17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester

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CAS:195503-20-9
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CAS:195503-20-9
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17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Basic information
Product Name:17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester
Synonyms:17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester;17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Exclusive;SPNWWFJGYHYDNY-HCAGXNQISA-N;17-trifluoromethylphenyl trinor Prostaglandin F2.alpha. methyl ester;17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester;17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Exclusive;5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-5-[3-(trifluoromethyl)phenyl]-1-penten-1-yl]cyclopentyl]-, methyl ester, (5Z)-
CAS:195503-20-9
MF:C25H33F3O5
MW:470.52
EINECS:
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Mol File:195503-20-9.mol
17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Structure
17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Chemical Properties
Boiling point 556.7±50.0 °C(Predicted)
density 1.246±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
pka14.25±0.20(Predicted)
Safety Information
MSDS Information
17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Usage And Synthesis
DescriptionProstaglandin F (PGF), acting through the FP receptor, causes smooth muscle contraction and exhibits potent luteolytic activity.1,2,3 17-trifluoromethylphenyl trinor PGF is an analog of PGF 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 PGF methyl ester is a lipophilic analog of 17-trifluoromethylphenyl trinor PGF. Methyl esters of PGs serve as prodrugs, as they are efficiently hydrolyzed in certain tissues to generate the bioactive free acid.
References1. Samuelsson, B., Goldyne, M., Granstr?m, E., et al. Prostaglandins and thromboxanes Annu. Rev. Biochem. 47,997-1029(1978).
2. Speroff, L., and Ramwell, P.W. Prostaglandins in reproductive physiology Am. J. Obstet. Gynecol. 107(7),1111-1130(1970).
3. Crankshaw, D.J., and Gaspar, V. Pharmacological characterization in vitro of prostanoid receptors in the myometrium of nonpregnant ewes J. Reprod. Fertil. 103(1),55-61(1995).
17-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester Preparation Products And Raw materials
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