Cdc25C inhibitors belong to a specific chemical class known for their capacity to modulate the activity of Cell Division Cycle 25C (Cdc25C), a phosphatase enzyme that regulates cell cycle progression by dephosphorylating critical target proteins. These inhibitors function by interfering with the interactions involving Cdc25C, which is a pivotal player in controlling cell cycle checkpoints and promoting cell division. Cdc25C plays a central role in coordinating cell cycle transitions, particularly the G2/M phase transition, by activating cyclin-dependent kinases. Cdc25C inhibitors are thoughtfully designed to target specific binding sites or molecular pathways associated with Cdc25C, thus influencing its cellular functions and downstream effects.
The development of Cdc25C inhibitors necessitates a comprehensive understanding of the structural attributes of Cdc25C and its interactions with substrates and regulatory proteins. Researchers in this field strive to engineer molecules with high selectivity and affinity for Cdc25C, allowing for precise modulation of its activities. These inhibitors often employ innovative design strategies that disrupt key molecular interactions required for Cdc25C's catalytic function. By gaining insights into the intricate mechanisms through which Cdc25C participates in cell cycle regulation and progression, researchers aim to unravel its significance in fundamental cellular processes. The ongoing advancements in molecular pharmacology and chemical synthesis drive the refinement of Cdc25C inhibitors, offering applications across diverse scientific domains where manipulation of Cdc25C-mediated processes is of interest.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NSC 95397 | 93718-83-3 | sc-203654 sc-203654A | 10 mg 50 mg | $255.00 $847.00 | 9 | |
NSC 95397 inhibits CDC25C by blocking its phosphatase activity towards CDK1, resulting in cell cycle arrest and suppression of tumor cell proliferation and division. | ||||||
2-Amino-3-chloro-1,4-naphthoquinone | 2797-51-5 | sc-470529 sc-470529A | 25 g 500 g | $71.00 $653.00 | ||
2-Amino-3-chloro-1,4-naphthoquinone targets CDC25C to prevent CDK1 activation, resulting in G2/M phase arrest and suppressed cell proliferation, making it a potential candidate for anti-cancer therapy. | ||||||
CDC25 Phosphatase Inhibitor II, NSC 663284 | 383907-43-5 | sc-202987A sc-202987 sc-202987B sc-202987C | 1 mg 5 mg 10 mg 25 mg | $51.00 $241.00 $357.00 $663.00 | 4 | |
NSC 663248 inhibits CDC25C activity, leading to CDK1 inactivation, G2/M arrest, and impaired cell division, offering potential therapeutic benefits in cancer research. | ||||||
Butyrolactone I | 87414-49-1 | sc-201533 sc-201533A | 200 µg 1 mg | $122.00 $514.00 | 1 | |
Butyrolactone I inhibits CDC25C, causing G2/M cell cycle arrest by blocking CDK1 activation, thus exhibiting potential anti-cancer properties through cell growth suppression. | ||||||
Triapine | 200933-27-3 | sc-475303 | 10 mg | $300.00 | ||
Triapine interferes with CDC25C-mediated CDK1 dephosphorylation, causing G2/M arrest and impairing cell cycle progression, contributing to its potential anti-cancer effects. | ||||||