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雄甾烯-17-硫缩酮。第二篇通讯:替泼那定及(11β,17α)-17-(乙硫基)-9α-氟-17-[2-(氟乙基)硫基]-11β-羟基-雄甾-1,4-二烯-3-酮的药理学特征,具有强效和选择性局部抗炎活性的结构新颖的20-硫代甾体。

Androstene-17-thioketals. 2nd communication: pharmacological profiles of tipredane and (11 beta, 17 alpha)-17-(ethylthio)-9 alpha-fluoro-17-[2-(fluoroethyl)thio]-11 beta-hydroxy-androsta-1,4-dien-3-one, structurally novel 20-thiasteroids possessing potent and selective topical antiinflammatory activity.

作者信息

Lutsky B N, Millonig R C, Wojnar R J, Free C A, Devlin R G, Varma R K, Karanewsky D S

出版信息

Arzneimittelforschung. 1986 Dec;36(12):1787-95.

PMID:3494459
Abstract

Two structurally novel alkylthio-substituted steroids, (11 beta, 17 alpha)-17-(ethylthio)-9 alpha-fluoro-11 beta-hydroxy-17-(methylthio)andro-1,4-dien-3-one (tipredane, SQ 27,239) and (11 beta, 17 alpha)-(ethylthio)-9 alpha-fluoro-17-[2-(fluoroethyl) thio]-11 beta-hydroxy-androsta-1,4-dien-3-one (SQ 28,300) were compared to presently available topical corticosteroids for in vitro and in vivo glucocorticoid and antiinflammatory activities. Based upon results of in vitro assays, in vivo antiinflammatory tests in mice, and human vasoconstriction measurements, the thiasteroids most closely resemble moderately potent to highly potent corticoids. These compounds display more modest activity in topical antiinflammatory assays using rats. Both tipredane and SQ 28,300 exhibit favorable separation of local antiinflammatory activity from systemic effects on thymus and hypothalamic-pituitary-adrenal axis function, most probably due to rapid metabolic inactivation. As such, these compounds represent potentially safer therapy for topical treatment of corticoid-responsive skin diseases and bronchopulmonary conditions in humans.

摘要

将两种结构新颖的烷硫基取代甾体,即(11β,17α)-17-(乙硫基)-9α-氟-11β-羟基-17-(甲硫基)雄甾-1,4-二烯-3-酮(替泼尼旦,SQ 27239)和(11β,17α)-(乙硫基)-9α-氟-17-[2-(氟乙基)硫基]-11β-羟基雄甾-1,4-二烯-3-酮(SQ 28300),与目前可用的局部用皮质类固醇进行体外和体内糖皮质激素及抗炎活性比较。根据体外试验结果、小鼠体内抗炎试验以及人体血管收缩测量结果,硫代甾体与中效至高效皮质类固醇最为相似。这些化合物在使用大鼠的局部抗炎试验中表现出较为适度的活性。替泼尼旦和SQ 28300在局部抗炎活性与对胸腺及下丘脑-垂体-肾上腺轴功能的全身效应之间均表现出良好的分离,这很可能是由于快速的代谢失活所致。因此,这些化合物代表了对人类皮质类固醇反应性皮肤病和支气管肺部疾病进行局部治疗的潜在更安全疗法。

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