PCTAIRE-3 inhibitors, also known as cyclin-dependent kinase 16 (CDK16) inhibitors, constitute a class of small molecules specifically designed to target and modulate the activity of the PCTAIRE-3 protein kinase. PCTAIRE-3 belongs to the PCTAIRE family of kinases and plays a crucial role in cell cycle regulation and various cellular processes. The inhibitors in this class are primarily developed to study the underlying mechanisms of PCTAIRE-3 and its involvement in fundamental cellular activities.These inhibitors exert their effects by binding to the active site of PCTAIRE-3, which is an ATP-binding pocket. By occupying this binding site, PCTAIRE-3 inhibitors interfere with the kinase's ability to phosphorylate its target substrates.
This disruption in phosphorylation cascades can lead to downstream consequences in the cell cycle and other signaling pathways. Consequently, these inhibitors are valuable tools in both basic and translational research to investigate the precise functions of PCTAIRE-3 in cellular biology. Researchers utilize PCTAIRE-3 inhibitors to gain insights into the molecular and cellular processes regulated by this kinase. Their mechanisms of action extend beyond PCTAIRE-3 inhibition, often affecting other cyclin-dependent kinases (CDKs) as well. This broadens their utility in exploring the roles of multiple CDKs in various cellular functions. PCTAIRE-3 inhibitors, as a class of chemical compounds, have thus become essential in elucidating the intricate interplay of CDKs in cell cycle control, gene expression, and cell signaling pathways, ultimately advancing our understanding of fundamental biological processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
RO-3306 | 872573-93-8 | sc-358700 sc-358700A sc-358700B | 1 mg 5 mg 25 mg | $65.00 $160.00 $320.00 | 37 | |
Ro-3306 is a selective ATP-competitive inhibitor of PCTAIRE-3 (CDK16). It inhibits PCTAIRE-3 by binding to its ATP-binding site, blocking phosphorylation and regulating cell cycle progression. | ||||||
AZD 5438 | 602306-29-6 | sc-361115 sc-361115A | 10 mg 50 mg | $205.00 $865.00 | ||
AZD5438 is a potent inhibitor of several CDKs, including PCTAIRE-3. It functions by preventing CDK activity and the subsequent cell cycle progression. | ||||||
Indirubin-3′-monoxime | 160807-49-8 | sc-202660 sc-202660A sc-202660B | 1 mg 5 mg 50 mg | $77.00 $315.00 $658.00 | 1 | |
Indirubin-3'-monoxime inhibits PCTAIRE-3 by competing for ATP binding, disrupting its kinase activity. It has been studied for its potential in suppressing cell proliferation and tumor growth. | ||||||
SNS-032 | 345627-80-7 | sc-364621 sc-364621A | 5 mg 10 mg | $169.00 $262.00 | ||
SNS-032 is a selective inhibitor of CDK2, CDK7, and CDK9, including PCTAIRE-3. It disrupts CDK-dependent phosphorylation, leading to cell cycle arrest and antitumor effects. | ||||||
1-Naphthyl PP1 | 221243-82-9 | sc-203765 sc-203765A | 10 mg 50 mg | $230.00 $964.00 | 3 | |
1-Naphthyl PP1 is an ATP-competitive inhibitor that targets PCTAIRE-3. It binds to the ATP-binding site, inhibiting kinase activity and cell cycle progression, particularly in cancer cells. | ||||||
SU 9516 | 377090-84-1 | sc-222330 sc-222330A | 5 mg 25 mg | $122.00 $383.00 | 3 | |
SU9516 is a small molecule inhibitor of CDK2 and CDK1, including PCTAIRE-3. It blocks kinase activity, resulting in cell cycle arrest. | ||||||
Polo-like Kinase Inhibitor III | 660868-91-7 | sc-203202 | 500 µg | $107.00 | 1 | |
GW843682X is a potent CDK2 and CDK1 inhibitor that also affects PCTAIRE-3. It disrupts CDK-dependent phosphorylation, leading to cell cycle arrest. | ||||||
NU6102 | 444722-95-6 | sc-222082 sc-222082A | 1 mg 5 mg | $55.00 $122.00 | 3 | |
NU6102 is an ATP-competitive inhibitor of CDK2 and CDK1, including PCTAIRE-3. It inhibits kinase activity, interfering with cell cycle progression. | ||||||
Cdk9 Inhibitor II | 140651-18-9 | sc-203326 | 5 mg | $172.00 | 1 | |
CDK9 Inhibitor II primarily targets CDK9 but also affects CDK2, CDK1, and PCTAIRE-3. It interferes with kinase activity, leading to cell cycle arrest. | ||||||
PHA 767491 hydrochloride | 942425-68-5 | sc-204187 sc-204187A | 10 mg 50 mg | $194.00 $786.00 | 3 | |
PHA-767491 is a selective CDK inhibitor that targets CDK2 and CDK1, including PCTAIRE-3. It inhibits kinase activity, causing cell cycle arrest. | ||||||