Lipid Biosynthesis Inhibitors
Items 11 to 14 of 14 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
URB-754 | 86672-58-4 | sc-200671 sc-200671A | 10 mg 50 mg | $80.00 $240.00 | ||
URB-754 is an influential compound in lipid biosynthesis, primarily functioning as a selective modulator of diacylglycerol acyltransferase (DGAT). By binding to the enzyme's active site, it alters substrate affinity and enzymatic efficiency, thereby impacting triglyceride synthesis. Its unique hydrophobic interactions enhance membrane fluidity, while its ability to form transient complexes with lipid intermediates can redirect metabolic flux, ultimately influencing cellular lipid homeostasis. | ||||||
Difluoro Atorvastatin | 693794-20-6 | sc-394113 | 5 mg | $360.00 | ||
Difluoro Atorvastatin plays a pivotal role in lipid biosynthesis by selectively inhibiting HMG-CoA reductase, a key enzyme in the mevalonate pathway. Its unique fluorinated structure enhances binding affinity, promoting a conformational change that stabilizes the enzyme-substrate complex. This alteration in reaction kinetics effectively reduces cholesterol synthesis. Additionally, its lipophilic nature facilitates integration into lipid membranes, influencing membrane dynamics and cellular signaling pathways. | ||||||
Triacsin C, lyophilized | 76896-80-5 | sc-477680 sc-477680A | 200 µg 1 mg | $408.00 $1362.00 | 3 | |
Triacsin C is a potent inhibitor of acyl-CoA synthetase, disrupting lipid biosynthesis by preventing the activation of fatty acids. Its unique structure allows for specific interactions with the enzyme's active site, leading to altered substrate availability and metabolic flux. This inhibition affects various lipid metabolic pathways, influencing the synthesis of complex lipids. The compound's stability in lyophilized form enhances its utility in biochemical studies, providing insights into lipid metabolism regulation. | ||||||
N-[3,5-Bis(decyloxy)phenyl]-N-(carboxymethyl)glycine | 153125-17-8 | sc-507222 | 25 mg | $1310.00 | ||
N-[3,5-Bis(decyloxy)phenyl]-N-(carboxymethyl)glycine plays a significant role in lipid biosynthesis by modulating lipid metabolism pathways. Its unique molecular structure facilitates interactions with key enzymes involved in fatty acid synthesis, enhancing reaction kinetics. The compound's hydrophobic decyloxy groups promote membrane integration, influencing lipid bilayer dynamics and stability. This interaction can lead to altered lipid profiles, impacting cellular functions and signaling pathways. | ||||||