Murinova M Iu, Bagaeva S G, Adler M E, Davydova V A, Lazareva D N
Farmakol Toksikol. 1989 Jan-Feb;52(1):50-3.
The pharmacological properties of 4 derivatives of 11-desoxy-prostaglandins E (uterotonic, luteolytic, hypotensive, anti-inflammatory, diarrhogenic ones and also acute toxicity) were studied. Compound I possessed the uterotonic activity which decreased with an alpha-chain elongation and a radical introduction into a benzene ring. Compounds I and II exhibited the luteotropic properties at low doses and the luteolytic ones at high doses. The compounds under study had the hypotensive activity due to the presence of a benzene ring in a W-chain.
研究了11-去氧前列腺素E的4种衍生物的药理特性(子宫收缩、黄体溶解、降压、抗炎、致腹泻特性以及急性毒性)。化合物I具有子宫收缩活性,该活性随着α链的延长和苯环上引入基团而降低。化合物I和II在低剂量时表现出促黄体生成特性,在高剂量时表现出黄体溶解特性。由于W链中存在苯环,所研究的化合物具有降压活性。