Issue 0, 1981

Heterocyclic prostaglandin analogues. Part 3. The relationship of configuration to biological activity for some hydantoin prostaglandin analogues

Abstract

The enantiomers of the two diastereoisomers of 5-(6-carboxyhexyl)-1-(3-cyclohexyl-3-hydroxypropyl)hydantoin have been synthesised. Potent inhibition of platelet aggregation in this series is associated with the configuration corresponding to that in the natural inhibitors, such as prostaglandins E1 and D2.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 706-711

Heterocyclic prostaglandin analogues. Part 3. The relationship of configuration to biological activity for some hydantoin prostaglandin analogues

M. A. Brockwell, A. G. Caldwell, N. Whittaker and M. J. Begley, J. Chem. Soc., Perkin Trans. 1, 1981, 706 DOI: 10.1039/P19810000706

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