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甾体对睾丸酮假单胞菌3β-羟基甾体氧化还原酶的抑制作用

Inhibition of the 3 beta-hydroxysteroid oxidoreductase of Pseudomonas testosteroni by steroids.

作者信息

Kaufmann G, Schlegel J, Schubert K

出版信息

Endokrinologie. 1979 Apr;73(2):130-3.

PMID:467367
Abstract

55 Steroids of the estratriene and androstane type with substituents in pos. 16 alpha, 17 alpha or 17 beta were tested for inhibition of the 3beta-hydroxysteroid oxidoreductase of Pseudomonas testosteroni. Estratrien-3-ols were strong and competitive inhibitors (Ki less than 1 micron). Substituents in pos. 16 alpha of estradiol influenced the inhibitory activity distinctly. Substituents in 17 alpha- or 17 beta-position were of slight influence. 3-Methoxy estratrienes gave no inhibition of the enzymic 3 beta-OH-dehydrogenation. The 4-unsaturated 3-oxo-steroids tested were moderate inhibitors (Ki 2.4-70 micron). The activity was slightly influenced by 17 alpha-substituents. It was increased by 10 beta-substituents in the order H less than CH3 less than N3. The inhibition test can be used to select and eliminate very strong synthetic inhibitors, which are known to disturb the metabolism of steroid hormones.

摘要

对在16α、17α或17β位带有取代基的雌三烯型和雄甾烷型甾体进行了抑制睾丸酮假单胞菌3β - 羟基甾体氧化还原酶的测试。雌三烯 - 3 - 醇是强效竞争性抑制剂(Ki小于1微摩尔)。雌二醇16α位的取代基对抑制活性有明显影响。17α或17β位的取代基影响较小。3 - 甲氧基雌三烯对酶促3β - OH脱氢没有抑制作用。所测试的4 - 不饱和3 - 氧代甾体是中度抑制剂(Ki为2.4 - 70微摩尔)。活性受17α位取代基的影响较小。10β位取代基按H<CH3<N3的顺序使其活性增加。该抑制试验可用于筛选和排除已知会干扰甾体激素代谢的非常强的合成抑制剂。

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