Cdc14 inhibitors are a class of chemical compounds specifically designed to inhibit the activity of the Cdc14 phosphatase, an enzyme that plays a critical role in regulating various stages of the cell cycle. Cdc14 is a conserved protein phosphatase involved in processes such as mitotic exit, cytokinesis, and the dephosphorylation of key substrates that control the progression of cell division. By reversing phosphorylation on specific proteins, Cdc14 ensures proper cell cycle transitions, particularly from mitosis to the G1 phase. Inhibitors of Cdc14 target its enzymatic activity, binding to the active site or other regulatory regions, thus preventing it from removing phosphate groups from its substrate proteins. By blocking Cdc14's function, these inhibitors disrupt its regulatory effects on the cell cycle, offering insight into the molecular mechanisms governing cell division.
The chemical design of Cdc14 inhibitors typically involves molecules that interact with key catalytic or regulatory residues within the phosphatase's active site. These inhibitors may form hydrogen bonds, ionic interactions, or van der Waals forces to stabilize their binding and prevent the phosphatase from accessing its natural substrates. Cdc14 inhibitors can act competitively, where they directly compete with the substrate for binding at the active site, or non-competitively, by binding to allosteric sites that induce conformational changes, reducing the enzyme's catalytic efficiency. The development and optimization of these inhibitors often involve techniques such as molecular docking, high-throughput screening, and X-ray crystallography to enhance their specificity and binding affinity. By inhibiting Cdc14, these compounds provide valuable tools for studying cell cycle regulation, particularly the complex network of phosphorylation and dephosphorylation events that ensure accurate and timely progression through different phases of the cell cycle.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Olomoucine | 101622-51-9 | sc-3509 sc-3509A | 5 mg 25 mg | $72.00 $274.00 | 12 | |
A CDK inhibitor that might influence Cdc14 by modifying cell cycle progression. | ||||||
Siomycin A | 12656-09-6 | sc-202339 sc-202339-CW sc-202339A sc-202339B | 500 µg 500 µg 2.5 mg 25 mg | $439.00 $449.00 $1326.00 $10200.00 | 4 | |
A thiazole compound that inhibits the FOXM1 transcription factor, potentially altering the expression of genes involved in mitotic exit and Cdc14 regulation. | ||||||
Purvalanol A | 212844-53-6 | sc-224244 sc-224244A | 1 mg 5 mg | $71.00 $291.00 | 4 | |
A potent CDK inhibitor that may impact Cdc14 by affecting upstream regulatory pathways involved in mitosis. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $76.00 $255.00 | 18 | |
An inhibitor of ribonucleotide reductase that leads to DNA replication stress, potentially affecting cell cycle progression and Cdc14 activity. | ||||||
Monastrol | 254753-54-3 | sc-202710 sc-202710A | 1 mg 5 mg | $120.00 $233.00 | 10 | |
A kinesin Eg5 inhibitor leading to mitotic arrest, which could potentially impact the regulation of Cdc14. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
An inhibitor of JNK kinase that might have an impact on cell cycle regulatory networks affecting Cdc14. | ||||||
UCN-01 | 112953-11-4 | sc-202376 | 500 µg | $246.00 | 10 | |
A kinase inhibitor that affects multiple targets, potentially altering Cdc14 activity through its role in cell cycle control. | ||||||
Alsterpaullone | 237430-03-4 | sc-202453 sc-202453A | 1 mg 5 mg | $67.00 $306.00 | 2 | |
An inhibitor of glycogen synthase kinase-3β (GSK-3β) that might affect Cdc14 activity through indirect pathways involved in cell cycle regulation. | ||||||
Mitoxantrone | 65271-80-9 | sc-207888 | 100 mg | $279.00 | 8 | |
An antineoplastic agent that causes DNA damage and can influence cell cycle progression, potentially affecting Cdc14 activity. | ||||||