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5(S),6(R)-11-trans DiHETE

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    5(S),6(R)-<wbr/>11-<wbr/><em>trans</em> DiHETE
  • 5(S),6(R)-<wbr/>11-<wbr/><em>trans</em> DiHETE
Cat No: 10009628
Biochemicals - Lipids
Cayman

5(S),6(R)-11-trans DiHETE is a C-11 double bond isomer of 5(S),6(R)-DiHETE that is formed by the enzymatic isomerization of 5(S),6(R)-DiHETE by a membrane bound factor.{14924} 5(S),6(R)-11-trans DiHETE has been found in rat kidney homogenates and is p...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 11-trans-5S,6R-dihydroxy-7E,9E,11E,14Z-eicosatetraenoic acid
Correlated keywords:
  • 5(S),6(S)-diHETE LTA4 LTB4 6-trans-12-epi epoxides hydrolase kidneys rats homogenates
Product Overview:
5(S),6(R)-11-trans DiHETE is a C-11 double bond isomer of 5(S),6(R)-DiHETE that is formed by the enzymatic isomerization of 5(S),6(R)-DiHETE by a membrane bound factor.{14924} 5(S),6(R)-11-trans DiHETE has been found in rat kidney homogenates and is potentially formed by the epoxide hydrolase pathway in this tissue.{14924} The isomerase activity responsible for the conversion of leukotriene B4 (LTB4) to 6-trans LTB4 in rat kidney homogenates has also been implicated in its formation.{14925} 5(S),6(R)-11-trans DiHETE is not a substrate for soybean lipoxygenase.{14924} The biological activity of 5(S),6(R)-11-trans DiHETE has not been reported.
Size 25 µg
Shipping dry ice
CAS Number 129263-59-8
Molecular Formula C20H32O4
SMILES CCCCC/C=C\C/C=C/C=C/C=C/[C@@H](O)[C@@H](O)CCCC(O)=O
Molecular Weight 336,5
Formulation A solution in ethanol
Purity ≥95%
Custom Code 2916.19
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.

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