Items 41 to 50 of 97 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
AUDA | 479413-70-2 | sc-221276 sc-221276A | 5 mg 10 mg | $48.00 $82.00 | 1 | |
AUDA is a long-chain fatty acid characterized by its unique double bond configuration, which significantly influences its reactivity and interaction with biological membranes. Its distinct molecular structure promotes enhanced solubility in organic solvents, facilitating its role in lipid metabolism. AUDA engages in specific enzymatic pathways, leading to the production of bioactive lipids that modulate cellular functions. Its kinetic properties allow for rapid incorporation into lipid bilayers, affecting membrane dynamics and signaling processes. | ||||||
cis-4,10,13,16-Docosatetraenoic Acid methyl ester | sc-223891 sc-223891A sc-223891B | 1 mg 2.5 mg 5 mg | $27.00 $65.00 $131.00 | |||
Cis-4,10,13,16-Docosatetraenoic Acid methyl ester is a polyunsaturated fatty acid with a unique arrangement of double bonds that enhances its fluidity and flexibility in lipid environments. This structural feature allows for effective integration into cellular membranes, influencing membrane permeability and protein interactions. Its reactivity facilitates participation in lipid peroxidation processes, contributing to the generation of signaling molecules that impact various cellular pathways. | ||||||
D-erythro-N,N,N-Trimethylsphingosine Chloride | sc-218020 | 10 mg | $330.00 | |||
D-erythro-N,N,N-Trimethylsphingosine Chloride is a quaternary ammonium compound that exhibits unique interactions with lipid bilayers, enhancing membrane stability and fluidity. Its trimethylated structure facilitates strong electrostatic interactions with negatively charged phospholipids, influencing membrane dynamics. This compound can modulate ion channel activity and impact cellular signaling pathways, contributing to the regulation of various physiological processes. Its distinctive properties make it a key player in lipid-related research. | ||||||
Myristoleic acid | 544-64-9 | sc-215408 | 100 mg | $158.00 | ||
Myristoleic acid is a monounsaturated fatty acid characterized by its long hydrocarbon chain and a single cis double bond, which imparts distinct fluidity to lipid bilayers. This structural configuration promotes unique interactions with membrane proteins, potentially altering their conformation and activity. Additionally, its presence can influence lipid metabolism pathways, affecting energy storage and utilization, while also participating in the formation of bioactive lipids that modulate cellular signaling. | ||||||
Nonacosanoic Acid | 4250-38-8 | sc-295941 sc-295941A | 1 g 5 g | $460.00 $1615.00 | ||
Nonacosanoic acid, a long-chain saturated fatty acid, exhibits unique properties due to its extensive hydrocarbon chain, which enhances its hydrophobic interactions. This characteristic allows it to form stable aggregates in lipid environments, influencing membrane dynamics and fluidity. Its high molecular weight contributes to distinct phase behavior in lipid mixtures, potentially affecting the organization of lipid rafts and impacting cellular signaling pathways. Additionally, it plays a role in the synthesis of wax esters, contributing to the structural integrity of biological membranes. | ||||||
9(R)-HODE | 10075-11-3 | sc-205192 sc-205192A | 25 µg 50 µg | $75.00 $143.00 | ||
9(R)-HODE, a hydroxy fatty acid, is notable for its role in lipid metabolism and signaling. Its hydroxyl group facilitates unique hydrogen bonding interactions, enhancing its solubility in polar environments. This compound participates in various enzymatic pathways, influencing the synthesis of bioactive lipids. Its presence can modulate membrane fluidity and permeability, impacting cellular responses and interactions with proteins, thereby playing a crucial role in cellular homeostasis. | ||||||
Pinolenic Acid | 16833-54-8 | sc-205437 sc-205437B sc-205437C sc-205437D | 0.5 mg 5 mg 10 mg 25 mg | $39.00 $102.00 $132.00 $233.00 | 1 | |
Pinolenic acid is a polyunsaturated fatty acid characterized by its unique double bond configuration, which influences its reactivity and interaction with biological membranes. This compound exhibits distinct conformational flexibility, allowing it to integrate into lipid bilayers and affect membrane dynamics. Its ability to engage in specific molecular interactions can modulate the activity of enzymes and receptors, thereby influencing metabolic pathways and cellular signaling processes. | ||||||
Stearidonic Acid | 20290-75-9 | sc-360690 sc-360690A sc-360690B sc-360690C sc-360690D | 1 mg 5 mg 10 mg 50 mg 100 mg | $113.00 $538.00 $1019.00 $4896.00 $8507.00 | ||
Stearidonic acid is a polyunsaturated fatty acid notable for its unique structure, featuring multiple double bonds that enhance its reactivity. This compound plays a crucial role in lipid metabolism, participating in the synthesis of longer-chain fatty acids through elongation pathways. Its distinct hydrophobic properties facilitate interactions with proteins and lipids, influencing membrane fluidity and cellular function. Additionally, stearidonic acid can serve as a precursor for bioactive lipids, impacting various physiological processes. | ||||||
9(S)-HpODE | 29774-12-7 | sc-205196 sc-205196A | 100 µg 500 µg | $214.00 $903.00 | ||
9(S)-HpODE is a hydroperoxy fatty acid characterized by its specific stereochemistry and the presence of a hydroperoxide functional group. This compound is involved in lipid peroxidation processes, leading to the formation of reactive oxygen species that can modulate cellular signaling pathways. Its unique structure allows for specific interactions with lipid membranes, potentially altering membrane dynamics and influencing protein activity. Additionally, 9(S)-HpODE can participate in various enzymatic reactions, contributing to the complex network of lipid-derived signaling molecules. | ||||||
cis-10-Nonadecenoic acid | 73033-09-7 | sc-280642 | 250 mg | $114.00 | ||
Cis-10-Nonadecenoic acid is a long-chain unsaturated fatty acid notable for its unique cis configuration, which influences its fluidity and interaction with biological membranes. This structural characteristic enhances its ability to integrate into lipid bilayers, affecting membrane permeability and protein interactions. The acid can undergo various enzymatic transformations, participating in metabolic pathways that regulate energy storage and utilization. Its distinct reactivity also allows it to form esters and amides, contributing to diverse biochemical processes. | ||||||