Amr Abd El-Galil E, Abdel-Latif Nehad A, Abdalla Mohamed M
Applied Organic Chemistry Department, National Research Centre, Dokki, Cairo, Egypt.
Bioorg Med Chem. 2006 Jan 15;14(2):373-84. doi: 10.1016/j.bmc.2005.08.024. Epub 2005 Sep 22.
A series of androstano[17,16-c]pyrazolines and their oxidized derivatives (2-14) were synthesized using 3beta-hydroxyandrostan-17-one as a starting material (1a, b). The synthesized compounds were evaluated for their antiandrogenic activity compared to that of Cyproterone as positive control. Some of the compounds exhibited better antiandrogenic activity than the reference drug. The detailed synthesis, spectroscopic data, ED(50), and toxicity (LD(50) and LD(90)) of the synthesized compounds were reported.
以3β-羟基雄甾-17-酮(1a,b)为起始原料,合成了一系列雄甾烷[17,16-c]吡唑啉及其氧化衍生物(2-14)。将合成的化合物与作为阳性对照的醋酸环丙孕酮相比,评估其抗雄激素活性。一些化合物表现出比参比药物更好的抗雄激素活性。报道了合成化合物的详细合成方法、光谱数据、半数有效剂量(ED(50))以及毒性(半数致死剂量(LD(50))和90%致死剂量(LD(90)))。