苦参
雌激素受体
结合亲和力
预酸化
槐花
传统医学
生药学
受体
药理学
医学
生物
化学
生物化学
内科学
生物活性
体外
色谱法
中医药
癌症
病理
酶
替代医学
乳腺癌
苦参碱
作者
Pablo Ibieta Hillerns,Michaël Wink
出处
期刊:Planta Medica
[Georg Thieme Verlag KG]
日期:2005-10-01
卷期号:71 (11): 1065-1068
被引量:38
标识
DOI:10.1055/s-2005-871302
摘要
Prenylflavonoids and lavandulylflavonoids were isolated from the roots of Sophora flavescens Aiton (Fabaceae). The ability of 8-prenylkaempferol (1), kushenol X (2), norkurarinone (3), leachianone A (4), kushenol C (5), maackiain (6) and a root-extract of S. flavescens to displace 17beta-estradiol (E2) from rat uterine estrogen receptor (ER) was determined. Relative binding affinities (RBA) of prenylated flavonoids were weak with RBA values between 0.004 and 0.072. A lavandulyl or prenyl group at the position 8 enhanced binding to rat uterine ER.
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