Items 341 to 350 of 401 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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L-α-Phosphatidylcholine β-(pyren-1-yl)hexanoyl-γ-palmitoyl | 103625-33-8 | sc-358264 sc-358264A | 100 µg 500 µg | $320.00 $480.00 | ||
L-α-Phosphatidylcholine β-(pyren-1-yl)hexanoyl-©-palmitoyl is a specialized lipid that showcases unique amphiphilic properties, facilitating its integration into lipid bilayers. The pyrene moiety enhances fluorescence, enabling real-time monitoring of membrane dynamics. Its acyl chains promote hydrophobic interactions, influencing membrane curvature and stability. This compound's ability to form micelles and liposomes underscores its role in modulating lipid organization and cellular signaling pathways. | ||||||
Ricinelaidic acid sodium salt | 108321-51-3 | sc-215813 | 10 mg | $32.00 | ||
Ricinelaidic acid sodium salt is a distinctive lipid characterized by its dual hydrophilic and hydrophobic regions, which enable it to interact effectively with biological membranes. Its unique structure promotes the formation of stable emulsions, enhancing solubility and bioavailability of other compounds. The sodium salt form increases its ionic character, facilitating interactions with proteins and other biomolecules, thereby influencing membrane fluidity and permeability. This compound plays a significant role in lipid bilayer dynamics and cellular interactions. | ||||||
cis-13,16,19-Docosatrienoic acid methyl ester | 108698-01-7 | sc-214733 | 25 mg | $300.00 | ||
Cis-13,16,19-Docosatrienoic acid methyl ester is a notable lipid with a unique unsaturated fatty acid structure that influences its fluidity and flexibility in lipid bilayers. Its specific cis double bonds enhance molecular interactions, promoting the formation of lipid rafts and modulating membrane properties. This compound participates in various metabolic pathways, impacting energy storage and signaling processes. Its methyl ester form also affects its solubility and reactivity, making it a versatile component in lipid chemistry. | ||||||
1-O-Hexadecyl-3-O-methyl-rac-glycerol | 111188-59-1 | sc-220484 | 250 mg | $50.00 | ||
1-O-Hexadecyl-3-O-methyl-rac-glycerol is a distinctive lipid characterized by its long-chain alkyl group, which enhances hydrophobic interactions within lipid membranes. This compound exhibits unique phase behavior, influencing membrane organization and stability. Its methyl ether functionality contributes to altered reactivity and solubility, facilitating specific interactions with proteins and other lipids. Additionally, it plays a role in modulating membrane permeability and fluidity, impacting cellular dynamics. | ||||||
N-Tetracosanoyl-D-sphingosine 1-benzoate | 123446-98-0 | sc-215486 | 1 mg | $91.00 | ||
N-Tetracosanoyl-D-sphingosine 1-benzoate is a complex lipid featuring a long-chain fatty acyl moiety that promotes strong hydrophobic interactions, crucial for membrane integrity. Its benzoate group introduces unique steric effects, influencing molecular packing and phase transitions. This compound exhibits distinct reactivity patterns, particularly in acylation and esterification reactions, which can modulate lipid bilayer properties and affect lipid-protein interactions, thereby impacting cellular signaling pathways. | ||||||
Dihomo-γ-Linolenoyl PAF C-16 | 155575-01-2 | sc-205292 sc-205292A | 1 mg 5 mg | $45.00 $205.00 | ||
Dihomo-γ-Linolenoyl PAF C-16 is a distinctive lipid known for its elongated polyunsaturated fatty acid chain, which contributes to its unique packing properties within lipid membranes. This compound engages in specific hydrophobic interactions, enhancing membrane stability while also promoting fluidity. Its structure allows for effective modulation of lipid raft formation, influencing signaling pathways and cellular responses through altered membrane dynamics and protein interactions. | ||||||
S-2E | 155730-92-0 | sc-215829 sc-215829A | 5 mg 25 mg | $125.00 $422.00 | ||
S-2E is a notable lipid characterized by its unique amphiphilic structure, which facilitates the formation of micelles and lipid bilayers. Its distinct hydrophobic tail enhances interactions with membrane proteins, influencing their conformation and activity. The compound exhibits rapid reaction kinetics, particularly in acylation processes, allowing it to participate in various lipid metabolic pathways. Additionally, S-2E's ability to form stable emulsions contributes to its role in cellular compartmentalization and signaling. | ||||||
L-NASPA | 155915-46-1 | sc-215223 sc-215223A | 1 mg 5 mg | $140.00 $410.00 | ||
L-NASPA is a distinctive lipid known for its unique ability to form stable lipid aggregates due to its specific hydrophobic and hydrophilic regions. This compound engages in selective molecular interactions that enhance membrane fluidity and permeability. Its reactivity as an acid halide allows for efficient acylation reactions, facilitating the incorporation of fatty acids into complex lipid structures. L-NASPA also plays a role in modulating lipid raft dynamics, impacting cellular signaling pathways. | ||||||
15(S)-HETE Ethanolamide | 161744-53-2 | sc-205041 sc-205041A | 25 µg 50 µg | $133.00 $255.00 | ||
15(S)-HETE Ethanolamide is a specialized lipid that exhibits unique interactions with cellular membranes, influencing lipid bilayer stability and dynamics. Its structure allows for specific binding to proteins involved in signaling pathways, potentially altering their activity. The compound participates in lipid metabolism, acting as a substrate for various enzymatic reactions. Additionally, its presence can modulate the biophysical properties of membranes, affecting fluidity and organization. | ||||||
Linoleamide | 3072-13-7 | sc-221852 sc-221852A | 10 mg 50 mg | $82.00 $347.00 | 2 | |
Linoleamide is a fatty acid amide that exhibits unique properties in lipid metabolism and membrane interactions. Its hydrophobic tail enhances its affinity for lipid bilayers, promoting structural integrity and fluidity. Linoleamide can modulate the activity of various enzymes and receptors through specific molecular interactions, influencing lipid signaling pathways. Additionally, it participates in the formation of lipid microdomains, affecting cellular communication and membrane organization. |