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16-phenoxy tetranor Prostaglandin F2α methyl ester manufacturers
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| | 16-phenoxy tetranor Prostaglandin F2α methyl ester Basic information |
| Product Name: | 16-phenoxy tetranor Prostaglandin F2α methyl ester | | Synonyms: | 16-phenoxy tetranor Prostaglandin F2.alpha. methyl ester;16-phenoxy tetranor Prostaglandin F2α methyl ester Exclusive;16-phenoxy tetranor Prostaglandin F2α methyl ester;5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-phenoxy-1-buten-1-yl]cyclopentyl]-, methyl ester, (5Z)- | | CAS: | 51638-90-5 | | MF: | C23H32O6 | | MW: | 404.5 | | EINECS: | | | Product Categories: | | | Mol File: | 51638-90-5.mol |  |
| | 16-phenoxy tetranor Prostaglandin F2α methyl ester Chemical Properties |
| storage temp. | Store at -20°C | | solubility | DMF: 100 mg/ml; DMSO: 100 mg/ml; Ethanol: 100 mg/ml; PBS (pH 7.2): .5 mg/ml |
| | 16-phenoxy tetranor Prostaglandin F2α methyl ester Usage And Synthesis |
| Description | 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 Prostaglandin F2α (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. 16-phenoxy tetranor PGF2α methyl ester is a lipophilic analog of 16-phenoxy tetranor PGF2α. Methyl esters of PGs serve as prodrugs, as they are efficiently hydrolyzed in certain tissues to generate the bioactive free acid. | | Uses | 16-Phenoxy tetranor Prostaglandin F2α methyl ester is a metabolically stable form of Prostaglandin F2α that can binds to FP receptor. 16-Phenoxy tetranor Prostaglandin F2α methyl ester serves as prodrug that can be hydrolyzed to generate bioactive free acid[1]. | | References | [1] M Hayashi, Prostaglandin analogues possessing antinidatory effects. 2. Modification of the alpha chain. J Med Chem. 1980 May;23(5):525-35. DOI:10.1021/jm00179a011 |
| | 16-phenoxy tetranor Prostaglandin F2α methyl ester Preparation Products And Raw materials |
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