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8-iso-15-keto Prostaglandin F2?

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    8-<wbr/><em>iso</em>-<wbr/>15-<wbr/>keto Prostaglandin F<sub>2?</sub>
  • 8-<wbr/><em>iso</em>-<wbr/>15-<wbr/>keto Prostaglandin F<sub>2?</sub>
Cat No: 10008539
Biochemicals - Lipids
Cayman

8-iso Prostaglandin F2β (8-iso PGF2β) is an isomer of PGF2α of non-enzymatic origin. It is one of 64 possible isomers of PGF2α which can be produced by free radical peroxidation of arachidonic acid. 8-iso PGF2β exhibits very weak contraction of human u...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 9?,11?-dihydroxy-15-oxo-(8?)-prosta-5Z,13E-dien-1-oic acid
Correlated keywords:
  • prostaglandins PGF2a PGF2.alpha. 15-hydroxy PGDH isomers free radicals peroxidation arachidonic acids contractions umbilical veins artery human canine porcine pulmonary isoprostanes metabolites
Product Overview:
8-iso Prostaglandin F2β (8-iso PGF2β) is an isomer of PGF2α of non-enzymatic origin. It is one of 64 possible isomers of PGF2α which can be produced by free radical peroxidation of arachidonic acid. 8-iso PGF2β exhibits very weak contraction of human umbilical vein artery and does not promote aggregation of human whole blood.{11143,11145} However, 8-iso PGF2β moderately contracts both the canine and porcine pulmonary vein, although the effect is much weaker than that exhibited by other isoprostanes such as 8-iso PGE1, 8-iso PGE2, or 8-iso PGF2α.{11144,11146} 8-iso-15-keto PGF2β is a potential metabolite of 8-iso PGF2β via the 15-hydroxy PG dehydrogenase pathway. There are no published reports on the formation or biological activity of 8-iso-15-keto PGF2β.
Size 100 µg
Shipping dry ice
CAS Number 1621482-36-7
Molecular Formula C20H32O5
SMILES O[C@@H]1C[C@@H](O)[C@@H](C/C=C\CCCC(O)=O)[C@H]1/C=C/C(CCCCC)=O
Molecular Weight 352,5
Formulation A solution in methyl acetate
Purity ≥95%
Custom Code 2937.50
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.

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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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