€129.00 €109.65
Prostaglandin J2 (PGJ2) is a metabolite of PGD2 (Item No. 12010) and an agonist of the prostaglandin D2 (PGD2) receptor subtypes DP1 and DP2/CRTH.{9080,11291} It is formed from PGD2 by spontaneous dehydration.{58890} PGJ2 binds to DP1 and DP2/CRTH receptors (Kis = 0.9 and 6.6 nM, respectively) and either increases or inhibits the production of cAMP (EC50s = 1.2 and 13.1 nM, respectively, in HEK293 cells expressing the human receptors).{9080,11291} PGJ2 is neurotoxic and induces apoptosis, oxidative stress, and the accumulation of ubiquitinated proteins in the brain.{58891} It promotes the cleavage of amyloid precursor protein (APP) by ?- and ?-secretase in primary rat cerebral cortical neurons when used at a concentration of 10 µM.{58890} The levels of PGJ2 increase in the brain after stroke or traumatic brain injury (TBI) in rodents and it accumulates in the spinal cord of patients with sporadic amyotrophic lateral sclerosis (ALS).
Territorial Availability: Available through Bertin Technologies only in France
| Size | 1 mg, 10 mg, 5 mg, 500 µg |
|---|---|
| Shipping | dry ice |
| CAS number | 60203-57-8 |
| Molecular formula | C20H30O4 |
| Smiles | CCCCC[C@H](O)/C=C/[C@H]([C@@H](C/C=CCCCC(O)=O)C=C1)C1=O, CCCCC[C@H](O)/C=C/[C@H]([C@@H](C/C=CCCCC(O)=O)C=C1)C1=O, CCCCC[C@H](O)/C=C/[C@H]([C@@H](C/C=CCCCC(O)=O)C=C1)C1=O, CCCCC[C@H](O)/C=C/[C@H]([C@@H](C/C=CCCCC(O)=O)C=C1)C1=O |
| Molecular weight | 334,5 |
| Custom code | 2937.50 |
| Formulation | A solution in methyl acetate |
| Purity | ≥95% |
| UNSPSC code | 12352100 |
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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