The present invention relates to substituted arylsulphonylaminomethyl-phosphonic acid derivatives of general formula
wherein R, X, Y and Z are defined as in claim
1
, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the G
L
subunit of glycogen-associated protein phosphatase 1 (PP1), and their use as pharmaceutical compositions.
本发明涉及一种一般式为R,X,Y和Z如权利要求1所定义的取代芳基磺酰
氨甲基膦酸衍
生物,其互变异构体,对映异构体,对映体混合物和盐具有有价值的药理学特性,特别是抑制
糖原磷酸化酶a与
糖原相关蛋白
磷酸酶1(PP1)的GL亚单位的相互作用,并将其用作制药组合物。