Items 191 to 200 of 401 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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1,2-Distearoyl-sn-glycero-3-phosphate, sodium salt | 108321-18-2 | sc-208744 sc-208744A | 100 mg 250 mg | $76.00 $114.00 | ||
1,2-Distearoyl-sn-glycero-3-phosphate, sodium salt is a phospholipid characterized by its dual stearoyl chains and phosphate group, which facilitates strong interactions with membrane proteins and other lipids. Its amphiphilic nature promotes the formation of bilayers, enhancing membrane integrity and fluidity. This compound plays a crucial role in modulating membrane dynamics and can influence the behavior of membrane-associated enzymes and receptors, impacting cellular signaling pathways. | ||||||
Behenyl oleate | 127566-70-5 | sc-214578 | 50 mg | $210.00 | ||
Behenyl oleate is a long-chain fatty acid ester that exhibits unique properties due to its hydrophobic tail and polar head group. This amphiphilic structure allows it to form stable micelles and lipid bilayers, enhancing solubilization of hydrophobic compounds. Its interactions with other lipids can influence phase behavior and viscosity, while its ability to undergo hydrolysis can affect lipid metabolism pathways. Additionally, its low toxicity and biodegradability make it an interesting candidate for various applications in lipid chemistry. | ||||||
1-Hexadecyl Lysophosphatidic Acid (sodium salt) | sc-220468 sc-220468A | 500 µg 1 mg | $21.00 $40.00 | |||
1-Hexadecyl Lysophosphatidic Acid (sodium salt) is a unique amphiphilic lipid characterized by its long hydrophobic alkyl chain and a polar phosphate head. This structure facilitates the formation of lipid aggregates, influencing membrane fluidity and permeability. Its distinct molecular interactions can modulate signaling pathways and cellular responses. The compound's ability to participate in self-assembly processes and its stability in aqueous environments highlight its significance in lipid biochemistry. | ||||||
Azelaoyl-PAF | 354583-69-0 | sc-221278 sc-221278A | 1 mg 5 mg | $200.00 $440.00 | ||
Azelaoyl-PAF is a unique lipid that features a distinctive acyl chain, contributing to its amphiphilic nature. This compound exhibits remarkable interfacial activity, promoting the formation of stable emulsions and influencing lipid bilayer organization. Its ability to participate in specific van der Waals interactions enhances membrane integrity and alters permeability. Additionally, Azelaoyl-PAF can modulate lipid raft dynamics, impacting cellular signaling pathways and membrane fluidity. | ||||||
Butanoyl PAF | sc-221386 sc-221386A | 1 mg 5 mg | $46.00 $205.00 | 1 | ||
Butanoyl PAF is a notable lipid characterized by its short acyl chain, which imparts unique fluidity and flexibility to lipid membranes. This compound engages in specific hydrophobic interactions, facilitating the formation of lipid aggregates and influencing membrane curvature. Its reactivity as an acid halide allows for the formation of diverse derivatives, potentially altering lipid metabolism. Butanoyl PAF also plays a role in modulating membrane protein interactions, affecting cellular communication. | ||||||
DMTAP mesylate | sc-221560 sc-221560A | 5 mg 25 mg | $200.00 $400.00 | |||
DMTAP mesylate is a distinctive lipid that features a quaternary ammonium structure, enhancing its amphiphilic properties. This compound exhibits strong electrostatic interactions with negatively charged lipid bilayers, promoting membrane stability and influencing lipid packing. Its unique reactivity as an acid halide enables the formation of various lipid derivatives, which can modulate membrane dynamics and alter cellular signaling pathways. Additionally, DMTAP mesylate can impact membrane permeability, affecting ion transport. | ||||||
Δ2-trans Eicosenoic Acid | 2127095-72-9 | sc-221740 sc-221740A | 5 mg 10 mg | $49.00 $93.00 | ||
Δ2-trans Eicosenoic Acid is a unique unsaturated fatty acid characterized by its cis double bond configuration, which influences its fluidity and packing within lipid membranes. This structural feature enhances its ability to integrate into phospholipid bilayers, affecting membrane curvature and flexibility. Its distinct reactivity allows for the formation of bioactive lipid mediators, which can modulate cellular signaling and metabolic pathways, contributing to diverse physiological processes. | ||||||
N-butyryl-L-Homoserine lactone-d5 | sc-221996 sc-221996A | 250 µg 1 mg | $25.00 $48.00 | |||
N-butyryl-L-Homoserine lactone-d5 is a signaling molecule that plays a crucial role in quorum sensing among bacteria. Its unique structure allows for specific interactions with receptor proteins, influencing gene expression and biofilm formation. The deuterated form enhances tracking in metabolic studies, providing insights into lipid metabolism and cellular communication. Its behavior as an acyl homoserine lactone facilitates the modulation of various biochemical pathways, impacting microbial community dynamics. | ||||||
N-hexanoyl-L-Homoserine lactone-d3 | sc-222006 sc-222006A | 1 mg 5 mg | $64.00 $270.00 | 1 | ||
N-hexanoyl-L-Homoserine lactone-d3 is a versatile lipid that serves as a key player in intercellular signaling, particularly in bacterial communication. Its distinct acyl chain length influences membrane fluidity and permeability, affecting how it interacts with lipid bilayers. The deuterated variant allows for precise monitoring in studies of lipid dynamics, revealing insights into metabolic pathways and the regulation of gene expression. This compound's unique properties facilitate complex biochemical interactions, shaping microbial behavior and community structure. | ||||||
13S-Hydroxy-9Z,11E-octadecadiene-(2-biotinyl)hydrazide | sc-297972 | 100 µg | $235.00 | |||
13S-Hydroxy-9Z,11E-octadecadiene-(2-biotinyl)hydrazide is a specialized lipid that exhibits unique molecular interactions due to its biotinylated structure, enhancing affinity for biotin-binding proteins. This compound participates in lipid metabolism and cellular signaling pathways, influencing membrane organization and dynamics. Its hydrazide functionality allows for specific conjugation reactions, facilitating the study of lipid-protein interactions and cellular processes, thereby providing insights into lipid behavior in biological systems. |