Items 51 to 60 of 401 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
cis-10-Heptadecenoic acid | 29743-97-3 | sc-214727 sc-214727A | 100 mg 500 mg | $82.00 $112.00 | 1 | |
Cis-10-Heptadecenoic acid is a monounsaturated fatty acid notable for its unique cis configuration, which influences its fluidity and packing in lipid bilayers. This structural characteristic enhances membrane permeability and flexibility, facilitating molecular interactions that are crucial for cellular processes. Its unsaturation allows for specific enzymatic pathways, impacting lipid metabolism and energy storage. Additionally, it can participate in transesterification reactions, contributing to the formation of biodiesel and other esters. | ||||||
Cholesteryl nervonate | 60758-73-8 | sc-214703 | 100 mg | $153.00 | ||
Cholesteryl nervonate is a complex lipid characterized by its unique structure, which includes a long-chain fatty acid linked to a sterol backbone. This configuration promotes specific hydrophobic interactions within lipid membranes, enhancing stability and influencing membrane dynamics. Its presence can modulate membrane protein activity and lipid raft formation, impacting cellular signaling pathways. Additionally, it plays a role in the synthesis of sphingolipids, contributing to cellular communication and structural integrity. | ||||||
2-Butenoyl coenzyme A lithium salt | 102680-35-3 | sc-213776 | 5 mg | $337.00 | ||
2-Butenoyl coenzyme A lithium salt is a pivotal intermediate in lipid metabolism, featuring a reactive enoyl group that facilitates acyl transfer reactions. Its unique structure allows for specific interactions with enzymes involved in fatty acid synthesis and degradation, influencing metabolic flux. The compound participates in distinct biochemical pathways, enhancing the efficiency of energy production and storage. Its kinetic properties enable rapid participation in metabolic cycles, underscoring its role in cellular lipid homeostasis. | ||||||
Pam3Cys-Ser-(Lys)4 trihydrochloride | 112208-04-5 | sc-202271 | 2 mg | $423.00 | ||
Pam3Cys-Ser-(Lys)4 trihydrochloride is a synthetic lipopeptide that exhibits unique amphiphilic properties, promoting membrane interactions and enhancing cellular uptake. Its structure, characterized by a lipid tail and a peptide backbone, facilitates specific binding to toll-like receptors, triggering distinct signaling pathways. The compound's ability to form micelles and influence membrane dynamics underscores its role in modulating cellular responses and interactions with lipid bilayers, contributing to its functional versatility. | ||||||
N-heptanoyl-L-Homoserine lactone | 177158-20-2 | sc-205404 sc-205404A | 5 mg 10 mg | $35.00 $88.00 | 1 | |
N-heptanoyl-L-Homoserine lactone is a signaling molecule that plays a crucial role in quorum sensing among bacteria. Its lipid-like structure allows for efficient diffusion across membranes, facilitating intercellular communication. The compound engages in specific interactions with receptor proteins, influencing gene expression and biofilm formation. Its unique acyl chain length contributes to distinct reaction kinetics, impacting the timing and intensity of bacterial responses in various environmental conditions. | ||||||
Stearoyl coenzyme A lithium salt | 193402-48-1 | sc-215906 sc-215906A | 5 mg 10 mg | $198.00 $350.00 | ||
Stearoyl coenzyme A lithium salt is a key lipid involved in fatty acid metabolism, characterized by its ability to form stable complexes with enzymes. This compound participates in acylation reactions, where it donates its acyl group to various substrates, influencing lipid biosynthesis pathways. Its unique structure enhances hydrophobic interactions, promoting membrane fluidity and integrity. Additionally, it plays a role in energy storage and cellular signaling, impacting metabolic regulation. | ||||||
Gitoxigenin | 545-26-6 | sc-215071 sc-215071A | 10 mg 25 mg | $342.00 $705.00 | 1 | |
Gitoxigenin is a steroidal compound notable for its unique hydrophobic interactions, which facilitate its incorporation into lipid bilayers. This integration alters membrane properties, enhancing permeability and fluidity. Gitoxigenin's distinct molecular structure allows it to engage in specific binding with lipid-associated proteins, potentially influencing lipid transport and metabolism. Its behavior in lipid environments can modulate the dynamics of membrane microdomains, affecting cellular communication and signaling. | ||||||
Methyl decanoate | 110-42-9 | sc-215344 sc-215344A | 2.5 g 100 g | $56.00 $82.00 | ||
Methyl decanoate is a fatty acid ester that exhibits unique properties as a lipid. Its hydrophobic nature facilitates interactions with lipid bilayers, enhancing membrane permeability. The compound participates in transesterification reactions, where it can be converted into various fatty acids and alcohols, influencing lipid profiles. Its distinct chain length contributes to its role in modulating phase behavior in membranes, affecting fluidity and stability, which is crucial for cellular function. | ||||||
Methyl linoleate | 112-63-0 | sc-215355 sc-215355A | 1 g 5 g | $56.00 $112.00 | ||
Methyl linoleate is a polyunsaturated fatty acid ester characterized by its dual cis double bonds, which introduce kinks in its hydrocarbon chain, enhancing fluidity in lipid environments. This structural feature allows for unique molecular interactions with proteins and other lipids, influencing membrane dynamics. It participates in lipid metabolism pathways, including β-oxidation, and can serve as a substrate for enzymatic reactions, impacting energy production and signaling processes within cells. | ||||||
beta-Sitosterol acetate | 915-05-9 | sc-291985 sc-291985A | 1 g 5 g | $148.00 $413.00 | 1 | |
Beta-Sitosterol acetate is a phytosterol derivative that exhibits unique hydrophobic interactions due to its rigid steroid structure, which influences membrane integrity and fluidity. Its acetate group enhances solubility in organic solvents, facilitating its role in lipid bilayer formation. This compound can participate in esterification reactions, impacting lipid metabolism and storage. Additionally, its presence in membranes can modulate protein activity and cellular signaling pathways, contributing to overall cellular homeostasis. |