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Synthesis and pharmacological activities of 13-dehydro derivatives of primary prostaglandins
Authors:T Tanami  K Kameo  N Ono  T Nakagawa  S Annou  M Tsuboi  K Tani  S Okamoto  F Sato
Affiliation:Research Center, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.
Abstract:13-Dehydro derivatives of prostaglandin E1, E2, E3, F1 alpha and F2 alpha were synthesized. Compared with natural prostaglandins, 13-dehydro analogues were found to exhibit more potent inhibitory activity against human platelet aggregation and relaxation of guinea-pig isolated trachea, while they showed less potent activity of contraction of guinea-pig isolated ileum.
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