| Identification | Back Directory | [Name]
16-PHENOXY TETRANOR PROSTAGLANDIN F2ALPHA | [CAS]
51705-19-2 | [Synonyms]
16-phenoxy-omega-tetranor-PGF2 alpha
16-phenoxy tetranor Prostaglandin F2α
16-PHENOXY TETRANOR PROSTAGLANDIN F2ALPHA
9ALPHA,11ALPHA,15R-TRIHYDROXY-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID
5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-phenoxy-1-buten-1-yl]cyclopentyl]-, (5Z)- | [Molecular Formula]
C22H30O6 | [MDL Number]
MFCD00135252 | [MOL File]
51705-19-2.mol | [Molecular Weight]
390.47 |
| Chemical Properties | Back Directory | [storage temp. ]
Store at -20°C | [solubility ]
DMF: >100 mg/ml (from Fluprostenol); DMSO: >100 mg/ml (from Fluprostenol); Ethanol: >100 mg/ml (from Fluprostenol); PBS pH 7.2: >0.8 mg/ml (from 17-phenyl tri |
| Hazard Information | Back Directory | [Description]
16-phenoxy PGF2α is a metabolically stable analog of PGF2α. It binds to the FP receptor on ovine luteal cells with much greater affinity (440%) than PGF2α. | [Uses]
16-phenoxy tetranor Prostaglandin F2α (16-phenoxy tetranor PGF2α) is a metabolically stable analog of PGF2α. It binds to the FP receptor on ovine luteal cells with much greater affinity (440%) than PGF2α. | [References]
[1] Balapure, et al. Structural requirements for prostaglandin analog interaction with the ovine corpus luteum prostaglandin F2α receptor. Biochem. Pharmacol. 38(14), 2375-2381 (1989). |
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