Gray G O, Leavitt W W
Department of Biochemistry, Texas Tech University Health Sciences Center, Lubbock 79430.
J Steroid Biochem. 1987 Nov;28(5):493-7. doi: 10.1016/0022-4731(87)90507-3.
The biological activity and progestin receptor binding activity of the synthetic steroid RU486 (RU38486; 17-beta-hydroxy-11-beta-(4-dimethylaminophenyl)-17-alpha-(1-propynl++ +)- estra-4,9-diene-3-one) were investigated in the hamster. RU486 demonstrated no antiprogestational activity in the female hamster in that it was ineffective in blocking decidualization or interrupting early pregnancy. Competitive binding assays showed RU486 did not compete from hamster uterine progestin receptor. It is concluded that hamster uterine progestin receptor has unique steroid binding specificity.
在仓鼠中研究了合成甾体RU486(RU38486;17-β-羟基-11-β-(4-二甲基氨基苯基)-17-α-(1-丙炔基)-雌甾-4,9-二烯-3-酮)的生物活性和孕激素受体结合活性。RU486在雌性仓鼠中未表现出抗孕激素活性,因为它在阻断蜕膜化或中断早期妊娠方面无效。竞争性结合试验表明,RU486不能与仓鼠子宫孕激素受体竞争结合。得出的结论是,仓鼠子宫孕激素受体具有独特的甾体结合特异性。