Date published: 2025-10-25

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PCTAIRE-3 Inhibitors

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.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

RO-3306

872573-93-8sc-358700
sc-358700A
sc-358700B
1 mg
5 mg
25 mg
$65.00
$160.00
$320.00
37
(1)

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

602306-29-6sc-361115
sc-361115A
10 mg
50 mg
$205.00
$865.00
(0)

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

160807-49-8sc-202660
sc-202660A
sc-202660B
1 mg
5 mg
50 mg
$77.00
$315.00
$658.00
1
(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

345627-80-7sc-364621
sc-364621A
5 mg
10 mg
$169.00
$262.00
(1)

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

221243-82-9sc-203765
sc-203765A
10 mg
50 mg
$230.00
$964.00
3
(1)

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

377090-84-1sc-222330
sc-222330A
5 mg
25 mg
$122.00
$383.00
3
(1)

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

660868-91-7sc-203202
500 µg
$107.00
1
(0)

GW843682X is a potent CDK2 and CDK1 inhibitor that also affects PCTAIRE-3. It disrupts CDK-dependent phosphorylation, leading to cell cycle arrest.

NU6102

444722-95-6sc-222082
sc-222082A
1 mg
5 mg
$55.00
$122.00
3
(1)

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

140651-18-9sc-203326
5 mg
$172.00
1
(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

942425-68-5sc-204187
sc-204187A
10 mg
50 mg
$194.00
$786.00
3
(2)

PHA-767491 is a selective CDK inhibitor that targets CDK2 and CDK1, including PCTAIRE-3. It inhibits kinase activity, causing cell cycle arrest.