Date published: 2025-12-8

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DGK Inhibitors

Santa Cruz Biotechnology now offers a broad range of DGK Inhibitors for use in various applications. Diacylglycerol kinases (DGKs) are a family of enzymes that play a pivotal role in cellular signaling by converting diacylglycerol (DAG) into phosphatidic acid (PA), thereby regulating the balance between these two important lipid signaling molecules. DGK Inhibitors are essential tools in scientific research, enabling the exploration of DGK's role in various signaling pathways that influence cell growth, differentiation, and apoptosis. By inhibiting DGK activity, researchers can study how disruptions in DAG and PA signaling impact cellular processes, offering insights into the enzyme's involvement in immune responses, cancer progression, and metabolic regulation. These inhibitors are widely used in biochemical and cell-based assays to understand the specific functions of different DGK isoforms and their regulatory mechanisms within distinct cellular contexts. Additionally, DGK Inhibitors are valuable for investigating the interplay between lipid signaling and other molecular pathways that control critical physiological functions. The availability of these inhibitors has significantly advanced research in fields such as molecular biology and biochemistry, providing researchers with powerful tools to dissect the complex networks that govern lipid signaling and its broader implications in health and disease. View detailed information on our available DGK Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Calphostin C

121263-19-2sc-3545
sc-3545A
100 µg
1 mg
$336.00
$1642.00
20
(1)

Calphostin C functions as a diacylglycerol kinase (DGK), exhibiting a remarkable affinity for diacylglycerol substrates. Its unique binding site facilitates specific phosphorylation, modulating lipid signaling pathways. The compound's stereochemistry contributes to its selectivity, influencing downstream cellular responses. Furthermore, Calphostin C's ability to alter membrane fluidity enhances its interaction with various lipid environments, impacting cellular signaling cascades and metabolic processes.

R 59-022

93076-89-2sc-203227
5 mg
$122.00
1
(1)

R 59-022 acts as a diacylglycerol kinase (DGK) with a distinctive mechanism of action, characterized by its rapid kinetics in phosphorylating diacylglycerol. Its structural conformation allows for selective interactions with lipid bilayers, promoting unique conformational changes that influence membrane dynamics. Additionally, R 59-022's ability to modulate enzyme activity through competitive inhibition highlights its role in fine-tuning lipid-mediated signaling pathways, impacting cellular homeostasis.

Dioctanoylglycol

627-86-1sc-203567
50 mg
$132.00
(0)

Dioctanoylglycol functions as a diacylglycerol kinase (DGK) with a unique ability to engage in specific lipid interactions, enhancing its affinity for membrane-associated substrates. Its hydrophobic nature facilitates integration into lipid bilayers, where it can influence membrane fluidity and organization. The compound exhibits distinct reaction kinetics, allowing for efficient phosphorylation of diacylglycerol, thereby playing a critical role in regulating lipid signaling cascades and cellular energy balance.

DAG Kinase Inhibitor II

120166-69-0sc-3551
sc-3551A
5 mg
25 mg
$135.00
$380.00
1
(1)

DAG Kinase Inhibitor II acts as a selective modulator of diacylglycerol kinase activity, exhibiting a unique capacity to disrupt lipid-mediated signaling pathways. Its structural conformation allows for specific binding interactions with the enzyme's active site, effectively altering substrate accessibility. This compound demonstrates notable selectivity in inhibiting DGK isoforms, influencing downstream signaling events and cellular responses through its kinetic profile and interaction dynamics.

Cochlioquinone A

32450-25-2sc-202109
500 µg
$291.00
1
(1)

Cochlioquinone A functions as a diacylglycerol kinase (DGK) modulator, characterized by its ability to engage in specific molecular interactions that influence lipid metabolism. Its unique structural features facilitate selective binding to DGK isoforms, impacting the enzyme's catalytic efficiency. The compound's kinetic behavior reveals a distinct inhibition pattern, altering the dynamics of lipid signaling pathways and contributing to the regulation of cellular processes through its interaction with membrane-associated lipids.