QLKKMIWGFNMQJQ-JZFYYOKZSA-N manufacturers
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| | QLKKMIWGFNMQJQ-JZFYYOKZSA-N Basic information |
| Product Name: | QLKKMIWGFNMQJQ-JZFYYOKZSA-N | | Synonyms: | QLKKMIWGFNMQJQ-JZFYYOKZSA-N;17-trifluoromethylphenyl trinor Prostaglandin F2.alpha. ethyl amide;9α,11α,15S-trihydroxy-17-trifluoromethylphenyl-18,19,20-trinor-prosta-5Z,13E-dien-1-oic acid, ethyl amide;5-Heptenamide, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-5-[3-(trifluoromethyl)phenyl]-1-penten-1-yl]cyclopentyl]-N-ethyl-, (5Z)-;17-trifluoromethylphenyl trinor Prostaglandin F2α ethyl amide | | CAS: | 1621369-73-0 | | MF: | C26H36F3NO4 | | MW: | 483.56 | | EINECS: | | | Product Categories: | | | Mol File: | 1621369-73-0.mol |  |
| | QLKKMIWGFNMQJQ-JZFYYOKZSA-N Chemical Properties |
| Boiling point | 626.1±55.0 °C(Predicted) | | density | 1.220±0.06 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMF: 25 mg/ml; DMSO: 50 mg/ml; Ethanol: 50 mg/ml; PBS (pH 7.2): .15 mg/ml | | pka | 14.25±0.20(Predicted) |
| | QLKKMIWGFNMQJQ-JZFYYOKZSA-N Usage And Synthesis |
| Description | Prostaglandin F2α (PGF2α), acting through the FP receptor, causes smooth muscle contraction and exhibits potent luteolytic activity. 17-trifluoromethylphenyl trinor Prostaglandin F2α (17-trifluoromethylphenyl trinor PGF2α) is an analog of PGF2α that shares the meta-trifluoromethyl group of travoprost with the 17-phenyl trinor modification of latanoprost. It is anticipated to be a potent and selective agonist of the FP receptor, with potential applications in glaucoma and luteolysis. 17-trifluoromethylphenyl trinor PGF2α ethyl amide is a lipophilic analog of 17-trifluoromethylphenyl trinor PGF2α. Ethyl amides of PGs can serve as prodrugs, as they are hydrolyzed in certain tissues to generate the bioactive free acid. | | Uses | 17-Trifluoromethylphenyl trinor prostaglandin F2α ethyl amide (compound 17-CF3PTPG2α EA) is a lipophilic analog of 17-trifluoromethylphenyl trinor PGF2α[1]. | | References | [1] Wittenberg JB, et al. Determination of prostaglandin analogs in cosmetic products by high performance liquid chromatography with tandem mass spectrometry. J Chromatogr A. 2014;1359:140-146. DOI:10.1016/j.chroma.2014.07.032 |
| | QLKKMIWGFNMQJQ-JZFYYOKZSA-N Preparation Products And Raw materials |
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