Cyclin YL3 inhibitors are a class of chemical compounds that specifically target and inhibit the activity of cyclin YL3, a member of the cyclin family of proteins known for their role in regulating various aspects of the cell cycle and cellular signaling pathways. Unlike the more commonly studied cyclins involved in cell cycle progression, cyclin YL3 is associated with the regulation of specific signaling pathways, particularly those involved in cellular growth, differentiation, and response to extracellular signals. Cyclin YL3 forms complexes with cyclin-dependent kinases (CDKs), acting as a regulatory subunit that modulates the kinase activity of these enzymes. This interaction is critical for the phosphorylation of key substrates that govern cellular responses to growth factors and other signaling molecules.
Inhibitors of cyclin YL3 are typically designed to disrupt its interaction with CDKs or to interfere with its ability to bind to its substrates. These inhibitors may act by binding directly to cyclin YL3, blocking its ability to form functional complexes with CDKs, or by targeting the active sites involved in substrate recognition and phosphorylation. The design of cyclin YL3 inhibitors often involves detailed structural analysis of the protein to identify critical binding sites and interaction motifs. By inhibiting cyclin YL3, researchers can explore its specific role in cellular signaling pathways and gain insights into how its regulation affects cellular processes such as growth, differentiation, and response to environmental cues. The study of cyclin YL3 inhibitors provides valuable information about the broader functions of cyclins beyond cell cycle control, highlighting their involvement in intricate signaling networks that maintain cellular homeostasis and regulate responses to external stimuli. This research contributes to a deeper understanding of the diverse roles of cyclins in cellular biology and their potential as regulatory nodes in various signaling pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $321.00 | ||
CDK inhibitor that can arrest cell cycle progression, potentially causing downregulation of cyclin expression and activity. | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | $94.00 $265.00 | 42 | |
Inhibits CDKs, possibly leading to reduced phosphorylation and activation of cyclin partners, indirectly affecting cyclin function. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $259.00 | 41 | |
CDK inhibitor that could prevent activation of cyclin-CDK complexes, thereby influencing cyclin-mediated processes. | ||||||
Dinaciclib | 779353-01-4 | sc-364483 sc-364483A | 5 mg 25 mg | $247.00 $888.00 | 1 | |
Strongly inhibits CDKs, possibly impacting cyclin function by preventing the activation of its CDK partners. | ||||||
PHA-848125 | 802539-81-7 | sc-364581 sc-364581A | 5 mg 10 mg | $304.00 $555.00 | ||
Targets multiple CDKs and could influence cyclin functions by altering CDK activity and the cell cycle. | ||||||
Ribociclib | 1211441-98-3 | sc-507367 | 10 mg | $450.00 | ||
Inhibits CDK4/6, possibly affecting downstream cyclin D processes, which could indirectly influence Cyclin YL3 activity if related. | ||||||
Abemaciclib | 1231929-97-7 | sc-507342 | 10 mg | $110.00 | ||
Selectively inhibits CDK4/6, potentially altering the activity of cyclins by inhibiting their associated kinases. | ||||||
SNS-032 | 345627-80-7 | sc-364621 sc-364621A | 5 mg 10 mg | $169.00 $262.00 | ||
Binds to CDKs, potentially altering cyclin activity by preventing necessary phosphorylation events. | ||||||
AZD 5438 | 602306-29-6 | sc-361115 sc-361115A | 10 mg 50 mg | $205.00 $865.00 | ||
Inhibits CDKs, which could indirectly alter cyclin activity by affecting the cell cycle and associated signaling pathways. | ||||||
AT-7519 Hydrochloride | 902135-91-5 | sc-482715 | 5 mg | $125.00 | ||
Inhibits multiple CDKs, potentially modulating the activity of cyclins through disruption of their interaction with CDK partners. | ||||||