Since the discovery that the prostaglandin endoperoxides PGG2 and PGH2 are convertedenzymically to the highly unstable but biologically potent substance thromboxane A2 l-3 by a relatively straightforward mechanism, it has been clear that various synthetic analogs of the PG endoperoxides would be of
The synthesis of prostaglandin endoperoxide analogs
โ Scribed by G.L. Bundy
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 210 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Several years ago, the suggestion was made that the biosynthesis of prostaglandins proceeds through endoperoxide intermediates,',' a hypothesis strongly supported by an elegant oxygen labelling study.? More recently, Samuelsson and his coworkers,'** and Nugteren and Bazelhof' have biosynthesized, isolated and characterized two endoperoxides designated as PGG, and PGR.. These intermediates, despite their fairly short half-life in aqueous buffers (-5 min.), possess an interesting spectrum of biological activity.')*
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