Demkowicz Sebastian, Kozak Witold, Daśko Mateusz, Masłyk Maciej, Kubiński Konrad, Rachon Janusz
Department of Organic Chemistry, Chemical Faculty, Gdansk University of Technology, Narutowicza 11/12, 80-233, Gdansk, Poland.
Drug Dev Res. 2015 Mar;76(2):94-104. doi: 10.1002/ddr.21245. Epub 2015 Apr 3.
In the present work, we report convenient methods for the synthesis and biological evaluation of phosphate and thiophosphate biphenyl derivatives exhibiting steroid sulfatase (STS) activity. The described synthesis is based on straightforward preparation of biphenyl-4-ol and 4'-hydroxy-biphenyl-4-carboxylic acid ethyl ester modified with various phosphate or thiophosphate moieties. The inhibitory effects of these compounds were tested on STS isolated from human placenta and led to two compounds of interest, 5a and 5d with IC50 values of 28.0 and 22.1 µM, respectively and that had interesting new binding modes in the STS active site.
在本研究中,我们报道了合成和生物学评价具有类固醇硫酸酯酶(STS)活性的磷酸酯和硫代磷酸酯联苯衍生物的简便方法。所描述的合成方法基于直接制备用各种磷酸酯或硫代磷酸酯部分修饰的联苯-4-醇和4'-羟基-联苯-4-羧酸乙酯。测试了这些化合物对从人胎盘中分离出的STS的抑制作用,得到了两种有意义的化合物,5a和5d,其IC50值分别为28.0和22.1 μM,并且它们在STS活性位点具有有趣的新结合模式。