The synthesis of 2,3-dinor-6-oxo-prostaglandin F,c, the major metabolite of prostacyclin, from the prostaglandin lactone intermediate ( 2) is reported.
Use of a novel colour reaction in the chromatography of 6-oxo-prostaglandin F1a and related prostaglandins
β Scribed by F.B. Ubatuba
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 950 KB
- Volume
- 161
- Category
- Article
- ISSN
- 1873-3778
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β¦ Synopsis
6-Oxo-prostaglandin FLa (6-0x0-PGF,,), derivatized by methylation, methoxylation and silylation, emerged from OV-1 and OV-17 silicone gas-liquid chromatographic columns as one major peak (equivalent chain length = 25.1). A standardization curve, constructed using pure 6-oxo-PGF,, enabled quantificatiorn down to 5 ng. Silicic acid column chromatography effectively separated 6-oxo-PGF,, (free acid) from all other major prostaglandins. On thin-layer chromatographic silica gel plates, 6-oxo-PGF,, was resolved as discrete spots, well separated from other prostaglandins when developed in 5 out of 7 solvent mixtures. The difference in rate of resolution between 6-oxo-PGF,, and the PGFs in the various solvents afforded another criterion for identification. 6-0x0-PGF,, produced a distinctive yellow chromogen on thin-layer chromatographic silica gel plates sprayed with an anisaldehyde-sulphuric acid reagent; the colour reaction is specific to 6-oxo-PGF1, and some structurally related prostaglandins.
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