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Synthesis of a new series of potent inhibitors of thromboxane A2 biosynthesis

โœ Scribed by E.J. Corey; Stephen G. Pyne; Andrew I. Schafer


Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
206 KB
Volume
24
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


The pyridino prostanoids 2, 12 and lfl have been synthesized (in racemic form) and have been found to be effective inhibitors of the biosynthesis of thromboxane A2 in human platelets QC,, l-3 PM).


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## Abstract For Abstract see ChemInform Abstract in Full Text.

Synthesis of a new prostaglandin endoper
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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