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新型雌二醇-双膦酸盐缀合物的设计、合成及作为骨靶向雌激素的生物评价。

Design, synthesis, and biological evaluation of novel estradiol-bisphosphonate conjugates as bone-specific estrogens.

机构信息

Medicinal Chemistry Laboratory, Research Division, Mitsubishi-Tanabe Pharma Corporation, 1000 Kamoshida-cho, Aoba-ku, Yokohama 227-0033, Japan.

出版信息

Bioorg Med Chem. 2010 Feb;18(3):1143-8. doi: 10.1016/j.bmc.2009.12.041. Epub 2009 Dec 22.

Abstract

Bone deficiency causes osteoporosis and often decreases quality of life in patients with rheumatoid arthritis. Estrogens are known to protect elderly women from bone loss. Synthesis of new estradiol-bisphosphonate conjugates (E(2)-BPs) was accomplished and their in vivo activity as bone-specific estrogens were examined. Among them, MCC-565 showed selective estrogenic activity in bones; but it showed little estrogenic activity in the uterus. We also found that the linker moiety in E(2)-BPs was essential for the absorption and specificity of the conjugates.

摘要

骨量不足会导致骨质疏松症,并常降低类风湿关节炎患者的生活质量。已知雌激素可防止老年女性骨质流失。我们合成了新型雌二醇-双膦酸盐缀合物(E(2)-BPs),并研究了它们作为骨特异性雌激素的体内活性。其中,MCC-565 在骨骼中表现出选择性雌激素活性,但在子宫中几乎没有雌激素活性。我们还发现 E(2)-BPs 中的连接子部分对于缀合物的吸收和特异性是必需的。

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