Ceramide, with the CAS number 71812-11-8, is a complex glycosphingolipid that plays a crucial role in cellular structure and function. It is characterized by a sphingoid base backbone, which is linked to various sugar moieties, including N-acetyl-neuraminic acid and multiple galactose residues. This structure contributes to its biological significance, particularly in cell signaling, membrane integrity, and the formation of lipid rafts. Ceramides are known to be involved in various physiological processes, including apoptosis, differentiation, and inflammation. The presence of acetylamino and deoxy sugars in its structure enhances its functional diversity and interaction with other biomolecules. Additionally, ceramides are important in skin health, acting as a barrier to prevent moisture loss and protect against environmental damage. Their complex structure and functional roles make them a subject of interest in both biochemistry and pharmacology, particularly in the context of skin diseases and metabolic disorders.

Ceramide,1-O-[O-(N-acetyl-a-neuraminosyl)-(2®3)-O-[O-6-deoxy-a-L-galactopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1®4)]-O-b-D-galactopyranosyl-(1®4)-b-D-glucopyranosyl]-

71812-11-8: Ceramide, with the CAS number 71812-11-8, is a complex glycosphingolipid that plays a crucial role in cellular structure and function. It is characterized by a sphingoid base backbone, which is linked to various sugar moieties, including N-acetyl-neuraminic acid and multiple galactose residues. This structure contributes to its biological significance, particularly in cell signaling, membrane integrity, and the formation of lipid rafts. Ceramides are known to be involved in various physiological processes, including apoptosis, differentiation, and inflammation. The presence of acetylamino and deoxy sugars in its structure enhances its functional diversity and interaction with other biomolecules. Additionally, ceramides are important in skin health, acting as a barrier to prevent moisture loss and protect against environmental damage. Their complex structure and functional roles make them a subject of interest in both biochemistry and pharmacology, particularly in the context of skin diseases and metabolic disorders.

<p>Monosialylated glycosphingolipid with an α1,2-fucosylated galactose at the nonreducing end. The moluecule is minimally expressed in healthy tissues but has high prevalence in some tumours such as small cell lung cancer (SCLC). Fucosyl-GM1 ganglioside is a potential tumour marker for SCLC and a potential antigen target for immunotherapy.</p>

CAS 71812-11-8

Ceramide,1-O-[O-(N-acetyl-a-neuraminosyl)-(2®3)-O-[O-6-deoxy-a-L-galactopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1®4)]-O-b-D-galactopyranosyl-(1®4)-b-D-glucopyranosyl]-

Fucosyl-GM1 ganglioside

Ref: 3D-OF63366