Date published: 2025-9-14

1-800-457-3801

SCBT Portrait Logo
Seach Input

Sphingolipids

Santa Cruz Biotechnology now offers a broad range of sphingolipids for use in various applications. Sphingolipids are a class of complex lipids containing a sphingoid base backbone, which are essential components of cell membranes and play crucial roles in cellular signaling and structural integrity. These compounds are significant in scientific research due to their involvement in numerous biological processes and their impact on cell function and health. In biochemistry and cell biology, sphingolipids are studied to understand their role in membrane structure, signaling pathways, and their influence on cell behavior, including apoptosis, proliferation, and differentiation. Researchers utilize sphingolipids to investigate mechanisms of diseases associated with lipid metabolism disorders and to explore potential targets for novel strategies, although not in a clinical context. In neuroscience, sphingolipids are crucial for studying the function and organization of the nervous system, given their role in myelin sheath formation and neuron function. Environmental scientists study sphingolipids to understand their role in cellular responses to environmental stressors and their potential as biomarkers for environmental monitoring. Additionally, sphingolipids are employed in the development of advanced materials and nanotechnology, where their unique structural properties can be harnessed for creating biomimetic materials and drug delivery systems. Analytical chemists use sphingolipids in techniques such as mass spectrometry and chromatography to analyze lipid compositions and understand lipidomics, the large-scale study of pathways and networks of cellular lipids in biological systems. The broad applications of sphingolipids in scientific research underscore their importance in advancing our knowledge of fundamental biological processes and driving innovations across multiple disciplines. View detailed information on our available sphingolipids by clicking on the product name.

Items 31 to 40 of 64 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

C-8 Ceramide

74713-59-0sc-205233
sc-205233A
sc-205233B
1 mg
5 mg
25 mg
$19.00
$63.00
$228.00
1
(0)

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

86555-28-4sc-358749
sc-358749A
1 mg
5 mg
$100.00
$395.00
(0)

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

86701-10-2sc-204661
sc-204661A
1 mg
5 mg
$312.00
$872.00
1
(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

145774-33-0sc-205611
sc-205611A
5 mg
25 mg
$67.00
$275.00
(0)

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

158983-53-0sc-223851
sc-223851A
1 mg
5 mg
$150.00
$562.00
(0)

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

202850-01-9sc-205232
sc-205232A
1 mg
5 mg
$302.00
$1342.00
(0)

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

402616-23-3sc-221638
sc-221638A
500 µg
1 mg
$75.00
$190.00
(0)

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

475995-69-8sc-223853
sc-223853A
1 mg
5 mg
$59.00
$245.00
(0)

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
(0)

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
(0)

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.