Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Prostaglandin F2α (PGF2α) activates the FP receptor, promoting smooth muscle contraction and luteolysis. 17-phenyl trinor PGF2α binds the FP receptor on ovine luteal cells with a relative potency of 756% compared to that of PGF2α. It is produced in vivo by the hydrolysis of 17-phenyl trinor PGF2α ethyl amide. 17-phenyl trinor PGF2α ethyl amide is used to reduce intraocular pressure related to glaucoma. 17-phenyl trinor PGF2α cyclopropyl methyl amide is a lipophilic analog of 17-phenyl trinor PGF2α. Amides of PGs may serve as prodrugs, as they are hydrolyzed in certain tissues to generate the bioactive free acid.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | 35 days | $ 183.00 | |
5 mg | 35 days | $ 793.00 | |
10 mg | 35 days | $ 1,430.00 |
Description | Prostaglandin F2α (PGF2α) activates the FP receptor, promoting smooth muscle contraction and luteolysis. 17-phenyl trinor PGF2α binds the FP receptor on ovine luteal cells with a relative potency of 756% compared to that of PGF2α. It is produced in vivo by the hydrolysis of 17-phenyl trinor PGF2α ethyl amide. 17-phenyl trinor PGF2α ethyl amide is used to reduce intraocular pressure related to glaucoma. 17-phenyl trinor PGF2α cyclopropyl methyl amide is a lipophilic analog of 17-phenyl trinor PGF2α. Amides of PGs may serve as prodrugs, as they are hydrolyzed in certain tissues to generate the bioactive free acid. |
Synonyms | 17-phenyl trinor Prostaglandin F2α cyclopropyl methyl amide |
Molecular Weight | 441.612 |
Formula | C27H39NO4 |
CAS No. | 1138395-10-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMF: 25 mg/mL
PBS (pH 7.2): 0.25 mg/mL
Ethanol: 50 mg/mL
DMSO: 25 mg/mL
Acetonitrile: 3 mg/mL
You can also refer to dose conversion for different animals. More
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17-phenyl trinor Prostaglandin F2α cyclopropyl methyl amide 1138395-10-4 17phenyl trinor Prostaglandin F2α cyclopropyl methyl amide 17-phenyl trinor Prostaglandin F-2α cyclopropyl methyl amide 17 phenyl trinor Prostaglandin F2α cyclopropyl methyl amide inhibitor inhibit