAP4-11. Alizarin's interaction with calcium ions can disrupt KRTAP4-11, which may be affected by calcium levels. Mitomycin C's action on DNA may impede the replication and transcription of KRTAP4-11's gene. MG-132's inhibition of the ubiquitin-proteasome pathway can lead to an accumulation of proteins, thereby influencing the degradation of KRTAP4-11. Cycloheximide acts by halting protein synthesis, which directly impacts the production of new KRTAP4-11 protein. Actinomycin D suppresses RNA synthesis, thereby affecting KRTAP4-11 at the transcriptional level. Staurosporine and Sodium orthovanadate target phosphorylation processes, which can modify the phosphorylation state of KRTAP4-11, influencing its activity and interactions.

Brefeldin A's disruption of protein transport affects the intracellular localization and secretion of KRTAP4-11, while Nocodazole's destabilization of microtubules can impact the overall cellular architecture and distribution of proteins like KRTAP4-11. The glycolytic pathway, when inhibited by 2-Deoxy-D-glucose, can alter the energy balance of the cell, which is crucial for the synthesis and maintenance of proteins, potentially affecting KRTAP4-11 levels. Lithium chloride's inhibition of GSK-3 may impact Wnt signaling, thus influencing the expression patterns of proteins such as KRTAP4-11.

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