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U-46619 Glycine methyl ester

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    U-46619 Glycine methyl ester
  • U-46619 Glycine methyl ester
Cat No: 10010522
Biochemicals - Lipids
Cayman

U-46619 is a stable analog of the endoperoxide PGH2, and a TP receptor agonist.{8322} It exhibits properties similar to TXA2, causing platelet shape change, aggregation, and contraction of vascular smooth muscle.{490,714} Mean EC50 values for shape ch...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 9,11-dideoxy-9?,11?-methanoepoxy-prosta-5Z,13E-dien-1-oic acid, methyl ester
Correlated keywords:
  • U46619 PGH-2 TXA-2 C1
Product Overview:
U-46619 is a stable analog of the endoperoxide PGH2, and a TP receptor agonist.{8322} It exhibits properties similar to TXA2, causing platelet shape change, aggregation, and contraction of vascular smooth muscle.{490,714} Mean EC50 values for shape change in human, rat, and rabbit platelets are 4.8, 6.0, and 7.3 nM respectively, and for aggregation, are 82, 145, and 65 nM, respectively.{1168} U-46619 glycine methyl ester contains a modification at the C-1 position of U-46619 that may uniquely alter its binding properties to the TP receptor or any of the PGH2-metabolizing enzymes. As a stable PGH2 analog, it could therefore be a useful tool to explore the inhibition of various enzymes in the arachidonic acid metabolic pathway. U-46619 glycine methyl ester may also serve as a lipophilic prodrug form of U-46619 that will alter its distribution and pharmacokinetic properties. There are no published reports on the biological activity of U-46619 glycine methyl ester.
Size 25 µg
Shipping dry ice
Molecular Formula C24H39NO5
SMILES CCCCCC(O)/C=C/[C@H]1C2OCC(C2)C1C/C=C\CCCC(=O)NCC(=O)OC
Molecular Weight 421,6
Formulation A solution in methyl acetate
Purity >98%
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.

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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