The invention relates to novel estratrienes of general formula (I) containing several sulfamoyoxy groups per molecule (m = 1-5). They are produced by reacting the appropriate steroid alcohols with sulfamoy or n-alkyl or alkanoylsulfamoyl chloride in the presence of a buffer or a base. The compounds of formula (I) an characterized by a high sulfatase activity and are therefore suitable for the treatment of diseases responding to sulfatase inhibition. The high target specificity of the inventive compounds in relation to sulfatase and estrogen transcription assays enable said compounds, which are provided with a radiolabel e.g. [18F] fluorine instead of F. to be used as potential markers in tumor diagnosis.
本发明涉及通式(I)的新型雌
三烯,每个分子含有多个
氨基磺酰基(m = 1-5)。它们是由适当的
甾醇与
氨基磺酰基或正烷基或烷酰
氨基磺酰氯在缓冲液或碱的存在下反应生成的。式(I)化合物的特点是具有较高的
硫酸酯酶活性,因此适用于治疗对
硫酸酯酶抑制有反应的疾病。本发明化合物在
硫酸酯酶和
雌激素转录检测方面具有高度靶向特异性,可作为肿瘤诊断中的潜在标记物。