Synthesis and Pharmacological Effects of the Anti-Cancer Agent 2-Methoxyestradiol

被引:19
作者
Solum, Eirik Johansson [1 ]
Akselsen, Oyvind W. [1 ]
Vik, Anders [1 ]
Hansen, Trond Vidar [1 ]
机构
[1] Univ Oslo, Sch Pharm, Dept Pharmaceut Chem, N-0316 Oslo, Norway
关键词
Steroid; 2-methoxyestradiol; anti-cancer effects; anti-vascular effects; anti-angiogenic activities; tubulin inhibition; clinical trials; total synthesis; regioselectivity; INHIBITS TUBULIN POLYMERIZATION; ENDOGENOUS MAMMALIAN METABOLITE; IN-VIVO; BREAST-CANCER; ESTROGEN METABOLITE; ORTHO-FORMYLATION; ORAL; 2-METHOXYESTRADIOL; SUPEROXIDE-DISMUTASE; PHASE-II; A-RING;
D O I
10.2174/1381612821666151002112511
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The endogenous steroid 2-methoxyestradiol (2-ME) is a metabolite of 17 beta-estradiol and its biosynthesis is well established. Moreover, 2-ME is also biosynthesized from estrone. For several years, 2-ME was perceived as an inactive metabolite devoid of any interesting biological activities. Since the late 1980s, a number of biological and pharmacological studies have revealed that 2-ME possesses interesting anti-cancer effects without any undesirable estrogen activity. In particular, the anti-vascular effects and anti-angiogenic activities that 2-ME exhibit, are of great interest and importance, in view of the development of new anti-cancer drugs based on 2-ME. Several clinical trial development programs have been initiated using the steroid 2-ME. In addition, based on the many pharmacological activities reported for 2-ME, but also due to the general interest in total and semi-synthesis of endogenous steroids, several research groups working with organic synthesis have prepared this steroid. Herein, the anti-cancer effects, the results from the clinical trial development programs and the synthetic studies towards 2-ME, are reviewed.
引用
收藏
页码:5453 / 5466
页数:14
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