Date published: 2026-4-9

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Cdk10 Inhibitors

CDK10 inhibitors belong to a class of chemical compounds specifically designed to target and modulate the activity of Cyclin-Dependent Kinase 10 (CDK10). CDK10 is a member of the cyclin-dependent kinase family, which plays a pivotal role in governing cell cycle progression and regulation. These inhibitors are meticulously crafted to interact with the active site of CDK10, exerting their inhibitory effect by disrupting the kinase's ability to phosphorylate its target substrates. By interfering with this phosphorylation activity, CDK10 inhibitors influence the intricate network of molecular events that control cell division, making them potential candidates for research into cellular mechanisms and their implications in various biological contexts. CDK10 inhibitors primarily fall into the category of small molecules. These compounds are designed with a specific molecular structure that allows them to effectively bind to the active site of CDK10, often competing with adenosine triphosphate (ATP) for binding. Through this interaction, they hinder the phosphorylation process catalyzed by CDK10, thereby influencing downstream signaling pathways related to cell cycle progression. This class of inhibitors has garnered interest due to its potential in unveiling the role of CDK10 in cellular processes and exploring the broader implications of its activity in different biological systems. In conclusion, CDK10 inhibitors represent a specialized class of small molecules designed to target CDK10's enzymatic activity and influence cell cycle regulation. By disrupting the kinase's phosphorylation activity, these inhibitors provide valuable insights into the intricate web of molecular events governing cell division and hold promise for furthering our understanding of cellular processes in diverse contexts.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$259.00
41
(3)

Flavopiridol functions as a potent inhibitor of cyclin-dependent kinase 10 (Cdk10) through its unique ability to stabilize the inactive conformation of the enzyme. By selectively binding to the ATP-binding site, it alters the enzyme's structural dynamics, effectively hindering substrate access. This interaction not only impacts phosphorylation rates but also influences downstream signaling pathways, showcasing its role in modulating cellular processes with high specificity.

Roscovitine

186692-46-6sc-24002
sc-24002A
1 mg
5 mg
$94.00
$265.00
42
(2)

An ATP-competitive CDK inhibitor that affects various CDKs, including CDKIt disrupts the cell cycle by inhibiting CDKs involved in regulating cell division.

Alsterpaullone

237430-03-4sc-202453
sc-202453A
1 mg
5 mg
$68.00
$312.00
2
(1)

A synthetic compound with inhibitory effects on several CDKs, including CDKIt interferes with CDK-mediated phosphorylation events, impacting cell cycle progression.

P276-00

920113-03-7sc-477932
1 mg
$380.00
(0)

A small molecule CDK inhibitor that shows potential against CDK10 and other CDKs. It aims to disrupt the cell cycle by targeting multiple CDK-regulated points.

NU2058

161058-83-9sc-202744
sc-202744A
5 mg
25 mg
$66.00
$321.00
2
(1)

An ATP-competitive inhibitor that targets multiple CDKs, including CDKResearch explores its ability to influence cell cycle progression and inhibit CDK-mediated phosphorylation.