474943-06-1

Basic information

• Product Name: C12 NBD-SPHINGOSINE, BETA-D-LACTOSYL
• Synonyms: C12 NBD-SPHINGOSINE, BETA-D-LACTOSYL;C12 NBD-SPHINGOSINE, B-D-LACTOSYL;N-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)aMino]dodecanoyl]-D-lactosyl-1-1'-sphingosine;C12 NBD Lactosylceramide (d18:1/12:0)
• CAS NO: 474943-06-1
• Molecular Formula: C48H80N4O16
• Molecular Weight: 969.17
• Mol File: 474943-06-1.mol

Chemical Properties

• Appearance: /
• Density: 1.30±0.1 g/cm3(Predicted)
• PKA: 12.79±0.70(Predicted)
• CAS DataBase Reference: C12 NBD-SPHINGOSINE, BETA-D-LACTOSYL(CAS DataBase Reference)
• NIST Chemistry Reference: C12 NBD-SPHINGOSINE, BETA-D-LACTOSYL(474943-06-1)
• EPA Substance Registry System: C12 NBD-SPHINGOSINE, BETA-D-LACTOSYL(474943-06-1)

Safety Data

• Hazardous Substances Data: 474943-06-1(Hazardous Substances Data)

Usage

Uses

Used in Research Applications:
C12 Nbd-sphingosine, beta-D-lactosyl is used as a research tool for studying the metabolism and function of sphingolipids in cells. The fluorescent tag allows researchers to easily visualize and track the compound within cells, providing insights into the role of sphingolipids in cellular processes.
Used in Pharmaceutical Development:
C12 Nbd-sphingosine, beta-D-lactosyl is used as a potential candidate in drug development, given its ability to interact with cell membranes and its potential to influence cellular processes. C12 Nbd-sphingosine, beta-D-lactosyl's properties may contribute to the discovery of new therapeutic agents targeting sphingolipid-related pathways.
Used in Diagnostic Tool Development:
C12 Nbd-sphingosine, beta-D-lactosyl is used as a component in the development of diagnostic tools, particularly for visualizing and tracking cellular processes involving sphingolipids. The fluorescent tag makes it easier to monitor these processes, which could be valuable in detecting and diagnosing diseases related to sphingolipid metabolism.
Used in the Study of Carbohydrate-Binding Proteins and Cell Adhesion:
C12 Nbd-sphingosine, beta-D-lactosyl is used as a research compound in the study of carbohydrate-binding proteins and cell adhesion mechanisms. The addition of lactose enables the compound to interact with these proteins, providing a means to investigate their roles in cellular processes and potentially uncovering new therapeutic targets.