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L-threo-Sphingosine (d18:1)

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    L-<wbr/><em>threo</em>-<wbr/>Sphingosine (d18:1)
  • L-<wbr/><em>threo</em>-<wbr/>Sphingosine (d18:1)
Cat No: 10010541
Biochemicals - Kinase Inhibitors
Cayman

Sphingosines are long-chain base precursors of cellular sphingolipids and are used directly in the synthesis of ceramide. Sphingosine can exist in four stereoisomers, however only D-erythro-sphingosine occurs naturally. L-threo-Sphingosine C-18, an ana...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2S-amino-4E-octadecene-1,3S-diol
Correlated keywords:
  • D-erythro-sphingosine sphingolipids ceramides serines palmitoyltransferases protein kinases C cells proliferations cytoskeletal organization inhibitor inhibition inhibits PKCsSPTs
Product Overview:
Sphingosines are long-chain base precursors of cellular sphingolipids and are used directly in the synthesis of ceramide. Sphingosine can exist in four stereoisomers, however only D-erythro-sphingosine occurs naturally. L-threo-Sphingosine C-18, an analog of D-erythro-sphingosine, inhibits protein kinase C in mixed micelle assays with 50% inhibition at 2.2 mol % making it a slightly more potent inhibitor compared to D-erythro-sphingosine (50% inhibition at 2.8 mol %) or other analogs of shorter alkyl chain length.{15200} Addition of L-threo-Sphingosine C-18 to primary cultured cerebellar cells does not decrease serine palmitoyltransferase (SPT) activity, the rate-limiting enzyme in ceramide biosynthesis, whereas under similar conditions D-erythro-sphingosine inhibits SPT activity.{15203}
Size 5 mg
Shipping dry ice
CAS Number 25695-95-8
Molecular Formula C18H37NO2
SMILES CCCCCCCCCCCCC/C=C/[C@H](O)[C@@H](N)CO
Molecular Weight 299,5
Formulation A crystalline solid
Purity >98%
Custom Code 2933.49
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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