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1,2-Distearoyl-sn-glycerol

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    1,2-<wbr/>Distearoyl-<wbr/><em>sn</em>-<wbr/>glycerol
  • 1,2-<wbr/>Distearoyl-<wbr/><em>sn</em>-<wbr/>glycerol
Cat No: 15079
Biochemicals - Lipids
Cayman

1,2-Diacylglycerols (DAGs) are formed in cells through the hydrolysis of phospatidyliositol 4,5-bisphosphate by phospholipase C. They have important roles in signal transduction, as in their activation of some isoforms of PKC.{24394} In addition, DAGs ...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 1,2-distearoyl-sn-glycerol
Correlated keywords:
  • 1429-59-0 111736-26-6 lipids diacylglycerols signals transductions DAGs cells hydrolysis phospatidyliositol 4,5-bisphosphate bisphosphate phospholipase C PKCs isoforms phosphatidic acids 18:0 18 0 180 saturated long-chains long chains stearic sn-1 sn-2 sns 1 2 sn1 sn2 4 5 roles signal transductions activations kinases signaling bioactives distearoyl glycerol forms positions
Product Overview:
1,2-Diacylglycerols (DAGs) are formed in cells through the hydrolysis of phospatidyliositol 4,5-bisphosphate by phospholipase C. They have important roles in signal transduction, as in their activation of some isoforms of PKC.{24394} In addition, DAGs are modified by DAG kinases, reducing signaling through DAG while generating bioactive phosphatidic acids.{7274,24395} 1,2-Distearoyl-sn-glycerol is a form of DAG containing the saturated long-chain (18:0) stearic acid at both the sn-1 and the sn-2 position.
Size 100 mg
Shipping dry ice
CAS Number 10567-21-2
Molecular Formula C39H76O5
SMILES OC[C@H](OC(CCCCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O
Molecular Weight 625
Formulation A crystalline solid
Purity ≥98%
Custom Code 2915.70
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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