Schimmack W, Lohmann W
Biophys Struct Mech. 1975 Dec 19;1(4):319-28. doi: 10.1007/BF00537645.
The mixed association of testosterone-sulfate and estradiol-sulfate with several derivatives of nucleobases in D2O has been investigated by means of nuclear magnetic resonnance spectroscopy. From the differences among the chemical shifts of the hormone-protons it is concluded, that the nucleobases in the complexes are located above the center of the steroid molecule. The beta-side of the steroid which is characterized by the axial methyl-groups is directed towards the bases. The enthalpies of mixed association of the hormones with a certain nucleobase of the same order of magnitude as the enthalpy of selfassociation of this nucleobase (Schimmack et al., to be published). It is suggested that the complexes are stabilized by van-der-Waals forces. This stacking-like interaction is not specific for the male or female sex hormones: no qualitative or quantitative differences have been observed among the complexes of the two hormone-sulfates with the nucleobases.
通过核磁共振光谱研究了硫酸睾酮和硫酸雌二醇与重水中几种核碱基衍生物的混合缔合。从激素质子化学位移的差异可以得出结论,复合物中的核碱基位于甾体分子中心上方。甾体以轴向甲基为特征的β侧指向碱基。激素与特定核碱基的混合缔合焓与该核碱基自缔合焓处于同一数量级(Schimmack等人,即将发表)。有人认为复合物是通过范德华力稳定的。这种堆积样相互作用对雄性或雌性激素并无特异性:两种硫酸激素与核碱基形成的复合物之间未观察到定性或定量差异。