Date published: 2025-12-7

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DGAT Inhibitors

Santa Cruz Biotechnology now offers a broad range of DGAT Inhibitors for use in various applications. Diacylglycerol O-acyltransferase (DGAT) enzymes are key players in lipid metabolism, catalyzing the final step in triglyceride synthesis by converting diacylglycerol (DAG) and fatty acyl-CoA into triglycerides. DGAT Inhibitors are crucial tools in scientific research, allowing researchers to explore the regulation of triglyceride biosynthesis and its impact on cellular lipid storage, energy balance, and metabolic health. By inhibiting DGAT activity, scientists can investigate how disruptions in triglyceride synthesis affect lipid accumulation, adipocyte function, and overall metabolic processes, providing insights into the enzyme's role in conditions such as obesity, fatty liver disease, and insulin resistance. These inhibitors are widely used in studies aimed at understanding the molecular mechanisms of lipid metabolism, as well as in exploring the broader implications of altered triglyceride synthesis on cellular energy homeostasis. Additionally, DGAT Inhibitors are valuable in research focusing on the interplay between lipid metabolism and signaling pathways that regulate various physiological functions, including inflammation and glucose metabolism. The availability of these inhibitors has significantly advanced research in fields such as biochemistry, molecular biology, and metabolic studies, offering essential tools for dissecting the complex networks that control lipid synthesis and storage. View detailed information on our available DGAT Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Amidepsine A

169181-28-6sc-221244
sc-221244A
1 mg
2.5 mg
$257.00
$497.00
(1)

Amidepsine A functions as a potent diacylglycerol acyltransferase (DGAT) inhibitor, characterized by its ability to modulate lipid metabolism. Its unique molecular structure facilitates specific interactions with the enzyme's active site, altering substrate binding dynamics. The compound exhibits distinctive reaction kinetics, demonstrating a competitive inhibition profile that influences triglyceride synthesis pathways. This modulation can lead to significant alterations in lipid droplet formation and cellular energy homeostasis.

Xanthohumol from hop (Humulus lupulus)

6754-58-1sc-301982
5 mg
$354.00
1
(0)

Xanthohumol, derived from hops, acts as a diacylglycerol acyltransferase (DGAT) modulator, showcasing unique interactions with lipid metabolic pathways. Its structure allows for selective binding to DGAT, influencing enzyme conformation and substrate accessibility. This compound exhibits non-competitive inhibition, impacting triglyceride synthesis rates and altering lipid droplet dynamics. Additionally, Xanthohumol's hydrophobic properties enhance its interaction with membrane-associated enzymes, further influencing lipid metabolism.

Cochlioquinone A

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

Cochlioquinone A functions as a diacylglycerol acyltransferase (DGAT) with distinctive molecular characteristics that facilitate its role in lipid metabolism. Its unique structural features enable it to engage in specific hydrogen bonding and hydrophobic interactions with the enzyme's active site, modulating catalytic efficiency. This compound exhibits a substrate-dependent kinetic profile, influencing the rate of triglyceride formation and altering lipid droplet morphology through its dynamic interactions with cellular membranes.

Cochlioquinone B

32450-26-3sc-202110
500 µg
$246.00
(0)

Cochlioquinone B acts as a diacylglycerol acyltransferase (DGAT), showcasing unique binding affinities that enhance its catalytic role in lipid biosynthesis. Its structural conformation allows for selective interactions with acyl-CoA substrates, promoting efficient esterification processes. The compound's distinct hydrophobic regions contribute to its ability to stabilize lipid bilayers, influencing membrane fluidity and integrity, while its reaction kinetics reveal a complex interplay with various lipid species, impacting overall metabolic pathways.

Amidepsine D

79786-34-8sc-221245
sc-221245A
1 mg
2.5 mg
$267.00
$543.00
(0)

Amidepsine D functions as a diacylglycerol acyltransferase (DGAT), exhibiting remarkable specificity in substrate recognition that facilitates lipid assembly. Its unique molecular architecture enables effective interactions with both diacylglycerol and acyl-CoA, driving rapid acylation reactions. The compound's hydrophilic and hydrophobic domains create a dynamic environment that modulates enzyme activity, influencing lipid droplet formation and cellular energy storage pathways.

A 922500

959122-11-3sc-203793
10 mg
$265.00
2
(1)

A 922500 acts as a diacylglycerol acyltransferase (DGAT), characterized by its intricate binding dynamics with lipid substrates. Its structural features promote selective acylation, enhancing the efficiency of lipid synthesis. The compound's unique conformational flexibility allows it to adapt during catalysis, optimizing reaction kinetics. Additionally, its amphipathic nature influences membrane interactions, playing a crucial role in lipid droplet biogenesis and metabolic regulation.