Items 221 to 230 of 401 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Triarachidin | 620-64-4 | sc-296599 sc-296599A | 1 g 5 g | $128.00 $520.00 | ||
Triarachidin is a long-chain fatty acid that exhibits remarkable structural characteristics, primarily due to its extensive hydrocarbon chain. This configuration allows it to interact favorably with lipid bilayers, enhancing membrane stability and influencing phase behavior. Its unique ability to form van der Waals interactions contributes to the packing density of lipid assemblies, while its hydrophobic nature facilitates the formation of lipid rafts, impacting cellular signaling pathways. | ||||||
Palmitic anhydride | 623-65-4 | sc-215665 | 1 g | $41.00 | ||
Palmitic anhydride, as a lipid, showcases unique reactivity due to its anhydride functional group, which can readily participate in acylation reactions. This property allows it to form esters with alcohols, influencing lipid metabolism and synthesis pathways. Its hydrophobic characteristics promote aggregation in nonpolar environments, enhancing its role in lipid bilayer formation. Additionally, its ability to undergo hydrolysis can impact lipid turnover and cellular energy dynamics. | ||||||
1,2-Dilaurin | 17598-94-6 | sc-506205 | 50 mg | $219.00 | ||
1,2-Dilaurin is a diacylglycerol that exhibits unique lipid properties due to its long-chain fatty acid composition. Its hydrophobic nature promotes self-assembly into micelles and lipid bilayers, influencing membrane fluidity and stability. The compound's ability to form hydrogen bonds with water molecules enhances its emulsifying properties. Additionally, its distinct fatty acid chains can engage in van der Waals interactions, affecting its phase behavior and interactions with other lipids. | ||||||
Methyl valerate | 624-24-8 | sc-215377 | 1 ml | $35.00 | ||
Methyl valerate, as a lipid, exhibits distinctive properties due to its ester functional group, which facilitates interactions with various biomolecules. Its moderate polarity allows it to integrate into lipid membranes, influencing fluidity and permeability. The compound can engage in transesterification reactions, altering lipid profiles and impacting metabolic pathways. Furthermore, its volatility and low viscosity contribute to its behavior in lipid mixtures, affecting phase transitions and molecular organization. | ||||||
D-myo-Inositol-1,2,3,6-tetraphosphate, sodium salt | sc-223914 sc-223914A | 100 µg 500 µg | $165.00 $744.00 | |||
D-myo-Inositol-1,2,3,6-tetraphosphate, sodium salt, is a phosphoinositide that plays a crucial role in cellular signaling and lipid metabolism. Its unique structure allows for specific interactions with proteins and enzymes, influencing pathways such as calcium signaling and phospholipid turnover. The presence of multiple phosphate groups enhances its solubility in aqueous environments, facilitating its participation in cellular processes. This compound also exhibits distinct reactivity, participating in phosphorylation and dephosphorylation reactions that modulate various biological functions. | ||||||
3-Deoxy-3-fluoro-D-myo-inositol 1,4,5-trisphosphate . hexasodium salt | 129365-68-0 | sc-506412 | 100 µg | $200.00 | ||
3-Deoxy-3-fluoro-D-myo-inositol 1,4,5-trisphosphate hexasodium salt is a unique lipid derivative that plays a pivotal role in cellular signaling pathways. Its fluorinated structure enhances binding affinity to specific receptors, influencing phosphoinositide metabolism. This compound exhibits distinct reaction kinetics, facilitating rapid intracellular calcium release and modulating various signaling cascades. Its solubility in aqueous environments allows for effective interaction with membrane proteins, impacting cellular responses. | ||||||
Ethyl undecanoate | 627-90-7 | sc-215000 | 25 g | $45.00 | ||
Ethyl undecanoate, a lipid, showcases unique characteristics stemming from its long hydrocarbon chain and ester linkage. This structure enhances its hydrophobic interactions, promoting solubility in nonpolar environments. The compound participates in enzymatic reactions, such as lipolysis, influencing fatty acid release and energy metabolism. Its ability to form micelles and emulsions plays a crucial role in lipid transport and storage, impacting cellular energy dynamics and membrane integrity. | ||||||
D-myo-Inositol-2,3,5,6-tetraphosphate, sodium salt | sc-223931 sc-223931A | 100 µg 500 µg | $57.00 $339.00 | |||
D-myo-Inositol-2,3,5,6-tetraphosphate, sodium salt, is a phosphoinositide derivative that plays a crucial role in cellular signaling pathways. Its unique structure allows for specific interactions with proteins, influencing signal transduction and cellular responses. The compound's high affinity for calcium ions can modulate intracellular calcium levels, impacting various physiological processes. Additionally, its ability to form complexes with other lipids enhances membrane organization and functionality, contributing to cellular homeostasis. | ||||||
Pentadecyl acetate | 629-58-3 | sc-215688 sc-215688A | 100 mg 500 mg | $47.00 $142.00 | ||
Pentadecyl acetate, a lipid, features a lengthy hydrocarbon tail that contributes to its distinctive amphiphilic nature. This structure facilitates the formation of lipid bilayers and micelles, enhancing its role in membrane dynamics. The compound exhibits unique phase behavior, influencing its interactions with other lipids and proteins. Its ester functional group allows for specific enzymatic hydrolysis, impacting lipid metabolism pathways and contributing to cellular signaling processes. | ||||||
2-Oleoylglycerol | 3443-84-3 | sc-213888 sc-213888B sc-213888A | 1 mg 5 mg 10 mg | $52.00 $173.00 $316.00 | 2 | |
2-Oleoylglycerol is a monoacylglycerol that serves as a key lipid mediator in various biological processes. Its unsaturated fatty acid chain allows for fluidity in membrane structures, facilitating lipid-protein interactions. This compound can influence the activity of enzymes and receptors, modulating metabolic pathways. Additionally, its unique hydrophobic properties enable it to participate in micelle formation, enhancing the solubility of other lipophilic substances in biological systems. |