CAJ | 학술논문

目的为寻找高效低毒的雌激素受体拮抗剂，设计合成了新结构骨架的三苯乙烯类化合物。方法通过McMurry反应得到三苯乙烯中间体，再经醚化反应得到目的物。通过抗小鼠子宫增重实验测定化合物的拮抗活性，竞争性结合雌激素受体实验测定化合物对受体的亲和力。结果本文共合成了35个新化学实体，并利用X-射线晶体衍射和氢谱确定了化合物的构型。结论所有化合物均能与受体结合(IC50<10-6 mol.L-1)，其中化合物35与受体的亲和力最大。某些化合物抑制子宫的增长，表现为拮抗作用；有的则促进子宫的增长，表现为激动作用。其中化合物14和27对子宫的抑制作用强于或相当于他莫昔芬，有待进一步研究。
목적위심조고효저독적자격소수체길항제，설계합성료신결구골가적삼분을희류화합물。방법통과McMurry반응득도삼분을희중간체，재경미화반응득도목적물。통과항소서자궁증중실험측정화합물적길항활성，경쟁성결합자격소수체실험측정화합물대수체적친화력。결과본문공합성료35개신화학실체，병이용X-사선정체연사화경보학정료화합물적구형。결론소유화합물균능여수체결합(IC50<10-6 mol.L-1)，기중화합물35여수체적친화력최대。모사화합물억제자궁적증장，표현위길항작용；유적칙촉진자궁적증장，표현위격동작용。기중화합물14화27대자궁적억제작용강우혹상당우타막석분，유대진일보연구。
AIM　In order to improve the biological activity and reduce the side effects and toxicity, a series of novel estrogen receptor antagonists were designed. METHODS　The key triphenylethylene intermediates were obtained by the McMurry reaction. The target compounds were prepared by etherification. The binding affinities of the target compounds for the estrogen receptor in rat uterine cytosol were measured by a competitive binding assay and their estrogen agonistic/antagonistic properties were investigated in the 3-day uterine weight assay in the immature rats. RESULTS　Thirty-five new compounds have been synthesized and their geometric configuration were determined by X-ray crystallography and 1HNMR spectral data. CONCLUSION　All of the test compounds showed affinity for the estrogen receptor (IC50<10-6 mol.L-1), especially compound 35 with IC50 1.07×10-8 mol.L-1. Some compounds are antagonists, inhibiting uterus growth; others are agonists, promoting uterus growth. Compounds 14 and 27 are superior antagonists to tamoxifen.