16-Phenoxy tetranor prostaglandin f2alpha

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Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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16-Phenoxy tetranor prostaglandin f2alpha manufacturers
16-Phenoxy tetranor prostaglandin f2alpha Basic information
Product Name:16-Phenoxy tetranor prostaglandin f2alpha
Synonyms:9ALPHA,11ALPHA,15R-TRIHYDROXY-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID;16-phenoxy tetranor Prostaglandin F2α;16-phenoxy-omega-tetranor-PGF2 alpha;5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-phenoxy-1-buten-1-yl]cyclopentyl]-, (5Z)-;16-Phenoxy tetranor prostaglandin f2alpha
CAS:51705-19-2
MF:C22H30O6
MW:390.47
EINECS:
Product Categories:
Mol File:51705-19-2.mol
16-Phenoxy tetranor prostaglandin f2alpha Structure
16-Phenoxy tetranor prostaglandin f2alpha Chemical Properties
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
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MSDS Information
16-Phenoxy tetranor prostaglandin f2alpha Usage And Synthesis
Description16-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.
Uses16-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).
16-Phenoxy tetranor prostaglandin f2alpha Preparation Products And Raw materials
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