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HomeProduct name list17-PHENYL TRINOR PGF2ALPHA-IPR

17-PHENYL TRINOR PGF2ALPHA-IPR

17-PHENYL TRINOR PGF2ALPHA-IPR Structural

What is 17-PHENYL TRINOR PGF2ALPHA-IPR?

Description

17-phenyl trinor PGF N-ethyl amide is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive drug, sold under the Allergan trade name Bimatoprost. The N-ethyl amide prostaglandin prodrugs are converted to the active free acid more slowly than the analogous prostaglandin ester prodrugs such as latanoprost. This product is the isopropyl ester of the free acid prostaglandin which corresponds to Bimatoprost. The free acid, 17-phenyl trinor PGF, is a potent FP receptor agonist. In human and animal models of glaucoma, FP receptor agonist activity corresponds very closely with intraocular hypotensive activity. The 17-phenyl trinor PGF isopropyl ester derivative was examined for IOP-lowering activity during the development of latanoprost. At the dose of 3 μg/eye in the monkey, 17-phenyl trinor PGF isopropyl ester was the most potent analog tested in reducing IOP, lowering the IOP 1.3 mm Hg below the level achieved by latanoprost. However, this derivative was also significantly more irritating to the eye than latanoprost.

The Uses of 17-PHENYL TRINOR PGF2ALPHA-IPR

PhDH 100A can be useful in the determination of prostaglandin analogs in cosmetic products by high performance liquid chromatography with tandem mass spectrometry.

What are the applications of Application

17-phenyl trinor PGF2α isopropyl ester is a F-series prostaglandin analog and potent FP receptor agonist

Definition

ChEBI: 17-phenyl-trinor-PGF2alpha isopropyl ester is a prostanoid.

Properties of 17-PHENYL TRINOR PGF2ALPHA-IPR

Boiling point: 573.4±50.0 °C(Predicted)
Density  1.141
storage temp.  Store at -20°C
solubility  DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 50 mg/ml; Ethanol:PBS (pH 7.2) (1:1): 1 mg/ml
pka 14.25±0.20(Predicted)

Safety information for 17-PHENYL TRINOR PGF2ALPHA-IPR

Computed Descriptors for 17-PHENYL TRINOR PGF2ALPHA-IPR

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