PSE1 inhibitors are a class of chemical compounds designed to selectively interfere with the activity of the PSE1 protein, which plays a key role in cellular processes such as nuclear transport and intracellular signaling. The PSE1 protein, part of the importin-β family, is involved in the import of cargo proteins into the nucleus by interacting with nuclear localization signals. Inhibitors targeting PSE1 typically work by binding to specific regions of the protein, thereby disrupting its normal interactions and transport mechanisms. This inhibition can provide insight into the regulatory mechanisms that govern nuclear-cytoplasmic transport and other related cellular functions.
Chemically, PSE1 inhibitors can be diverse, ranging from small organic molecules to larger peptides or even modified nucleic acids, depending on the approach used to inhibit the protein. The structural design of these inhibitors is often focused on achieving high specificity and affinity for the PSE1 protein, ensuring that they effectively block its function without off-target effects. These inhibitors may interact with different domains of PSE1, such as the Ran-binding site or cargo-binding regions, leading to distinct modes of inhibition, such as competitive or allosteric inhibition. By inhibiting PSE1, researchers can explore the downstream effects on nuclear transport, gene expression, and overall cellular homeostasis. The development of PSE1 inhibitors not only aids in dissecting the protein's function but also serves as a valuable tool in studying the broader network of nuclear transport processes and their implications in cellular biology.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Leptomycin B | 87081-35-4 | sc-358688 sc-358688A sc-358688B | 50 µg 500 µg 2.5 mg | $107.00 $416.00 $1248.00 | 35 | |
An inhibitor of CRM1/exportin 1, impacting nuclear export but can indirectly influence nuclear import dynamics. | ||||||
KPT 330 | 1393477-72-9 | sc-489062 | 5 mg | $173.00 | ||
An inhibitor of nuclear export by targeting CRM1, affecting nuclear transport dynamics. | ||||||
Mifepristone | 84371-65-3 | sc-203134 | 100 mg | $61.00 | 17 | |
While primarily a glucocorticoid receptor antagonist, it can influence nuclear-cytoplasmic shuttling, potentially affecting PSE1 pathways. | ||||||
Ratjadone A, Synthetic | 163564-92-9 | sc-203234 | 2 µg | $168.00 | 2 | |
Alters CRM1-mediated nuclear export, indirectly affecting nuclear transport dynamics related to PSE1. | ||||||
Verdinexor | 1392136-43-4 | sc-492602 | 5 mg | $395.00 | ||
A selective inhibitor of nuclear export, potentially influencing PSE1-associated nuclear import. | ||||||