Castonguay A, Counsell R E, Skinner R W, Pozderac R V
J Med Chem. 1978 Apr;21(4):391-3. doi: 10.1021/jm00202a015.
A series of substituted 5alpha-androstan-17beta-ols was synthesized and evaluated for their potential use in the development of a prostate imaging agent. The ability of the synthesized compounds to compete with [3H]-5alpha-dihydrotestosterone for rat prostate androgen receptor protein served as the screening assay. For 3-substituted derivatives, the order of binding to the androgen receptor protein was =O greater than -OH greater than H approximately or equal to F. 3beta-Fluoro-5alpha-androstan-17beta-ol was found to have approximately 5% the androgenic activity of testosterone propionate in the castrated rat. The low biological activity for the 3beta-fluoro derivatives, coupled with the synthetic obstacles associated with introducing fluorine-18, has led us to search for more suitable halo steroids as potential radiodiagnostics.
合成了一系列取代的5α-雄甾烷-17β-醇,并对其在前列腺成像剂开发中的潜在用途进行了评估。合成化合物与[3H]-5α-二氢睾酮竞争大鼠前列腺雄激素受体蛋白的能力用作筛选试验。对于3-取代衍生物,与雄激素受体蛋白结合的顺序为=O大于-OH大于H约等于F。发现3β-氟-5α-雄甾烷-17β-醇在去势大鼠中的雄激素活性约为丙酸睾酮的5%。3β-氟衍生物的低生物活性,加上引入氟-18相关的合成障碍,促使我们寻找更合适的卤代甾体作为潜在的放射性诊断剂。