Items 1 to 10 of 401 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Cholesterol | 57-88-5 | sc-202539C sc-202539E sc-202539A sc-202539B sc-202539D sc-202539 | 5 g 5 kg 100 g 250 g 1 kg 25 g | $26.00 $2754.00 $126.00 $206.00 $572.00 $86.00 | 11 | |
Cholesterol is a vital lipid that plays a crucial role in maintaining cellular membrane integrity and fluidity. Its unique amphipathic structure allows it to interact with phospholipids, stabilizing membrane architecture. Cholesterol also serves as a precursor for steroid hormones, influencing various biosynthetic pathways. Its ability to form lipid rafts enhances protein interactions and signaling, impacting cellular communication and transport mechanisms within membranes. | ||||||
7-Dehydrocholesterol | 434-16-2 | sc-214398 sc-214398A sc-214398B sc-214398C sc-214398D | 1 g 5 g 10 g 25 g 50 g | $27.00 $56.00 $146.00 $218.00 $454.00 | 4 | |
7-Dehydrocholesterol is a crucial sterol in the biosynthetic pathway of cholesterol, serving as a precursor in the synthesis of vitamin D. Its unique double bond configuration allows for specific interactions with enzymes involved in lipid metabolism, influencing the fluidity and permeability of cellular membranes. This compound also participates in photochemical reactions under UV light, leading to the formation of biologically active metabolites, which can modulate various cellular processes. | ||||||
Atorvastatin calcium salt trihydrate | 344423-98-9 | sc-364723 sc-364723A sc-364723B | 10 mg 25 mg 100 mg | $140.00 $390.00 $635.00 | ||
Atorvastatin calcium salt trihydrate exhibits unique properties as a lipid-modulating agent, characterized by its ability to inhibit HMG-CoA reductase, a key enzyme in the cholesterol biosynthesis pathway. This compound interacts with specific binding sites, altering enzyme kinetics and reducing cholesterol synthesis. Its hydrophilic and lipophilic balance facilitates effective solubility in biological systems, enhancing its distribution and interaction with lipid membranes, thereby influencing lipid metabolism and homeostasis. | ||||||
Lithocholic acid 3-sulfate disodium salt | 64936-81-8 | sc-215263 sc-215263A | 50 mg 750 mg | $156.00 $2040.00 | 5 | |
Lithocholic acid 3-sulfate disodium salt is a bile acid derivative that plays a significant role in lipid metabolism. Its sulfate group enhances solubility in aqueous environments, facilitating interactions with lipid bilayers. This compound can modulate membrane properties, influencing lipid organization and fluidity. Additionally, it participates in the formation of micelles, aiding in the transport and absorption of lipids, while also impacting cellular signaling pathways through its interactions with membrane receptors. | ||||||
Digitonin | 11024-24-1 | sc-280675A sc-280675 sc-280675B sc-280675C sc-280675D sc-280675E | 100 mg 250 mg 1 g 2.5 g 5 g 10 g | $82.00 $160.00 $375.00 $780.00 $1450.00 $2675.00 | 10 | |
Digitonin is a glycoside derived from the plant Digitalis, known for its ability to selectively interact with cholesterol in lipid membranes. This interaction disrupts membrane integrity, facilitating the solubilization of membrane proteins. Digitonin's unique structure allows it to form stable complexes with cholesterol, influencing membrane fluidity and permeability. Its distinct binding properties enable it to act as a powerful tool in studying membrane dynamics and protein interactions. | ||||||
Dehydroergosterol | 516-85-8 | sc-214967 sc-214967A | 5 mg 50 mg | $136.00 $610.00 | 1 | |
Dehydroergosterol is a sterol derivative that plays a crucial role in membrane fluidity and stability due to its unique planar structure, which facilitates tight packing within lipid bilayers. This compound exhibits distinct hydrophobic interactions, influencing the permeability of membranes. Its presence can modulate the activity of membrane proteins and impact signaling pathways, contributing to cellular homeostasis. Additionally, dehydroergosterol's photochemical properties allow it to participate in light-driven reactions, enhancing its role in various biochemical processes. | ||||||
Micafungin | 235114-32-6 | sc-391640 | 1 mg | $286.00 | ||
Micafungin is a cyclic lipopeptide that exhibits unique interactions with fungal cell membranes. Its lipid component enhances membrane permeability, allowing for specific binding to glucan synthase, which disrupts cell wall integrity. This compound's amphiphilic nature promotes self-assembly into micelle-like structures, influencing lipid bilayer dynamics. Furthermore, its distinct molecular conformation facilitates selective interactions with membrane proteins, potentially altering cellular signaling cascades. | ||||||
Sesame oil | 8008-74-0 | sc-215848 sc-215848A | 250 ml 1 L | $50.00 $130.00 | 5 | |
Sesame oil is a triglyceride-rich lipid characterized by its high content of unsaturated fatty acids, particularly oleic and linoleic acids. Its unique molecular structure allows for effective emulsification, enhancing the stability of oil-water mixtures. The oil's antioxidant properties stem from its lignan content, which can scavenge free radicals. Additionally, sesame oil exhibits low viscosity, promoting fluidity and enhancing its ability to interact with various biological membranes, influencing lipid metabolism pathways. | ||||||
Triethylene glycol monooctyl ether | 19327-38-9 | sc-253750 | 1 ml | $125.00 | ||
Triethylene glycol monooctyl ether is a versatile lipid that showcases remarkable amphiphilic properties, enabling it to interact favorably with both hydrophilic and hydrophobic environments. Its ether linkages enhance solubility in various solvents, while the octyl chain contributes to its ability to form micelles and emulsions. This compound can influence surface tension and stabilize colloidal systems, facilitating unique molecular interactions that affect aggregation behavior and phase behavior in complex mixtures. | ||||||
rac-1,2-Distearoyl-3-chloropropanediol-d5 | 1246818-85-8 | sc-497253 | 2.5 mg | $273.00 | ||
Rac-1,2-Distearoyl-3-chloropropanediol-d5 is a lipid characterized by its unique amphiphilic nature, which promotes the formation of stable micelles and lipid bilayers. The presence of the chloropropanediol moiety introduces specific steric effects that influence molecular packing and phase behavior. This compound exhibits distinct interactions with water and other lipids, affecting membrane dynamics and fluidity. Its isotopic labeling allows for advanced tracking in metabolic studies, providing insights into lipid metabolism and cellular interactions. |