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16-phenoxy tetranor Prostaglandin F2? methyl amide

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    16-<wbr/>phenoxy tetranor Prostaglandin F<sub>2?</sub> methyl amide
  • 16-<wbr/>phenoxy tetranor Prostaglandin F<sub>2?</sub> methyl amide
Cat No: 10010562
Biochemicals - Lipids
Cayman

Prostaglandin F2α (PGF2α) drives luteolysis and smooth muscle contraction by activating the FP receptor. Stable, lipophilic analogs of PGF2α are used to modulate luteolysis and treat glaucoma. 16-phenoxy tetranor PGF2α is a metabolically stable form o...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 9?,11?,15R-trihydroxy-16-phenoxy-17,18,19,20-tetranor-prosta-5Z,13E-dien-1-oic acid, methyl amide
Correlated keywords:
  • prostaglandins F2? PGF2? FP receptors analogs glaucoma luteolysis reproductive biology intraocular pressure IOP PGs
Product Overview:
Prostaglandin F2α (PGF2α) drives luteolysis and smooth muscle contraction by activating the FP receptor. Stable, lipophilic analogs of PGF2α are used to modulate luteolysis and treat glaucoma. 16-phenoxy tetranor PGF2α is a metabolically stable form of PGF2α containing a 16-phenoxy group at the ω-terminus. It binds to the FP receptor on ovine luteal cells with much greater affinity (440%) than PGF2α.{2058} 16-phenoxy tetranor PGF2α methyl amide is a lipophilic analog of 16-phenoxy tetranor PGF2α. Methyl amides of PGs may serve as prodrugs, as they are hydrolyzed in certain tissues to generate the bioactive free acid.
Size 500 µg
Shipping dry ice
Molecular Formula C23H33NO5
SMILES O[C@@H]1[C@H](C/C=C\CCCC(NC)=O)[C@@H](/C=C/[C@@H](O)COC2=CC=CC=C2)[C@H](O)C1
Molecular Weight 403,5
Formulation A solution in ethanol
Purity ≥98%
Custom Code 2937.50
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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