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(±)5(6)-EET-d11

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    (±)5(6)-<wbr/>EET-<wbr/>d<sub>11</sub>
  • (±)5(6)-<wbr/>EET-<wbr/>d<sub>11</sub>
Cat No: 10009984
Biochemicals - Isotopically Labeled Standards
Cayman

(±)5(6)-EET-d11 is intended for use as an internal standard for the quantification of 5(6)-EET by GC- or LC-MS. 5(S),6(R)-EET and 5(R),6(S)-EET are formed via epoxidation of arachidonic acid (Item Nos. 90010
90010.1
10006607) by a variety of cytoc...

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This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (±)5(6)-epoxy-8Z,11Z,14Z-eicosatrienoic-16,16,17,17,18,18,19,19,20,20,20-d11 acid
Correlated keywords:
  • epoxides epoxygenases cytochrome P450 (+/-)5(6)-EpETrEs (+/-)5,6-EpETrEs 5,6-EETs fatty acids deuterated deuterium
Product Overview:
(±)5(6)-EET-d11 is intended for use as an internal standard for the quantification of 5(6)-EET by GC- or LC-MS. 5(S),6(R)-EET and 5(R),6(S)-EET are formed via epoxidation of arachidonic acid (Item Nos. 90010
90010.1
10006607) by a variety of cytochrome P450 (CYP) isoforms, including CYP2B1, CYP2B2, CYP2C11, CYP2C23, and CYP2C24.{60308,39722}
Size 10 µg
Shipping dry ice
Molecular Formula C20H21D11O3
SMILES [2H]C(C([2H])([2H])C([2H])([2H])[2H])([2H])C([2H])([2H])C([2H])([2H])/C=C\C/C=C\C/C=C\C[C@@H](O1)[C@@H]1CCCC(O)=O
Molecular Weight 331,5
Formulation A solution in methyl acetate
Purity ≥99% deuterated forms (d1-d11)
Custom Code 3822.19
UNSPSC code 12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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