Morozova T M, Merkulova T I, Martynov V, Iaguzhinskaia V P, Shkodinskaia E N
Eksp Onkol. 1984;6(2):50-4.
The influence of phenestrol and XTJI-51 (hexestrol alkylating derivatives) on uterine tissues and their ability to bind to estrogen receptors were studied. The both compounds studied exhibited estrogenic properties and imitated all effects of estradiol: they increased the uterine wet weight and the activity of thymidine kinase and glucose-6-phosphate dehydrogenase. Although their affinity for estrogen receptors was much weaker than the affinity of estradiol, their complexes with estrogen receptors were more stable than estrogen-receptor complexes.
研究了非尼雌醇和XTJI - 51(己烷雌酚烷基化衍生物)对子宫组织的影响及其与雌激素受体结合的能力。所研究的这两种化合物均表现出雌激素特性,并模拟了雌二醇的所有作用:它们增加了子宫湿重以及胸苷激酶和葡萄糖-6-磷酸脱氢酶的活性。尽管它们对雌激素受体的亲和力远低于雌二醇,但它们与雌激素受体形成的复合物比雌激素-受体复合物更稳定。