DGAT

Diacylglycerol acyltransferase (DGAT) inhibitors block the final step of triglyceride synthesis. DGAT enzymes transfer a fatty acyl group from acyl-coenzyme A (acyl-CoA) onto diacylglycerol. DGAT1 was identified in 1998 through its sequence similarity to cholesterol acyltransferases. DGAT2, cloned in 2001, shares no sequence similarity with DGAT1 and belongs to a separate gene family. Both enzymes are studied in models of dietary fat absorption, hepatic lipid storage and obesity. A 922500, PF-04620110, AZD7687 and pradigastat are DGAT1 inhibitors, whereas PF-06424439 inhibits DGAT2. Comparing the two classes helps separate the roles of the isoforms in intestine, liver and adipose tissue.

Items 26-35 of 35

  • IONIS-DGAT 2Rx
    Cat. No.
    A69263

    IONIS-DGAT 2Rx

    Synonyms: ISIS 484137; ION-224

    IONIS-DGAT 2Rx (ION-224) is a selective inhibitor of diacylglycerol O-acyltransferase 2 (DGAT2), an enzyme involved in triglyceride synthesis and lipid metabolism. This compound has demonstrated potential in research focused on atherosclerosis and related metabolic disorders. Its ability to modulate lipid accumulation makes it a valuable tool for investigating the pathophysiology of vascular diseases and the development of novel therapeutic strategies.

    Out of stock

    All 3 sizes
  • Ent-Calquiquelignan E
    Cat. No.
    A69265

    Ent-Calquiquelignan E

    Ent-Calquiquelignan E is a selective inhibitor of diacylglycerol acyltransferase 1 (DGAT1), demonstrating an IC50 of 71.5 μM. This flavonoid lignan compound is valuable for studies investigating metabolic disorders and related pathways. Its inhibitory action on DGAT1 may provide insights into lipid metabolism and potential therapeutic approaches for metabolic diseases.

    Out of stock

    All 3 sizes
  • DGAT-1 inhibitor 3
    Cat. No.
    A69272

    DGAT-1 inhibitor 3

    DGAT-1 Inhibitor 3 is a selective inhibitor of diacylglycerol O-acyltransferase 1 (DGAT-1), exhibiting a potent inhibitory effect with an IC50 value of 0.038 µM. This compound is relevant for studies investigating lipid metabolism and has significant potential in obesity and diabetes research. Its activity can facilitate the understanding of DGAT-1's role in metabolic disorders and aid in the development of therapeutic strategies for associated diseases.

    5 mg
    $215.00
    10 mg
    $355.00
    All 4 sizes
  • JNJ-DGAT1-A
    Cat. No.
    A69274

    JNJ-DGAT1-A

    JNJ-DGAT1-A is a selective inhibitor of diacylglycerol acyltransferase 1 (DGAT1), which plays a critical role in triglyceride (TG) synthesis. By inhibiting DGAT1 activity, JNJ-DGAT1-A reduces the accumulation of triglycerides, making it a valuable tool for research into lipid metabolism and related disorders. This compound is utilized in studies aimed at understanding obesity, diabetes, and other metabolic diseases.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Roselipin 2B
    Cat. No.
    A69284

    Roselipin 2B

    Roselipin 2B is a selective inhibitor of diacylglycerol acyltransferases (DGAT), which play a critical role in lipid metabolism. It effectively suppresses DGAT activity in rat hepatic microcosms, making it a valuable tool for studying lipid synthesis and storage pathways. This compound can be utilized in research focused on metabolic disorders, obesity, and related metabolic diseases.

    Out of stock

    All 3 sizes
  • Roselipin 1A
    Cat. No.
    A69288

    Roselipin 1A

    Roselipin 1A is a selective diacylglycerol acyltransferase (DGAT) inhibitor. This compound demonstrates significant inhibition of DGAT activity in rat hepatic microcosm, which is critical for triglyceride synthesis and lipid metabolism. Roselipin 1A is applicable in studies investigating lipid homeostasis, obesity, and associated metabolic disorders.

    Out of stock

    All 3 sizes
  • Roselipin 1B
    Cat. No.
    A69290

    Roselipin 1B

    Roselipin 1B is an inhibitor of diacylglycerol acyltransferases (DGAT), which play a critical role in lipid metabolism. This compound effectively disrupts DGAT activity in rat hepatic microcosm, making it a valuable tool for studying lipid biosynthesis and related metabolic pathways. Its application is significant in research focused on obesity, metabolic disorders, and potential therapeutic strategies targeting lipid accumulation.

    Out of stock

    All 3 sizes
  • Roselipin 2A
    Cat. No.
    A69292

    Roselipin 2A

    Roselipin 2A is a specific inhibitor of diacylglycerol acyltransferases (DGAT), targeting the enzymatic activity involved in triglyceride synthesis. This compound has demonstrated efficacy in disrupting lipid metabolism in rat hepatic microcosm studies. It is valuable for research exploring metabolic pathways and potential therapeutic strategies for metabolic disorders.

    Out of stock

    All 3 sizes
  • Amidepsin B
    Cat. No.
    A69293

    Amidepsin B

    Amidepsin B is a diacylglycerol acyltransferase (DGAT) inhibitor that plays a crucial role in lipid metabolism. By inhibiting DGAT, Amidepsin B effectively lowers triglyceride synthesis and can modulate metabolic pathways associated with obesity and insulin resistance. This compound is valuable for research in metabolic disorders, providing insights into lipid homeostasis and potential therapeutic strategies for metabolic diseases.

    Out of stock

    All 3 sizes
  • Amidepsin C
    Cat. No.
    A69294

    Amidepsin C

    Amidepsin C is a selective inhibitor of diacylglycerol acyltransferase (DGAT), a key enzyme involved in triglyceride synthesis. By inhibiting DGAT, Amidepsin C plays a crucial role in reducing lipogenesis and may influence metabolic regulation. This compound has potential applications in research related to obesity, diabetes, and lipid metabolism.

    Out of stock

    All 3 sizes

Items 26-35 of 35

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