We report the synthesis, evaluation and rationalisation of the inhibitory activity of a series of 3,5-dibromo
derivatives of 4-hydroxyphenyl ketone as probes of the active site of the type 3 of 17β-hydroxysteroid dehydrogenase
(17β-HSD3). The results support the important role of hydrogen bonding interaction in the inhibition of 17β-HSD3.
我们报告了系列3,5-二
溴-
4-羟基苯基酮衍
生物的合成、评价及其抑制活性的合理化,这些化合物作为17β-羟基类
固醇脱氢酶(17β-H
SD3)第三类活性位点的探针。结果支持了氢键相互作用在抑制17β-H
SD3中的重要作用。