Items 31 to 40 of 64 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
C-8 Ceramide | 74713-59-0 | sc-205233 sc-205233A sc-205233B | 1 mg 5 mg 25 mg | $19.00 $63.00 $228.00 | 1 | |
C-8 Ceramide is a distinctive sphingolipid characterized by its long-chain fatty acid structure, which facilitates unique interactions within cellular membranes. This ceramide plays a pivotal role in lipid bilayer organization, influencing membrane fluidity and stability. Its hydrophobic tail promotes specific protein interactions, modulating signaling pathways related to cell growth and apoptosis. Additionally, C-8 Ceramide participates in the formation of lipid rafts, crucial for cellular compartmentalization and communication. | ||||||
D-erythro-Sphingosine C-15 | 86555-28-4 | sc-358749 sc-358749A | 1 mg 5 mg | $100.00 $395.00 | ||
D-erythro-Sphingosine C-15 is a notable sphingolipid distinguished by its unique stereochemistry and extended hydrocarbon chain, which enhances its capacity for membrane integration. This compound exhibits specific binding affinities with membrane proteins, influencing lipid raft dynamics and cellular signaling. Its structural properties facilitate interactions with various biomolecules, potentially impacting cellular processes such as differentiation and stress response. The compound's hydrophobic characteristics also contribute to its role in membrane microdomain formation. | ||||||
C-6 NBD Ceramide | 86701-10-2 | sc-204661 sc-204661A | 1 mg 5 mg | $312.00 $872.00 | 1 | |
C-6 NBD Ceramide is a distinctive sphingolipid characterized by its fluorescent NBD (nitrobenzoxadiazole) moiety, which allows for real-time visualization in biological systems. This ceramide variant plays a crucial role in modulating membrane fluidity and stability, influencing lipid bilayer organization. Its unique structure promotes interactions with specific proteins, affecting signaling pathways and cellular responses. Additionally, the compound's hydrophobic nature aids in the formation of lipid microdomains, enhancing its functional versatility. | ||||||
C8 Dihydroceramide | 145774-33-0 | sc-205611 sc-205611A | 5 mg 25 mg | $67.00 $275.00 | ||
C8 Dihydroceramide is a notable sphingolipid distinguished by its unique hydrophobic tail, which enhances its ability to integrate into lipid bilayers. This integration influences membrane dynamics and facilitates the formation of lipid rafts, crucial for cellular signaling. The compound's structural features promote specific interactions with membrane proteins, modulating their activity and impacting various cellular processes. Its role in cellular architecture underscores its importance in maintaining membrane integrity and function. | ||||||
C-8 Ceramide-1-phosphate | 158983-53-0 | sc-223851 sc-223851A | 1 mg 5 mg | $150.00 $562.00 | ||
C-8 Ceramide-1-phosphate is a distinctive sphingolipid characterized by its phosphate group, which imparts a polar head that enhances its solubility in aqueous environments. This property facilitates its interaction with various signaling molecules and proteins, playing a pivotal role in cellular communication pathways. Additionally, its unique structure allows for the formation of lipid microdomains, influencing membrane fluidity and stability, thereby affecting cellular responses to environmental stimuli. | ||||||
C-12 NBD Ceramide | 202850-01-9 | sc-205232 sc-205232A | 1 mg 5 mg | $302.00 $1342.00 | ||
C-12 NBD Ceramide is a specialized sphingolipid featuring a fluorescent NBD (nitrobenzoxadiazole) moiety, which enables real-time visualization of lipid dynamics within cellular membranes. Its elongated hydrocarbon chain enhances hydrophobic interactions, promoting membrane integration and influencing lipid raft formation. This ceramide variant participates in intricate signaling cascades, modulating cellular responses through specific protein interactions and altering membrane properties, thus impacting cellular homeostasis. | ||||||
FTY720 (R)-Phosphate | 402616-23-3 | sc-221638 sc-221638A | 500 µg 1 mg | $75.00 $190.00 | ||
FTY720 (R)-Phosphate is a bioactive sphingolipid derivative that plays a pivotal role in cellular signaling pathways. Its unique phosphate group facilitates interactions with sphingosine-1-phosphate receptors, influencing cellular migration and proliferation. The compound exhibits distinct lipid bilayer properties, enhancing membrane fluidity and stability. Additionally, it modulates intracellular calcium levels, thereby affecting various downstream signaling cascades and cellular functions. | ||||||
C2 Phytoceramide | 475995-69-8 | sc-223853 sc-223853A | 1 mg 5 mg | $59.00 $245.00 | ||
C2 Phytoceramide is a bioactive sphingolipid that contributes to cellular membrane integrity and signaling. Its unique structure allows for specific interactions with lipid rafts, enhancing membrane organization and fluidity. This compound participates in the regulation of ceramide metabolism, influencing pathways related to cell growth and apoptosis. Additionally, C2 Phytoceramide can impact the formation of lipid domains, affecting protein localization and function within the membrane. | ||||||
NBD-FTY720 analog | sc-222046 sc-222046A | 100 µg 500 µg | $39.00 $239.00 | |||
NBD-FTY720 phenoxy (hydrochloride) is a sphingolipid derivative that exhibits unique interactions with cellular membranes, particularly influencing lipid bilayer dynamics. Its structure facilitates the modulation of sphingolipid metabolism, impacting signaling pathways associated with cellular stress responses. This compound can alter membrane permeability and fluidity, potentially affecting the distribution and activity of membrane proteins. Its distinct molecular characteristics enable it to engage in specific lipid-protein interactions, influencing cellular communication and homeostasis. | ||||||
2-Azido-1,3-di-o-pivaloyl-D-erythro-sphingosine | sc-213763 | 20 mg | $330.00 | |||
2-Azido-1,3-di-o-pivaloyl-D-erythro-sphingosine is a sphingolipid analog characterized by its azido group, which enhances its reactivity in click chemistry applications. This compound can participate in selective conjugation reactions, facilitating the study of lipid interactions and cellular processes. Its unique pivaloyl modifications contribute to its hydrophobicity, influencing membrane incorporation and stability, while also affecting lipid raft formation and cellular signaling pathways. |